Idiopathic interstitial pneumonia pathophysiology: Difference between revisions

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__NOTOC__
__NOTOC__
{{SI}}
{{Idiopathic interstitial pneumonia}}
{{CMG}}; {{AE}} {{chetan}}
{{CMG}}; {{AE}} {{chetan}}


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==Overview==
==Overview==
Idiopathic interstitial pneumonia (IIP) is a disease entity that can be histologically classified into different categories.  [[Idiopathic pulmonary fibrosis]] has the same features as that of usual interstitial pneumonia (UIP) whereas no specific pattern or common feature is noted among the other types of IIP.  The pathophysiology of IIP can be summarized in the following three stages: recruitment of inflammatory cells, abnormal [[collagen]] deposition and fibroblastic proliferation and lastly progression to [[fibrosis]].


==Pathophysiology==
==Pathophysiology==
===[[Idiopathic pulmonary fibrosis]]===
===Idiopathic Pulmonary Fibrosis===
Idiopathic pulmonary fibrosis (IPF) has often been considered an [[autoimmunity|autoimmune disease]].  However, it is perhaps better characterized as an abnormal and excessive deposition of fibrotic tissue in the pulmonary interstitium with minimal associated [[inflammation]].<ref name="Selman">{{cite journal |last=Selman |first=Moisés |coauthors=Talmadge E. King, Jr.; and Annie Pardo |title=Idiopathic pulmonary fibrosis: prevailing and evolving hypotheses about its pathogenesis and implications for therapy |journal=Annals of Internal Medicine |year=2001 |volume=134 |number=2 |pages=136-51|url=http://www.annals.org/cgi/content/abstract/134/2/136}}</ref> [[Autoantibodies]], a hallmark of autoimmune diseases, are found in a minority of patients with true idiopathic pulmonary fibrosis.  Moreover, many autoimmune diseases that are associated with pulmonary fibrosis such as [[scleroderma]], are more frequently associated with a related but more inflammatory disease, nonspecific interstitial pneumonitis.<ref>{{cite journal |last=King, Jr. |first=Talmadge E. |title=Centennial review: clinical advances in the diagnosis and therapy of the interstitial lung diseases|url=http://ajrccm.atsjournals.org/cgi/content/full/172/3/268 |journal=American Journal of Respiratory and Critical Care Medicine |year=2005 |volume=172 |number=3 |pages=268-79}}</ref> IPF is associated with [[smoking]]<ref>{{cite journal |last=Nagai |first=Sonoko |coauthors=Yuma Hoshino, Michio Hayashi, Isao Ito |title=Smoking-related interstitial lung diseases |url=http://www.co-pulmonarymedicine.com/pt/re/copulmonary/abstract.00063198-200009000-00005.htm |journal=Current Opinion in Pulmonary Medicine |volume=6 |issue=5 |pages=415-9 |year=2000 |pmid=10958232}}</ref> and exhibits some dependency on the amount of smoking.<ref>{{cite journal |last=Baumgartner |first=KB |coauthors=Samet JM, Stidley CA, Colby TV, Waldron JA |title=Cigarette smoking: a risk factor for idiopathic pulmonary fibrosis |url= http://ajrccm.atsjournals.org/cgi/content/short/155/1/242 |journal=American Journal of Respiratory and Critical Care Medicine |volume=155 |number=1 |pages=242-248 |year=1997 |pmid=9001319}}</ref>


Pulmonary fibrosis has often been called an [[autoimmunity|autoimmune disease]]. However, it is perhaps better characterized as an abnormal and excessive deposition of fibrotic tissue in the pulmonary interstitium with minimal associated inflammation.<ref name="Selman">{{cite journal |last=Selman |first=Moisés |coauthors=Talmadge E. King, Jr.; and Annie Pardo |title=Idiopathic pulmonary fibrosis: prevailing and evolving hypotheses about its pathogenesis and implications for therapy |journal=Annals of Internal Medicine |year=2001 |volume=134 |number=2 |pages=136-51|url=http://www.annals.org/cgi/content/abstract/134/2/136}}</ref> [[Autoantibodies]], a hallmark of autoimmune diseases, are found in a minority of patients with truly idiopathic pulmonary fibrosis. Moreover, many autoimmune diseases associated with "pulmonary fibrosis", such as scleroderma, are more frequently associated with a related but more inflammatory disease, nonspecific interstitial pneumonitis.<ref>{{cite journal |last=King, Jr. |first=Talmadge E. |title=Centennial review: clinical advances in the diagnosis and therapy of the interstitial lung diseases|url=http://ajrccm.atsjournals.org/cgi/content/full/172/3/268 |journal=American Journal of Respiratory and Critical Care Medicine |year=2005 |volume=172 |number=3 |pages=268-79}}</ref> It is associated with[[smoking]]<ref>{{cite journal |last=Nagai |first=Sonoko |coauthors=Yuma Hoshino, Michio Hayashi, Isao Ito |title=Smoking-related interstitial lung diseases |url=http://www.co-pulmonarymedicine.com/pt/re/copulmonary/abstract.00063198-200009000-00005.htm |journal=Current Opinion in Pulmonary Medicine |volume=6 |issue=5 |pages=415-9 |year=2000 |pmid=10958232}}</ref> and exhibits some dependency on the amount of smoking.<ref>{{cite journal |last=Baumgartner |first=KB |coauthors=Samet JM, Stidley CA, Colby TV, Waldron JA |title=Cigarette smoking: a risk factor for idiopathic pulmonary fibrosis |url= http://ajrccm.atsjournals.org/cgi/content/short/155/1/242 |journal=American Journal of Respiratory and Critical Care Medicine |volume=155 |number=1 |pages=242-248 |year=1997 |pmid=9001319}}</ref>


===Idiopathic Non-specific Interstitial Pneumonia (NSIP)===
Shown below is an image depicting IPF:


There are some common associations between NSIP and usual interstitial pneumonia (UIP). Histologically patients can manifest lesions of UIP and NSIP simultaneously.<ref name="Monaghan-2004">{{Cite journal | last1 = Monaghan | first1 = H. | last2 = Wells | first2 = AU. | last3 = Colby | first3 = TV. | last4 = du Bois | first4 = RM. | last5 = Hansell | first5 = DM. | last6 = Nicholson | first6 = AG. | title = Prognostic implications of histologic patterns in multiple surgical lung biopsies from patients with idiopathic interstitial pneumonias. | journal = Chest | volume = 125 | issue = 2 | pages = 522-6 | month = Feb | year = 2004 | doi = | PMID = 14769733 }}</ref><ref name="Flaherty-2001">{{Cite journal | last1 = Flaherty | first1 = KR. | last2 = Travis | first2 = WD. | last3 = Colby | first3 = TV. | last4 = Toews | first4 = GB. | last5 = Kazerooni | first5 = EA. | last6 = Gross | first6 = BH. | last7 = Jain | first7 = A. | last8 = Strawderman | first8 = RL. | last9 = Flint | first9 = A. | title = Histopathologic variability in usual and nonspecific interstitial pneumonias. | journal = Am J Respir Crit Care Med | volume = 164 | issue = 9 | pages = 1722-7 | month = Nov | year = 2001 | doi = 10.1164/ajrccm.164.9.2103074 | PMID = 11719316 }}</ref> Some common factors include exposures, genetic mutations. Exact cause and nature is still unknown.
[[File:Journal.pmed.0020314.g001 Osteopontin .png|300px|Idiopathic Pulmonary Fibrosis]]


Recent studies conclude that epithelial injury and dysregulated repair play a major role.<ref name="Ishii-">{{Cite journal | last1 = Ishii | first1 = H. | last2 = Mukae | first2 = H. | last3 = Kadota | first3 = J. | last4 = Fujii | first4 = T. | last5 = Abe | first5 = K. | last6 = Ashitani | first6 = J. | last7 = Kohno | first7 = S. | title = Increased levels of interleukin-18 in bronchoalveolar lavage fluid of patients with idiopathic nonspecific interstitial pneumonia. | journal = Respiration | volume = 72 | issue = 1 | pages = 39-45 | month = | year = | doi = 10.1159/000083399 | PMID = 15753633 }}</ref> [[Cytokines]] and some proteins like epimorphin (a cell surface associated protein), matrix metalloproteinases, heat shock protein, surfactant protein C, the coagulation system, intercellular adhesion molecules-1, IL-4, IL-13, IL-18, interferon-gamma, pro fibrotic chemokine, CCL7, and CCL5.<ref name="Terasaki-2000">{{Cite journal | last1 = Terasaki | first1 = Y. | last2 = Fukuda | first2 = Y. | last3 = Ishizaki | first3 = M. | last4 = Yamanaka | first4 = N. | title = Increased expression of epimorphin in bleomycin-induced pulmonary fibrosis in mice. | journal = Am J Respir Cell Mol Biol | volume = 23 | issue = 2 | pages = 168-74 | month = Aug | year = 2000 | doi = 10.1165/ajrcmb.23.2.3973 | PMID = 10919982 }}</ref><ref name="Suga-2000">{{Cite journal | last1 = Suga | first1 = M. | last2 = Iyonaga | first2 = K. | last3 = Okamoto | first3 = T. | last4 = Gushima | first4 = Y. | last5 = Miyakawa | first5 = H. | last6 = Akaike | first6 = T. | last7 = Ando | first7 = M. | title = Characteristic elevation of matrix metalloproteinase activity in idiopathic interstitial pneumonias. | journal = Am J Respir Crit Care Med | volume = 162 | issue = 5 | pages = 1949-56 | month = Nov | year = 2000 | doi = 10.1164/ajrccm.162.5.9906096 | PMID = 11069839 }}</ref><ref name="Kakugawa-2005">{{Cite journal | last1 = Kakugawa | first1 = T. | last2 = Mukae | first2 = H. | last3 = 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205-11 | month = Aug | year = 2001 | doi = | PMID = 11512562 }}</ref><ref name="Jakubzick-2004">{{Cite journal | last1 = Jakubzick | first1 = C. | last2 = Choi | first2 = ES. | last3 = Kunkel | first3 = SL. | last4 = Evanoff | first4 = H. | last5 = Martinez | first5 = FJ. | last6 = Puri | first6 = RK. | last7 = Flaherty | first7 = KR. | last8 = Toews | first8 = GB. | last9 = Colby | first9 = TV. | title = Augmented pulmonary IL-4 and IL-13 receptor subunit expression in idiopathic interstitial pneumonia. | journal = J Clin Pathol | volume = 57 | issue = 5 | pages = 477-86 | month = May | year = 2004 | doi = | PMID = 15113854 }}</ref><ref name="Keogh-2005">{{Cite journal | last1 = Keogh | first1 = KA. | last2 = Limper | first2 = AH. | title = Characterization of lymphocyte populations in nonspecific interstitial pneumonia. | journal = Respir Res | volume = 6 | issue = | pages = 137 | month = | year = 2005 | doi = 10.1186/1465-9921-6-137 | PMID = 16287509 }}</ref><ref name="Choi-2004">{{Cite journal | last1 = Choi | first1 = ES. | last2 = Jakubzick | first2 = C. | last3 = Carpenter | first3 = KJ. | last4 = Kunkel | first4 = SL. | last5 = Evanoff | first5 = H. | last6 = Martinez | first6 = FJ. | last7 = Flaherty | first7 = KR. | last8 = Toews | first8 = GB. | last9 = Colby | first9 = TV. | title = Enhanced monocyte chemoattractant protein-3/CC chemokine ligand-7 in usual interstitial pneumonia. | journal = Am J Respir Crit Care Med | volume = 170 | issue = 5 | pages = 508-15 | month = Sep | year = 2004 | doi = 10.1164/rccm.200401-002OC | PMID = 15191918 }}</ref> A bronchoalveloar lavage (BAL) revealed the presence of lymphocytes in the alveolar septum, which suggests the involvement of the immune system.<ref name="Cottin-1998">{{Cite journal | last1 = Cottin | first1 = V. | last2 = Donsbeck | first2 = AV. | last3 = Revel | first3 = D. | last4 = Loire | first4 = R. | last5 = Cordier | first5 = JF. | title = Nonspecific interstitial pneumonia. Individualization of a clinicopathologic entity in a series of 12 patients. | journal = Am J Respir Crit Care Med | volume = 158 | issue = 4 | pages = 1286-93 | month = Oct | year = 1998 | doi = 10.1164/ajrccm.158.4.9802119 | PMID = 9769293 }}</ref><ref name="Fujita-1999">{{Cite journal | last1 = Fujita | first1 = J. | last2 = Yamadori | first2 = I. | last3 = Suemitsu | first3 = I. | last4 = Yoshinouchi | first4 = T. | last5 = Ohtsuki | first5 = Y. | last6 = Yamaji | first6 = Y. | last7 = Kamei | first7 = T. | last8 = Kobayashi | first8 = M. | last9 = Nakamura | first9 = Y. | title = Clinical features of non-specific interstitial pneumonia. | journal = Respir Med | volume = 93 | issue = 2 | pages = 113-8 | month = Feb | year = 1999 | doi = | PMID = 10464862 }}</ref><ref name="Nagai-1998">{{Cite journal | last1 = Nagai | first1 = S. | last2 = Kitaichi | first2 = M. | last3 = Itoh | first3 = H. | last4 = Nishimura | first4 = K. | last5 = Izumi | first5 = T. | last6 = Colby | first6 = TV. | title = Idiopathic nonspecific interstitial pneumonia/fibrosis: comparison with idiopathic pulmonary fibrosis and BOOP. | journal = Eur Respir J | volume = 12 | issue = 5 | pages = 1010-9 | month = Nov | year = 1998 | doi = | PMID = 9863989 }}</ref><ref name="Park-1996">{{Cite journal | last1 = Park | first1 = CS. | last2 = Jeon | first2 = JW. | last3 = Park | first3 = SW. | last4 = Lim | first4 = GI. | last5 = Jeong | first5 = SH. | last6 = Uh | first6 = ST. | last7 = Park | first7 = JS. | last8 = Choi | first8 = DL. | last9 = Jin | first9 = SY. | title = Nonspecific interstitial pneumonia/fibrosis: clinical manifestations, histologic and radiologic features. | journal = Korean J Intern Med | volume = 11 | issue = 2 | pages = 122-32 | month = Jun | year = 1996 | doi = | PMID = 8854648 }}</ref>A greater number of [[dendritic cells]] (DC), which help in antigen presentation, are visualized in close association to [[CD4]] and [[CD8]] lymphocytes in biopsy in NSIS patients than UIP .<ref name="Shimizu-2002">{{Cite journal | last1 = Shimizu | first1 = S. | last2 = Yoshinouchi | first2 = T. | last3 = Ohtsuki | first3 = Y. | last4 = Fujita | first4 = J. | last5 = Sugiura | first5 = Y. | last6 = Banno | first6 = S. | last7 = Yamadori | first7 = I. | last8 = Eimoto | first8 = T. | last9 = Ueda | first9 = R. | title = The appearance of S-100 protein-positive dendritic cells and the distribution of lymphocyte subsets in idiopathic nonspecific interstitial pneumonia. | journal = Respir Med | volume = 96 | issue = 10 | pages = 770-6 | month = Oct | year = 2002 | doi = | PMID = 12412975 }}</ref>[[Fibroblasts]] are key pathological cells involved in fibrotic lung diseases.<ref name="Selman-2001">{{Cite journal | last1 = Selman | first1 = M. | last2 = King | first2 = TE. | last3 = Pardo | first3 = A. | title = Idiopathic pulmonary fibrosis: prevailing and evolving hypotheses about its pathogenesis and implications for therapy. | journal = Ann Intern Med | volume = 134 | issue = 2 | pages = 136-51 | month = Jan | year = 2001 | doi = | PMID = 11177318 }}</ref>Fibroblasts secreting transforming growth factor–Beta (TGF-β) and fibronectin are the differentiating characters in NSIS and UIP.<ref name="Miki-2000">{{Cite journal | last1 = Miki | first1 = H. | last2 = Mio | first2 = T. | last3 = Nagai | first3 = S. | last4 = Hoshino | first4 = Y. | last5 = Nagao | first5 = T. | last6 = Kitaichi | first6 = M. | last7 = Izumi | first7 = T. | title = Fibroblast contractility: usual interstitial pneumonia and nonspecific interstitial pneumonia. | journal = Am J Respir Crit Care Med | volume = 162 | issue = 6 | pages = 2259-64 | month = Dec | year = 2000 | doi = 10.1164/ajrccm.162.6.9812029 | PMID = 11112149 }}</ref>
===Idiopathic Non-specific Interstitial Pneumonia ===
As the name implies, idiopathic non-specific interstitial pneumonia (NSIP) has very inconsistent and non-specific findings.<ref name="Flaherty-2001">{{Cite journal | last1 = Flaherty | first1 = KR. | last2 = Travis | first2 = WD. | last3 = Colby | first3 = TV. | last4 = Toews | first4 = GB. | last5 = Kazerooni | first5 = EA. | last6 = Gross | first6 = BH. | last7 = Jain | first7 = A. | last8 = Strawderman | first8 = RL. | last9 = Flint | first9 = A. | title = Histopathologic variability in usual and nonspecific interstitial pneumonias. | journal = Am J Respir Crit Care Med | volume = 164 | issue = 9 | pages = 1722-7 | month = Nov | year = 2001 | doi = 10.1164/ajrccm.164.9.2103074 | PMID = 11719316 }}</ref><ref name="Cottin-1998">{{Cite journal | last1 = Cottin | first1 = V. | last2 = Donsbeck | first2 = AV. | last3 = Revel | first3 = D. | last4 = Loire | first4 = R. | last5 = Cordier | first5 = JF. | title = Nonspecific interstitial pneumonia. Individualization of a clinicopathologic entity in a series of 12 patients. | journal = Am J Respir Crit Care Med | volume = 158 | issue = 4 | pages = 1286-93 | month = Oct | year = 1998 | doi = 10.1164/ajrccm.158.4.9802119 | PMID = 9769293 }}</ref><ref name="Katzenstein-2000">{{Cite journal | last1 = Katzenstein | first1 = AL. | last2 = Myers | first2 = JL. | title = Nonspecific interstitial pneumonia and the other idiopathic interstitial pneumonias: classification and diagnostic criteria. | journal = Am J Surg Pathol | volume = 24 | issue = 1 | pages = 1-3 | month = Jan | year = 2000 | doi = | PMID = 10632482 }}</ref>
Changes similar to other cases of interstitial pneumonia are seen which are migration of inflammatory cells in the alveolar septa and its widening with or without fibrosis.
NSIP can be divided into three groups based on histopathological changes.<ref name="Katzenstein-1994">{{Cite journal | last1 = Katzenstein | first1 = AL. | last2 = Fiorelli | first2 = RF. | title = Nonspecific interstitial pneumonia/fibrosis. Histologic features and clinical significance. | journal = Am J Surg Pathol | volume = 18 | issue = 2 | pages = 136-47 | month = Feb | year = 1994 | doi = | PMID = 8291652 }}</ref> Shown below is a table summarizing the pathological findings in the three groups of NSIP:
{| {{table}}
| align="center" style="background:#f0f0f0" | '''Stage'''
| align="center" style="background:#f0f0f0 " | '''Pathological Feature '''
|-
| Group I || Inflammatory cells predominant stage
|-
| Group II|| Accompanying fibrosis
|-
| Group III|| Fibrosis prevalent


|-
|}


===Respiratory Bronchiolitis-Interstitial Lung Disease (RB-ILD)===
Bronchoalveloar lavage (BAL) reveals the presence of [[lymphocytes]] in the alveolar septum which is an evidence of the involvement of the immune system.<ref name="Cottin-1998">{{Cite journal | last1 = Cottin | first1 = V. | last2 = Donsbeck | first2 = AV. | last3 = Revel | first3 = D. |last4 = Loire | first4 = R. | last5 = Cordier | first5 = JF. | title = Nonspecific interstitial pneumonia. Individualization of a clinicopathologic entity in a series of 12 patients. | journal = Am J Respir Crit Care Med | volume = 158 | issue = 4 | pages = 1286-93 | month = Oct | year = 1998 | doi = 10.1164/ajrccm.158.4.9802119 | PMID = 9769293 }}</ref><ref name="Fujita-1999">{{Cite journal | last1 = Fujita |first1 = J. | last2 = Yamadori | first2 = I. | last3 = Suemitsu | first3 = I. | last4 = Yoshinouchi | first4 = T. | last5 = Ohtsuki | first5 = Y. | last6 = Yamaji | first6 = Y. | last7 = Kamei | first7 = T. |last8 = Kobayashi | first8 = M. | last9 = Nakamura | first9 = Y. | title = Clinical features of non-specific interstitial pneumonia. | journal = Respir Med | volume = 93 | issue = 2 | pages = 113-8 | month = Feb | year = 1999 | doi = | PMID = 10464862 }}</ref><ref name="Nagai-1998">{{Cite journal | last1 = Nagai | first1 = S. | last2 = Kitaichi | first2 = M. | last3 = Itoh | first3 = H. | last4 = Nishimura |first4 = K. | last5 = Izumi | first5 = T. | last6 = Colby | first6 = TV. | title = Idiopathic nonspecific interstitial pneumonia/fibrosis: comparison with idiopathic pulmonary fibrosis and BOOP. | journal = Eur Respir J | volume = 12 | issue = 5 | pages = 1010-9 | month = Nov | year = 1998 | doi = | PMID = 9863989 }}</ref><ref name="Park-1996">{{Cite journal | last1 = Park | first1 = CS. | last2 = Jeon | first2 = JW. | last3 = Park | first3 = SW. | last4 = Lim | first4 = GI. | last5 = Jeong | first5 = SH. | last6 = Uh | first6 = ST. | last7 = Park | first7 = JS. | last8 = Choi | first8 = DL. | last9 = Jin | first9 = SY. | title = Nonspecific interstitial pneumonia/fibrosis: clinical manifestations, histologic and radiologic features. | journal = Korean J Intern Med | volume = 11 | issue = 2 | pages = 122-32 | month = Jun| year = 1996 | doi = | PMID = 8854648 }}</ref>
A greater number of [[dendritic cells]] (DC), which help in antigen presentation, are visualized in close association with [[CD4]] and [[CD8]] lymphocytes in the biopsy of NSIS patients than in UIP.<ref name="Shimizu-2002">{{Cite journal | last1 = Shimizu | first1 = S. | last2 = Yoshinouchi | first2 = T. | last3 = Ohtsuki | first3 = Y. | last4 = Fujita | first4 = J. |last5 = Sugiura | first5 = Y. | last6 = Banno | first6 = S. | last7 = Yamadori | first7 = I. | last8 = Eimoto | first8 = T. | last9 = Ueda | first9 = R. | title = The appearance of S-100 protein-positive dendritic cells and the distribution of lymphocyte subsets in idiopathic nonspecific interstitial pneumonia. | journal = Respir Med | volume = 96 | issue = 10 | pages = 770-6 | month = Oct | year = 2002 | doi = | PMID = 12412975 }}</ref>
[[Fibroblasts]] are the key cells involved in fibrotic lung diseases.<ref name="Selman-2001">{{Cite journal | last1 = Selman | first1 = M. | last2 = King | first2 = TE. |last3 = Pardo | first3 = A. | title = Idiopathic pulmonary fibrosis: prevailing and evolving hypotheses about its pathogenesis and implications for therapy. | journal = Ann Intern Med | volume = 134 | issue = 2 | pages = 136-51 | month = Jan | year = 2001 | doi = | PMID = 11177318 }}</ref>


[[Cigarette smoking]] could be one of the major causative agent of RB-ILD.Some radiologic studies may show a relation between the duration and the intensity of cigarette smoking and visualization of opacities on chest radiographs which could be associated to RB-ILD.<ref name="Carilli-1973">{{Cite journal | last1 = Carilli | first1 = AD. | last2 = Kotzen | first2 = LM. | last3 = Fischer | first3 = MJ. | title = The chest roentgenogram in smoking females. | journal = Am Rev Respir Dis | volume = 107 | issue = 1 | pages = 133-6 | month = Jan | year = 1973 | doi = | PMID = 4683317 }}</ref><ref name="Weiss-1984">{{Cite journal | last1 = Weiss | first1 = W. | title = Cigarette smoke, asbestos, and small irregular opacities. | journal = Am Rev Respir Dis | volume = 130 | issue = 2 | pages = 293-301 | month = Aug | year = 1984 | doi = | PMID = 6380358 }}</ref><ref name="Weiss-1991">{{Cite journal | last1 = Weiss | first1 = W. | title = Cigarette smoking and small irregular opacities. | journal = Br J Ind Med | volume = 48 | issue = 12 | pages = 841-4 | month = Dec | year = 1991 | doi = | PMID = 1772799 }}</ref><ref name="Dick-1992">{{Cite journal | last1 = Dick | first1 = JA. | last2 = Morgan | first2 = WK. | last3 = Muir | first3 = DF. | last4 = Reger | first4 = RB. | last5 = Sargent | first5 = N. | title = The significance of irregular opacities on the chest roentgenogram. | journal = Chest | volume = 102 | issue = 1 | pages = 251-60 | month = Jul | year = 1992 | doi = | PMID = 1623762 }}</ref>As the name suggests the pathology is in the bronchiole. It’s a more centrally distributed pathology especially in the lumen though the bronchioles, alveolar ducts and the peribronchiolar alveolar spaces may show clusters of macrophages which are dusty and brown.<ref name="Myers-1987">{{Cite journal | last1 = Myers | first1 = JL. | last2 = Veal | first2 = CF. | last3 = Shin | first3 = MS. | last4 = Katzenstein | first4 = AL. | title = Respiratory bronchiolitis causing interstitial lung disease. A clinicopathologic study of six cases. | journal = Am Rev Respir Dis | volume = 135 | issue = 4 | pages = 880-4 | month = Apr | year = 1987 | doi = | PMID = 3565934 }}</ref><ref name="Yousem-1989">{{Cite journal | last1 = Yousem | first1 = SA. | last2 = Colby | first2 = TV. | last3 = Gaensler | first3 = EA. | title = Respiratory bronchiolitis-associated interstitial lung disease and its relationship to desquamative interstitial pneumonia. | journal = Mayo Clin Proc | volume = 64 | issue = 11 | pages = 1373-80 | month = Nov | year = 1989 | doi = | PMID = 2593722 }}</ref><ref name="Niewoehner-1974">{{Cite journal | last1 = Niewoehner | first1 = DE. | last2 = Kleinerman | first2 = J. | last3 = Rice | first3 = DB. | title = Pathologic changes in the peripheral airways of young cigarette smokers. | journal = N Engl J Med | volume = 291 | issue = 15 | pages = 755-8 | month = Oct | year = 1974 | doi = 10.1056/NEJM197410102911503 | PMID = 4414996 }}</ref><ref name="Churg-2010">{{Cite journal | last1 = Churg | first1 = A. | last2 = Müller | first2 = NL. | last3 = Wright | first3 = JL. | title = Respiratory bronchiolitis/interstitial lung disease: fibrosis, pulmonary function, and evolving concepts. | journal = Arch Pathol Lab Med | volume = 134 | issue = 1 | pages = 27-32 | month = Jan | year = 2010 | doi = 10.1043/1543-2165-134.1.27 | PMID = 20073602 }}</ref><ref name="Cosio-1980">{{Cite journal | last1 = Cosio | first1 = MG. | last2 = Hale | first2 = KA. | last3 = Niewoehner | first3 = DE. | title = Morphologic and morphometric effects of prolonged cigarette smoking on the small airways. | journal = Am Rev Respir Dis | volume = 122 | issue = 2 | pages = 265-21 | month = Aug | year = 1980 | doi = | PMID = 7416603 }}</ref><ref name="Colby-1998">{{Cite journal | last1 = Colby | first1 = TV. | title = Bronchiolitis. Pathologic considerations. | journal = Am J Clin Pathol | volume = 109 | issue = 1 | pages = 101-9 | month = Jan | year = 1998 | doi = | PMID = 9426525 }}</ref> Granular golden brown particles having plenty of cytoplasm may be seen. These particles are PAS-positive and Prussian blue –positive which implies increased iron content in alveolar macrophage, which might be associated to smoking.<ref name="Niewoehner-1974">{{Cite journal | last1 = Niewoehner | first1 = DE. | last2 = Kleinerman | first2 = J. | last3 = Rice | first3 = DB. | title = Pathologic changes in the peripheral airways of young cigarette smokers. | journal = N Engl J Med | volume = 291 | issue = 15 | pages = 755-8 | month = Oct | year = 1974 | doi = 10.1056/NEJM197410102911503 | PMID = 4414996 }}</ref><ref name="Cosio-1980">{{Cite journal | last1 = Cosio | first1 = MG. | last2 = Hale | first2 = KA. | last3 = Niewoehner | first3 = DE. | title = Morphologic and morphometric effects of prolonged cigarette smoking on the smallairways. | journal = Am Rev Respir Dis | volume = 122 | issue = 2 | pages = 265-21 | month = Aug | year = 1980 | doi = | PMID = 7416603 }}</ref><ref name="Churg-2010">{{Cite journal | last1 = Churg | first1 = A. | last2 = Müller | first2 = NL. | last3 = Wright | first3 = JL. | title = Respiratory bronchiolitis/interstitial lung disease: fibrosis, pulmonary function, and evolving concepts. | journal = Arch Pathol Lab Med | volume = 134 | issue = 1 | pages = 27-32 | month = Jan | year = 2010 | doi = 10.1043/1543-2165-134.1.27 | PMID = 20073602 }}</ref>
The pathological mechanism of NSIP involves:
A common appearance between DIP and respiratory bronchiolitis would be a combination of alveolar septal thickening, epithelial hyperplasia and pigmented macrophages in the lumen. There are lymphocytes and histiocytes present in an irregular way in the submucosa. Similar to the black pigment in the [[macrophage]] a dark black anthracotic pigment is what could be seen in the histiocytes.<ref name="Yousem-1989">{{Cite journal | last1 = Yousem | first1 = SA. | last2 = Colby | first2 = TV. | last3 = Gaensler | first3 = EA. | title = Respiratory bronchiolitis-associated interstitial lung disease and its relationship to desquamative interstitial pneumonia. | journal = Mayo Clin Proc | volume = 64 | issue = 11 | pages = 1373-80 | month = Nov | year = 1989 | doi = | PMID = 2593722 }}</ref><ref name="Colby-1998">{{Cite journal | last1 = Colby | first1 = TV. | title = Bronchiolitis. Pathologic considerations. | journal = Am J Clin Pathol | volume = 109 | issue = 1 | pages = 101-9 | month = Jan | year = 1998 | doi = | PMID = 9426525 }}</ref> Type 2 hyerplastic cells and cuboidal bronchiolar type epithelium could be seen lining the peribronchiolar fibrosis.
:* Epithelial injury and dysregulated repair (major role)<ref name="Ishii-">{{Cite journal | last1 = Ishii | first1 = H. | last2 = Mukae | first2 = H. | last3 = Kadota | first3 = J. | last4 = Fujii |first4 = T. | last5 = Abe | first5 = K. | last6 = Ashitani | first6 = J. | last7 = Kohno | first7 = S. | title = Increased levels of interleukin-18 in bronchoalveolar lavage fluid of patients with idiopathic nonspecific interstitial pneumonia. | journal = Respiration | volume = 72 | issue = 1 | pages = 39-45 | month = | year = | doi = 10.1159/000083399 | PMID = 15753633 }}</ref>
:*[[Cytokines]]
:*Proteins like epimorphin (a cell surface associated protein)<ref name="Terasaki-2000">{{Cite journal | last1 = Terasaki | first1 = Y. |last2 = Fukuda | first2 = Y. | last3 = Ishizaki | first3 = M. | last4 = Yamanaka | first4 = N. | title = Increased expression of epimorphin in bleomycin-induced pulmonary fibrosis in mice. | journal = Am J Respir Cell Mol Biol | volume = 23 | issue = 2 | pages = 168-74 | month = Aug | year = 2000 | doi = 10.1165/ajrcmb.23.2.3973 | PMID = 10919982 }}</ref>   [[matrix metalloproteinases]],<ref name="Suga-2000">{{Cite journal | last1 = Suga |first1 = M. | last2 = Iyonaga | first2 = K. | last3 = Okamoto | first3 = T. | last4 = Gushima | first4 = Y. | last5 = Miyakawa | first5 = H. | last6 = Akaike | first6 = T. | last7 = Ando | first7 = M. | title = Characteristic elevation of matrix metalloproteinase activity in idiopathic interstitial pneumonias. | journal = Am J Respir Crit Care Med | volume = 162 | issue = 5 | pages = 1949-56 | month = Nov | year = 2000 | doi = 10.1164/ajrccm.162.5.9906096 | PMID = 11069839 }}</ref>   heat shock protein,<ref name="Kakugawa-2005">{{Cite journal | last1 = Kakugawa | first1 = T. | last2 = Mukae | first2 = H. | last3 = Hayashi | first3 = T. |last4 = Ishii | first4 = H. | last5 = Nakayama | first5 = S. | last6 = Sakamoto | first6 = N. | last7 = Yoshioka | first7 = S. | last8 = Sugiyama | first8 = K. | last9 = Mine | first9 = M. | title = Expression of HSP47 in usual interstitial pneumonia and nonspecific interstitial pneumonia. | journal = Respir Res | volume = 6 | issue = | pages = 57 | month = | year = 2005 | doi = 10.1186/1465-9921-6-57 | PMID = 15955241 }}</ref>  surfactant protein C<ref name="Thomas-2002">{{Cite journal | last1 = Thomas | first1 = AQ. | last2 = Lane | first2 = K. | last3 = Phillips | first3 = J. | last4 = Prince | first4 = M. | last5 = Markin | first5 = C. | last6 = Speer | first6 = M. | last7 = Schwartz | first7 = DA. | last8 = Gaddipati | first8 = R. | last9 = Marney | first9 = A. | title = Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred. | journal = Am J Respir Crit Care Med | volume = 165 | issue = 9 | pages = 1322-8 | month = May | year = 2002 | doi = 10.1164/rccm.200112-123OC | PMID = 11991887 }}</ref><ref name="Brasch-2004">{{Cite journal | last1 = Brasch | first1 = F. | last2 = Griese | first2 = M. | last3 = Tredano | first3 = M. | last4 = Johnen | first4 = G. | last5 = Ochs | first5 = M. | last6 = Rieger | first6 = C. | last7 = Mulugeta | first7 = S. | last8 = Müller | first8 = KM. | last9 = Bahuau | first9 = M. | title = Interstitial lung disease in a baby with a de novo mutation in the SFTPC gene. | journal = Eur Respir J | volume = 24 | issue = 1 | pages = 30-9 | month = Jul | year = 2004 | doi = | PMID = 15293602 }}</ref><ref name="Nogee-2001">{{Cite journal | last1 = Nogee | first1 = LM. | last2 = Dunbar | first2 = AE. | last3 = Wert | first3 = SE. | last4 = Askin | first4 = F. | last5 = Hamvas | first5 = A. | last6 = Whitsett | first6 = JA.| title = A mutation in the surfactant protein C gene associated with familial interstitial lung disease. | journal = N Engl J Med | volume = 344 | issue = 8 | pages = 573-9 | month = Feb | year = 2001 | doi = 10.1056/NEJM200102223440805 | PMID = 11207353 }}</ref><ref name="Stevens-2005">{{Cite journal | last1 = Stevens | first1 = PA. | last2 = Pettenazzo | first2 = A. | last3 = Brasch | first3 = F. | last4 = Mulugeta | first4 = S. | last5 = Baritussio | first5 = A. | last6 = Ochs | first6 = M. | last7 = Morrison | first7 = L. | last8 = Russo | first8 = SJ. | last9 = Beers | first9 = MF. | title = Nonspecific interstitial pneumonia, alveolar proteinosis, and abnormal proprotein trafficking resulting from a spontaneous mutation in the surfactant protein C gene. | journal = Pediatr Res | volume = 57 | issue = 1 |pages = 89-98 | month = Jan | year = 2005 | doi = 10.1203/01.PDR.0000147567.02473.5A | PMID = 15557112 }}</ref><ref name="Chibbar-2004">{{Cite journal | last1 = Chibbar | first1 = R. | last2 = Shih | first2 = F. | last3 = Baga | first3 = M. | last4 = Torlakovic | first4 = E. | last5 = Ramlall | first5 = K. | last6 = Skomro | first6 = R. | last7 = Cockcroft | first7 = DW. | last8 = Lemire | first8 = EG. | title = Nonspecific interstitial pneumonia and usual interstitial pneumonia with mutation in surfactant protein C in familial pulmonary fibrosis. | journal = Mod Pathol | volume = 17 | issue = 8 | pages = 973-80 |month = Aug | year = 2004 | doi = 10.1038/modpathol.3800149 | PMID = 15133475 }}</ref>
:*The coagulation system<ref name="Eitzman-1996">{{Cite journal | last1 = Eitzman | first1 = DT. | last2 = McCoy | first2 = RD. | last3 = Zheng |first3 = X. | last4 = Fay | first4 = WP. | last5 = Shen | first5 = T. | last6 = Ginsburg | first6 = D. | last7 = Simon | first7 = RH. | title = Bleomycin-induced pulmonary fibrosis in transgenic mice that either lack or overexpress the murine plasminogen activator inhibitor-1 gene. | journal = J Clin Invest | volume = 97 | issue = 1 | pages = 232-7 | month = Jan | year = 1996 | doi = 10.1172/JCI118396 | PMID = 8550840 }}</ref><ref name="Kim-">{{Cite journal | last1 = Kim | first1 = KK. | last2 = Flaherty | first2 = KR. | last3 = Long | first3 = Q. | last4 = Hattori | first4 = N. | last5 = Sisson | first5 = TH. |last6 = Colby | first6 = TV. | last7 = Travis | first7 = WD. | last8 = Martinez | first8 = FJ. | last9 = Murray | first9 = S. | title = A plasminogen activator inhibitor-1 promoter polymorphism and idiopathic interstitial pneumonia. | journal = Mol Med | volume = 9 | issue = 1-2 | pages = 52-6 | month = | year = | doi = | PMID = 12765340 }}</ref>
:*Intercellular adhesion molecules-1,<ref name="Takehara-2001">{{Cite journal | last1 = Takehara | first1 = H. | last2 = Tada | first2 = S. | last3 = Kataoka | first3 = M. | last4 = Matsuo | first4 = K. | last5 = Ueno | first5 = Y. | last6 = Ozaki | first6 = S. | last7 = Miyake | first7 = T. | last8 = Fujimori |first8 = Y. | last9 = Yamadori | first9 = I. | title = Intercellular adhesion molecule-1 in patients with idiopathic interstitial pneumonia. | journal = Acta Med Okayama | volume = 55 | issue = 4 | pages = 205-11 | month = Aug | year = 2001 | doi = | PMID = 11512562 }}</ref>  IL-4, IL-13, IL-18<ref name="Jakubzick-2004">{{Cite journal | last1 = Jakubzick | first1 = C. | last2 = Choi | first2 = ES. | last3 = Kunkel | first3 = SL. |last4 = Evanoff | first4 = H. | last5 = Martinez | first5 = FJ. | last6 = Puri | first6 = RK. | last7 = Flaherty | first7 = KR. | last8 = Toews | first8 = GB. | last9 = Colby | first9 = TV. | title = Augmented pulmonary IL-4 and IL-13 receptor subunit expression in idiopathic interstitial pneumonia. | journal = J Clin Pathol | volume = 57 | issue = 5 | pages = 477-86 | month = May | year = 2004 | doi = | PMID = 15113854 }}</ref>
:*Interferon-gamma
:*Pro fibrotic chemokines<ref name="Choi-2004">{{Cite journal | last1 = Choi | first1 = ES.| last2 = Jakubzick | first2 = C. | last3 = Carpenter | first3 = KJ. | last4 = Kunkel | first4 = SL. | last5 = Evanoff | first5 = H. | last6 = Martinez | first6 = FJ. | last7 = Flaherty | first7 = KR. | last8 = Toews | first8 = GB. | last9 = Colby | first9 = TV. | title = Enhanced monocyte chemoattractant protein-3/CC chemokine ligand-7 in usual interstitial pneumonia. | journal = Am J Respir Crit Care Med | volume = 170 | issue = 5 | pages = 508-15 | month = Sep | year = 2004 | doi = 10.1164/rccm.200401-002OC | PMID = 15191918 }}</ref>


===Desquamative Interstitial pneumonia (DIP)===
:*CCL7, and CCL5 
:*Lymphocytes<ref name="Keogh-2005">{{Cite journal | last1 = Keogh | first1 = KA. | last2 = Limper | first2 = AH. | title = Characterization of lymphocyte populations in nonspecific interstitial pneumonia.| journal = Respir Res | volume = 6 | issue = | pages = 137 | month = | year = 2005 | doi = 10.1186/1465-9921-6-137 | PMID = 16287509 }}</ref>
:*Dendritic cells
:*Fibroblasts


DIP lacks the patchy appearance that UIP normally presents with .In DIP alveolar walls are lined with chronic inflammatory cells and dense connective tissue and alveolar spaces are filled with macrophages. In desquamative interstitial pneumonia mild fibrosis without honeycomb changes are seen. Key changes are visualization of mononuclear changes at the distal spaces. These mononuclear cells appear as finely granular brown pigment with mottled tiny black particles. These may be called as smoker’s macrophage, which are different than desquamated pneumocytes. Some common overlapping changes between DIP and respiratory bronchiolitis are seen.<ref name="Moon-1999">{{Cite journal | last1 = Moon | first1 = J. | last2 = du Bois | first2 = RM. | last3 = Colby | first3 = TV. | last4 = Hansell | first4 = DM. | last5 = Nicholson | first5 = AG. | title = Clinical significance of respiratory bronchiolitis on open lung biopsy and its relationship to smoking related interstitial lung disease. | journal = Thorax | volume = 54 | issue = 11 | pages = 1009-14 | month = Nov | year = 1999 | doi = | PMID = 10525560 }}</ref><ref name="Yousem-1989">{{Cite journal | last1 = Yousem | first1 = SA. | last2 = Colby | first2 = TV. | last3 = Gaensler | first3 = EA. | title = Respiratory bronchiolitis-associated interstitial lung disease and its relationship to desquamative interstitial pneumonia. | journal = Mayo Clin Proc | volume = 64 | issue = 11 | pages = 1373-80 | month = Nov | year = 1989 | doi = | PMID = 2593722 }}</ref>
Some common associations between Idiopathic Non-specific Interstitial Pneumonia (NSIP) and Usual Interstitial Pneumonia (UIP) have been noted. Histologically patients can manifest lesions of both UIP and NSIP simultaneously.  The reason for this presentation is still unknown but environmental exposures and genetic mutations could be some of the causes.<ref name="Monaghan-2004">{{Cite journal | last1 = Monaghan | first1 = H. | last2 = Wells | first2 = AU. | last3 = Colby | first3 = TV. | last4 = du Bois | first4 = RM. | last5 = Hansell | first5 = DM. | last6 = Nicholson | first6 = AG. |title = Prognostic implications of histologic patterns in multiple surgical lung biopsies from patients with idiopathic interstitial pneumonias. | journal = Chest | volume = 125 | issue = 2 | pages = 522-6 |month = Feb | year = 2004 | doi = | PMID = 14769733 }}</ref><ref name="Flaherty-2001">{{Cite journal | last1 = Flaherty | first1 = KR. | last2 = Travis | first2 = WD. | last3 = Colby | first3 = TV. | last4 = Toews | first4 = GB. | last5 = Kazerooni | first5 = EA. | last6 = Gross | first6 = BH. | last7 = Jain | first7 = A. | last8 = Strawderman | first8 = RL. | last9 = Flint | first9 = A. | title = Histopathologic variability in usual and nonspecific interstitial pneumonias. | journal = Am J Respir Crit Care Med | volume = 164 | issue = 9 | pages = 1722-7 | month = Nov | year = 2001 | doi = 10.1164/ajrccm.164.9.2103074| PMID = 11719316 }}</ref>


Features differentiating NSIP and UIP include:


===Cryptogenic-Organizing pneumonia===
:* Irregular [[fibrosis]]
:* Honeycombing
:* Fibroblast predominant foci
:* Fibroblasts secreting transforming growth factor–Beta (TGF-β) and fibronectin<ref name="Miki-2000">{{Cite journal | last1 = Miki | first1 = H. | last2 = Mio | first2 = T. | last3 = Nagai | first3 = S. | last4 = Hoshino | first4 = Y. | last5 = Nagao | first5 = T. | last6 = Kitaichi | first6 = M. | last7 = Izumi | first7 = T. | title = Fibroblast contractility: usual interstitial pneumonia and nonspecific interstitial pneumonia. | journal = Am J Respir Crit Care Med | volume = 162 | issue = 6 | pages = 2259-64 | month = Dec | year = 2000 | doi = 10.1164/ajrccm.162.6.9812029 | PMID = 11112149 }}</ref>


Cryptogenic organizing pneumonia lesions consist more of fibroblasts and myofibroblasts in the alveolar ducts and alveoli. There might be involvement of polyps in the bronchial lumen in some patients. There is excess of granulation tissue deposition and sometimes this pattern of extension may appear like a butterfly.
===Respiratory Bronchiolitis-Interstitial Lung Disease ===
Dysorganization of the alveolar epithelium is what causes cryptogenic organizing pneumonia. This disorganization leads to plasma protein leakage, fibroblast migration and fibrin deposition inside the lumen. Involvement of the vascular endothelial growth factors and matrix metalloproteinase also adds up to the cause.<ref name="Qiu-2013">{{Cite journal | last1 = Qiu | first1 = YY. | last2 = Miao | first2 = LY. | last3 = Cai | first3 = HR. | last4 = Xiao | first4 = YL. | last5 = Ye | first5 = Q. | last6 = Meng | first6 = FQ. | last7 = Feng | first7 = AN. | title = [The clinicopathological features of acute fibrinous and organizing pneumonia]. | journal = Zhonghua Jie He He Hu Xi Za Zhi | volume = 36 | issue = 6 | pages = 425-30 | month = Jun | year = 2013 | doi = | PMID = 24103205 }}</ref>
*[[Cigarette smoking]] could be one of the major causative agent of Respiratory Bronchiolitis-Interstitial Lung Disease (RB-ILD). A relation between the duration and the intensity of cigarette smoking and visualization of opacities on chest radiographs was reported in a few studies.<ref name="Carilli-1973">{{Cite journal | last1 = Carilli | first1 = AD. | last2 = Kotzen | first2 = LM. | last3 = Fischer | first3 = MJ. | title = The chest roentgenogram in smoking females. | journal = Am Rev Respir Dis | volume = 107 | issue = 1 | pages = 133-6 | month = Jan | year = 1973 | doi = | PMID = 4683317 }}</ref><ref name="Weiss-1984">{{Cite journal | last1 = Weiss | first1 = W. | title = Cigarette smoke, asbestos, and small irregular opacities. | journal = Am Rev Respir Dis | volume = 130 | issue = 2 | pages = 293-301 | month = Aug | year = 1984 | doi = | PMID = 6380358 }}</ref><ref name="Weiss-1991">{{Cite journal | last1 = Weiss | first1 = W. | title = Cigarette smoking and small irregular opacities. | journal = Br J Ind Med | volume = 48 | issue = 12 | pages = 841-4 | month = Dec | year = 1991 | doi = | PMID = 1772799 }}</ref><ref name="Dick-1992">{{Cite journal | last1 = Dick | first1 = JA. | last2 = Morgan | first2 = WK. | last3 = Muir | first3 = DF. | last4 = Reger | first4 = RB. | last5 = Sargent | first5 = N. | title = The significance of irregular opacities on the chest roentgenogram. | journal = Chest | volume = 102 | issue = 1 | pages = 251-60 | month = Jul | year = 1992 | doi = | PMID = 1623762 }}</ref>
Some recent studies also show that it is a rare extra-intestinal manifestation of [[Crohn's Disease]].<ref name="Dinneen-2013">{{Cite journal | last1 = Dinneen | first1 = HS. | last2 = Samiullah | first2 = S. | last3 = Lenza | first3 = C. | title = Cryptogenic organizing pneumonia: A rare extra-intestinal manifestation of Crohn's disease. | journal = J Crohns Colitis | volume = | issue = | pages = | month = Oct | year = 2013 | doi = 10.1016/j.crohns.2013.09.006 | PMID = 24090908 }}</ref>
* The pathology is seen in the lumen of the bronchiole.  Sometimes the bronchioles, alveolar ducts and the peribronchiolar alveolar spaces may show clusters of dusty brown macrophages.<ref name="Myers-1987">{{Cite journal | last1 = Myers | first1 = JL. | last2 = Veal | first2 = CF. | last3 = Shin | first3 = MS. | last4 = Katzenstein | first4 = AL. | title = Respiratory bronchiolitis causing interstitial lung disease. A clinicopathologic study of six cases. | journal = Am Rev Respir Dis | volume = 135 | issue = 4 | pages = 880-4 | month = Apr | year = 1987 | doi = | PMID = 3565934 }}</ref><ref name="Yousem-1989">{{Cite journal | last1 = Yousem | first1 = SA. | last2 = Colby | first2 = TV. | last3 = Gaensler | first3 = EA. | title = Respiratory bronchiolitis-associated interstitial lung disease and its relationship to desquamative interstitial pneumonia. | journal = Mayo Clin Proc | volume = 64 | issue = 11 | pages = 1373-80 | month = Nov | year = 1989 | doi = | PMID = 2593722 }}</ref><ref name="Niewoehner-1974">{{Cite journal | last1 = Niewoehner | first1 = DE. | last2 = Kleinerman | first2 = J. | last3 = Rice | first3 = DB. | title = Pathologic changes in the peripheral airways of young cigarette smokers. | journal = N Engl J Med | volume = 291 | issue = 15 | pages = 755-8 | month = Oct | year = 1974 | doi = 10.1056/NEJM197410102911503 | PMID = 4414996 }}</ref><ref name="Churg-2010">{{Cite journal | last1 = Churg | first1 = A. | last2 = Müller | first2 = NL. | last3 = Wright | first3 = JL. | title = Respiratory bronchiolitis/interstitial lung disease: fibrosis, pulmonary function, and evolving concepts. | journal = Arch Pathol Lab Med | volume = 134 | issue = 1 | pages = 27-32 | month = Jan | year = 2010 | doi = 10.1043/1543-2165-134.1.27 | PMID = 20073602 }}</ref><ref name="Cosio-1980">{{Cite journal | last1 = Cosio | first1 = MG. | last2 = Hale | first2 = KA. | last3 = Niewoehner | first3 = DE. | title = Morphologic and morphometric effects of prolonged cigarette smoking on the small airways. | journal = Am Rev Respir Dis | volume = 122 | issue = 2 | pages = 265-21 | month = Aug | year = 1980 | doi = | PMID = 7416603 }}</ref><ref name="Colby-1998">{{Cite journal | last1 = Colby | first1 = TV. | title = Bronchiolitis. Pathologic considerations. | journal = Am J Clin Pathol | volume = 109 | issue = 1 | pages = 101-9 | month = Jan | year = 1998 | doi = | PMID = 9426525 }}</ref>
*Granular golden brown particles having plenty of cytoplasm may be seen.  These particles are PAS-positive and Prussian blue–positive which implies increased iron content in the alveolar macrophages.  This increased iron content could be associated with smoking.<ref name="Niewoehner-1974">{{Cite journal | last1 = Niewoehner | first1 = DE. | last2 = Kleinerman | first2 = J. | last3 = Rice | first3 = DB. | title = Pathologic changes in the peripheral airways of young cigarette smokers. | journal = N Engl J Med | volume = 291 | issue = 15 | pages = 755-8 | month = Oct | year = 1974 | doi = 10.1056/NEJM197410102911503 | PMID = 4414996 }}</ref><ref name="Cosio-1980">{{Cite journal | last1 = Cosio | first1 = MG. | last2 = Hale | first2 = KA. | last3 = Niewoehner | first3 = DE. | title = Morphologic and morphometric effects of prolonged cigarette smoking on the smallairways. | journal = Am Rev Respir Dis | volume = 122 | issue = 2 | pages = 265-21 | month = Aug | year = 1980 | doi = | PMID = 7416603 }}</ref><ref name="Churg-2010">{{Cite journal | last1 = Churg | first1 = A. | last2 = Müller | first2 = NL. | last3 = Wright | first3 = JL. | title = Respiratory bronchiolitis/interstitial lung disease: fibrosis, pulmonary function, and evolving concepts. | journal = Arch Pathol Lab Med | volume = 134 | issue = 1 | pages = 27-32 | month = Jan | year = 2010 | doi = 10.1043/1543-2165-134.1.27 | PMID = 20073602 }}</ref>
*A common feature of histology of DIP and respiratory bronchiolitis is a mixture of alveolar septal thickening, epithelial hyperplasia and pigmented macrophages in the lumen.  There are lymphocytes and histiocytes deposited in an irregular way in the submucosa.  Similar to the black pigment in the [[macrophages]], a dark black anthracotic pigment can be seen in the histiocytes.<ref name="Yousem-1989">{{Cite journal | last1 = Yousem | first1 = SA. | last2 = Colby | first2 = TV. | last3 = Gaensler | first3 = EA. | title = Respiratory bronchiolitis-associated interstitial lung disease and its relationship to desquamative interstitial pneumonia. | journal = Mayo Clin Proc | volume = 64 | issue = 11 | pages = 1373-80 | month = Nov | year = 1989 | doi = | PMID = 2593722 }}</ref><ref name="Colby-1998">{{Cite journal | last1 = Colby | first1 = TV. | title = Bronchiolitis. Pathologic considerations. | journal = Am J Clin Pathol | volume = 109 | issue = 1 | pages = 101-9 | month = Jan | year = 1998 | doi = | PMID = 9426525 }}</ref> Type 2 hyperplastic cells and cuboidal bronchiolar type epithelium line the fibrosis around the bronchioles.


===Desquamative Interstitial Pneumonia ===
* Desquamative interstitial pneumonia (DIP) lacks the typical patchy appearance of UIP.
* In DIP alveolar walls are lined with chronic inflammatory cells and dense connective tissue and the alveolar spaces are filled with macrophages.
* In DIP mild fibrosis without honeycomb changes are present occasionally.
* Eosinophilic and plasma cell infiltration are also seen.
* Mononuclear changes within the most distal spaces is a key finding in DIP.  These mononuclear cells appear as finely granular brown pigment with mottled tiny black particles.  These cells are known as smoker’s macrophages, which are different from the desquamated pneumocytes.
* Some of these changes overlap in both DIP and respiratory bronchiolitis.<ref name="Moon-1999">{{Cite journal | last1 = Moon | first1 = J. | last2 = du Bois | first2 = RM. | last3 = Colby | first3 = TV. | last4 = Hansell | first4 = DM. | last5 = Nicholson | first5 = AG. | title = Clinical significance of respiratory bronchiolitis on open lung biopsy and its relationship to smoking related interstitial lung disease. | journal = Thorax | volume = 54 | issue = 11 | pages = 1009-14 | month = Nov | year = 1999 | doi = | PMID = 10525560 }}</ref><ref name="Yousem-1989">{{Cite journal | last1 = Yousem | first1 = SA. | last2 = Colby | first2 = TV. | last3 = Gaensler | first3 = EA. | title = Respiratory bronchiolitis-associated interstitial lung disease and its relationship to desquamative interstitial pneumonia. | journal = Mayo Clin Proc | volume = 64 | issue = 11 | pages = 1373-80 | month = Nov | year = 1989 | doi = | PMID = 2593722 }}</ref>


===Acute Interstitial pneumonia (Hamman-Rich Syndrome) (AIP)===
===Cryptogenic-Organizing Pneumonia===
Cryptogenic organizing pneumonia (COP) is caused by disorganization of the alveolar epithelium.  COP is characterized by:
*Plasma protein leakage, fibroblast migration and fibrin deposition inside the lumen
*Involvement of the [[vascular endothelial growth factor]] and matrix metalloproteinases.<ref name="Qiu-2013">{{Cite journal | last1 = Qiu | first1 = YY. | last2 = Miao | first2 = LY. | last3 = Cai | first3 = HR. | last4 = Xiao | first4 = YL. | last5 = Ye | first5 = Q. | last6 = Meng | first6 = FQ. | last7 = Feng | first7 = AN. | title = [The clinicopathological features of acute fibrinous and organizing pneumonia]. | journal = Zhonghua Jie He He Hu Xi Za Zhi | volume = 36 | issue = 6 | pages = 425-30 | month = Jun | year = 2013 | doi = | PMID = 24103205 }}</ref>
*Accumulation of [[fibroblasts]] and [[myofibroblasts]] in the alveolar ducts and alveoli
*Involvement of polyps in the bronchial lumen in some patients
*Excess of granulation tissue deposition; the pattern of extension sometimes appearing like a butterfly


AIP has similar appearance as to diffuse alveolar damage (DAD). A majority of lung injury reacts via the same mechanism as diffuse interstitial pneumonia. It has three stages earlier exudative, then organized proliferative and last the chronic healed or fibrotic.<ref name="Olson-1990">{{Cite journal | last1 = Olson | first1 = J. | last2 = Colby | first2 = TV. | last3 = Elliott | first3 = CG. | title = Hamman-Rich syndrome revisited. | journal = Mayo Clin Proc | volume = 65 | issue = 12 | pages = 1538-48 | month = Dec | year = 1990 | doi = | PMID = 2255216 }}</ref><ref name="Katzenstein-1986">{{Cite journal | last1 = Katzenstein | first1 = AL. | last2 = Myers | first2 = JL. | last3 = Mazur | first3 = MT. | title = Acute interstitial pneumonia. A clinicopathologic, ultrastructural, and cell kinetic study. | journal = Am J Surg Pathol | volume = 10 | issue = 4 | pages = 256-67 | month = Apr | year = 1986 | doi = | PMID = 3706612 }}</ref>
Some recent studies show that COP can be a rare extra-intestinal manifestation of [[Crohn's Disease]].<ref name="Dinneen-2013">{{Cite journal | last1 = Dinneen | first1 = HS. | last2 = Samiullah | first2 = S. | last3 = Lenza | first3 = C. | title = Cryptogenic organizing pneumonia: A rare extra-intestinal manifestation of Crohn's disease. | journal = J Crohns Colitis | volume = | issue = | pages = | month = Oct | year = 2013 | doi = 10.1016/j.crohns.2013.09.006 | PMID = 24090908 }}</ref>
* Exudative stage: Histology specimen never obtained since patient presents late and biopsy are never obtained.
* Proliferative stage: Most typical change seen. A lot of inflammatory infiltration seen in the septa with destruction and hyaline membrane formation leading to thickening of the septa and interstitium.
* Chronic or healed phase: Diffuse scarring seen. A major differentiating factor between AIP and UIP in this phase is that AIP has similar type of lesion at one point of time whereas UIP has lesions of different ages and no specific one pattern could be found out at a period of time.


Release of [[tumor necrosis factor alpha]], interleukin 1β, monocyte chemoattractant factor and neutrophils cause further damage and release of toxic oxygen radicals and proteases. These causes exudate and cellular damage. A fibroblast proliferation and differentiation into myofibroblasts leads to collagen formation and widening of the septa. Later Hyaline membrane decrease in number and there is a rise in the number of type II epithelial cells. A few patients resolve after this stage whereas a majority progress to the next stage.
===Acute Interstitial pneumonia (Hamman-Rich Syndrome) ===
AIP shows  prominent myofibroblastic proliferation whereas this finding is only seen in a few cases of [[ARDS]] due to infection or drug toxicity .<ref name="Kang-2009">{{Cite journal | last1 = Kang | first1 = D. | last2 = Nakayama | first2 = T. | last3 = Togashi | first3 = M. | last4 = Yamamoto | first4 = M. | last5 = Takahashi | first5 = M. | last6 = Kunugi | first6 = S. | last7 = Ishizaki | first7 = M. | last8 = Fukuda | first8 = Y. | title = Two forms of diffuse alveolar damage in the lungs of patients with acute respiratory distress syndrome. | journal = Hum Pathol | volume = 40 | issue = 11 | pages = 1618-27 | month = Nov | year = 2009 | doi = 10.1016/j.humpath.2009.04.019 | PMID = 19647854 }}</ref><ref name="Pache-1998">{{Cite journal | last1 = Pache | first1 = JC. | last2 = Christakos | first2 = PG. | last3 = Gannon | first3 = DE. | last4 = Mitchell | first4 = JJ. | last5 = Low | first5 = RB. | last6 = Leslie | first6 = KO. | title = Myofibroblasts in diffuse alveolar damage of the lung. | journal = Mod Pathol | volume = 11 | issue = 11 | pages = 1064-70 | month = Nov | year = 1998 | doi = | PMID = 9831203 }}</ref>
Acute Interstitial Pneumonia (AIP) has a similar appearance to Diffuse Alveolar Damage (DAD). Shown below is a table summarizing the pathological features of the three different stages of AIP. It should be noted that similar lesions belonging to the same stage are seen in AIP whereas lesions of different ages are noted in UIP in the absence of a specific unified pattern at a given point of time. <ref name="Olson-1990">{{Cite journal | last1 = Olson | first1 = J. | last2 = Colby | first2 = TV. | last3 = Elliott | first3 = CG. | title = Hamman-Rich syndrome revisited. | journal = Mayo Clin Proc | volume = 65 | issue = 12 | pages = 1538-48 | month = Dec | year = 1990 | doi = | PMID = 2255216 }}</ref><ref name="Katzenstein-1986">{{Cite journal | last1 = Katzenstein | first1 = AL. | last2 = Myers | first2 = JL. | last3 = Mazur | first3 = MT. | title = Acute interstitial pneumonia. A clinicopathologic, ultrastructural, and cell kinetic study. | journal = Am J Surg Pathol | volume = 10 | issue = 4 | pages = 256-67 | month = Apr | year = 1986 | doi = | PMID = 3706612 }}</ref>


===Lymphoid Interstitial Pneumonia (LIP)===
{| {{table}}
| align="center" style="background:#f0f0f0" | '''Stage'''
| align="center" style="background:#f0f0f0 " | '''Pathological Feature '''
|-
|  Exudative stage|| Histology specimen is never obtained since patient presents late.
|-
| Proliferative stage|| Most commonly seen stage.<br> Inflammatory infiltration causes septal destruction and hyaline membrane formation leading to thickening of the septa and the interstitium.
|-
| Chronic or healed phase||Diffuse scarring is seen.
|-
|}


Characteristic findings are lymphoid and chronic cell infiltration predominantly in seen in the alveolar septa but sometimes may appear along bronchi and vessels. Granulomas specially non –caseating, fibrotic changes, honeycombing and loss of normal lung tissue could be seen as the disease progresses.<ref name="-2002">{{Cite journal | title = American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors, June 2001 and by the ERS Executive Committee, June 2001. | journal = Am J Respir Crit Care Med | volume = 165 | issue = 2 | pages = 277-304 | month = Jan | year = 2002 | doi = 10.1164/ajrccm.165.2.ats01 | PMID = 11790668 }}</ref><ref name="Koss-1987">{{Cite journal | last1 = Koss | first1 = MN. | last2 = Hochholzer | first2 = L. | last3 = Langloss | first3 = JM. | last4 = Wehunt | first4 = WD. | last5 = Lazarus | first5 = AA. | title = Lymphoid interstitial pneumonia: clinicopathological and immunopathological findings in 18 cases. | journal = Pathology | volume = 19 | issue = 2 | pages = 178-85 | month = Apr | year = 1987 | doi = | PMID = 3453998 }}</ref>.In LIP B cell polyclonality is seen which differentiates it from pulmonary lymphoma. In HIV T cell are more predominant. Some times no specific cell type are seen though.<ref name="Koss-1987">{{Cite journal | last1 = Koss | first1 = MN. | last2 = Hochholzer | first2 = L. | last3 = Langloss | first3 = JM. | last4 = Wehunt | first4 = WD. | last5 = Lazarus | first5 = AA. | title = Lymphoid interstitial pneumonia: clinicopathological and immunopathological findings in 18 cases. | journal = Pathology | volume = 19 | issue = 2 | pages = 178-85 | month = Apr | year = 1987 | doi = | PMID = 3453998 }}</ref><ref name="Travis-1992">{{Cite journal | last1 = Travis | first1 = WD. | last2 = Fox | first2 = CH. | last3 = Devaney | first3 = KO. | last4 = Weiss | first4 = LM. | last5 = O'Leary | first5 = TJ. | last6 = Ognibene | first6 = FP. | last7 = Suffredini | first7 = AF. | last8 = Rosen | first8 = MJ. | last9 = Cohen | first9 = MB. | title = Lymphoid pneumonitis in 50 adult patients infected with the human immunodeficiency virus: lymphocytic interstitial pneumonitis versus nonspecific interstitial pneumonitis. | journal = Hum Pathol | volume = 23 | issue = 5 | pages = 529-41 | month = May | year = 1992 | doi = | PMID = 1314778 }}</ref><ref name="Lin-1988">{{Cite journal | last1 = Lin | first1 = RY. | last2 = Gruber | first2 = PJ. | last3 = Saunders | first3 = R. | last4 = Perla | first4 = EN. | title = Lymphocytic interstitial pneumonitis in adult HIV infection. | journal = N Y State J Med | volume = 88 | issue = 5 | pages = 273-6 | month = May | year = 1988 | doi = | PMID = 3288914 }}</ref> A Bcl-6 gene mutation is somewhat believed to be associated with mucosa-associated lymphoid tissue (MALT), HIV and EBV and other virus negative LIP <ref name="Kurosu-2004">{{Cite journal | last1 = Kurosu | first1 = K. | last2 = Weiden | first2 = MD. | last3 = Takiguchi | first3 = Y. | last4 = Rom | first4 = WN. | last5 = Yumoto | first5 = N. | last6 = Jaishree | first6 = J. | last7 = Nakata | first7 = K. | last8 = Kasahara | first8 = Y. | last9 = Tanabe | first9 = N. | title = BCL-6 mutations in pulmonary lymphoproliferative disorders: demonstration of an aberrant immunological reaction in HIV-related lymphoid interstitial pneumonia. | journal = J Immunol | volume = 172 | issue = 11 | pages = 7116-22 | month = Jun | year = 2004 | doi = | PMID = 15153535 }}</ref>. Features like monoclonality, hilar involvement, pleural involvement, bronchial wall involvement all point towards a malignant transformation. <ref name="Turner-1984">{{Cite journal | last1 = Turner | first1 = RR. | last2 = Colby | first2 = TV. | last3 = Doggett | first3 = RS. | title = Well-differentiated lymphocytic lymphoma. A study of 47 patients with primary manifestation in the lung. | journal = Cancer | volume = 54 | issue = 10 | pages = 2088-96 | month = Nov | year = 1984 | doi = | PMID = 6386139 }}</ref>
*Release of [[tumor necrosis factor alpha]], interleukin 1β, monocyte chemoattractant factor and neutrophils cause further damage.  This damage in turn causes release of toxic oxygen radicals and proteases. Overall it leads to an exudate formation and cellular damage.
*A fibroblast proliferation and differentiation into myofibroblasts leads to collagen formation which widens the septa. Later hyaline membrane decreases and there is a rise in  the number of type II epithelial cells.
* A few patients resolve after this stage whereas a majority progress to the next stage i.e fibrosis.
AIP shows  prominent myofibroblastic proliferation whereas this finding is only seen in a few cases of [[ARDS]] secondary to infection or drug toxicity.<ref name="Kang-2009">{{Cite journal | last1 = Kang | first1 = D. | last2 = Nakayama | first2 = T. | last3 = Togashi | first3 = M. | last4 = Yamamoto | first4 = M. | last5 = Takahashi | first5 = M. | last6 = Kunugi | first6 = S. | last7 = Ishizaki | first7 = M. | last8 = Fukuda | first8 = Y. | title = Two forms of diffuse alveolar damage in the lungs of patients with acute respiratory distress syndrome. | journal = Hum Pathol | volume = 40 | issue = 11 | pages = 1618-27 | month = Nov | year = 2009 | doi = 10.1016/j.humpath.2009.04.019 | PMID = 19647854 }}</ref><ref name="Pache-1998">{{Cite journal | last1 = Pache | first1 = JC. | last2 = Christakos | first2 = PG. | last3 = Gannon | first3 = DE. | last4 = Mitchell | first4 = JJ. | last5 = Low | first5 = RB. | last6 = Leslie | first6 = KO. | title = Myofibroblasts in diffuse alveolar damage of the lung. | journal = Mod Pathol | volume = 11 | issue = 11 | pages = 1064-70 | month = Nov | year = 1998 | doi = | PMID = 9831203 }}</ref>


Shown below is an image depicting AIP:
[[File:800px-Acute interstitial pneumonia (AIP) Idiopathic DAD 3.jpg|400px|Acute Interstitial Pneumonia]]
===Lymphoid Interstitial Pneumonia ===
*Characteristic findings of Lymphoid Interstitial Pneumonia (LIP) are lymphoid and chronic cell infiltration predominantly seen in the alveolar septa but sometimes also seen around bronchi and vessels.
*[[Granulomas]] specially non–caseating, fibrotic changes, honeycombing and loss of normal lung tissue is also seen as the disease progresses.<ref name="-2002">{{Cite journal | title = American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors, June 2001 and by the ERS Executive Committee, June 2001. | journal = Am J Respir Crit Care Med | volume = 165 | issue = 2 | pages = 277-304 | month = Jan | year = 2002 | doi = 10.1164/ajrccm.165.2.ats01 | PMID = 11790668 }}</ref><ref name="Koss-1987">{{Cite journal | last1 = Koss | first1 = MN. | last2 = Hochholzer | first2 = L. | last3 = Langloss | first3 = JM. | last4 = Wehunt | first4 = WD. | last5 = Lazarus | first5 = AA. | title = Lymphoid interstitial pneumonia: clinicopathological and immunopathological findings in 18 cases. | journal = Pathology | volume = 19 | issue = 2 | pages = 178-85 | month = Apr | year = 1987 | doi = | PMID = 3453998 }}</ref>
*In LIP, B cell polyclonality differentiates it from pulmonary lymphoma whereas in HIV, T cells are more predominant. However, sometimes no specific cell types are seen.<ref name="Koss-1987">{{Cite journal | last1 = Koss | first1 = MN. | last2 = Hochholzer | first2 = L. | last3 = Langloss | first3 = JM. | last4 = Wehunt | first4 = WD. | last5 = Lazarus | first5 = AA. | title = Lymphoid interstitial pneumonia: clinicopathological and immunopathological findings in 18 cases. | journal = Pathology | volume = 19 | issue = 2 | pages = 178-85 | month = Apr | year = 1987 | doi = | PMID = 3453998 }}</ref><ref name="Travis-1992">{{Cite journal | last1 = Travis | first1 = WD. | last2 = Fox | first2 = CH. | last3 = Devaney | first3 = KO. | last4 = Weiss | first4 = LM. | last5 = O'Leary | first5 = TJ. | last6 = Ognibene | first6 = FP. | last7 = Suffredini | first7 = AF. | last8 = Rosen | first8 = MJ. | last9 = Cohen | first9 = MB. | title = Lymphoid pneumonitis in 50 adult patients infected with the human immunodeficiency virus: lymphocytic interstitial pneumonitis versus nonspecific interstitial pneumonitis. | journal = Hum Pathol | volume = 23 | issue = 5 | pages = 529-41 | month = May | year = 1992 | doi = | PMID = 1314778 }}</ref><ref name="Lin-1988">{{Cite journal | last1 = Lin | first1 = RY. | last2 = Gruber | first2 = PJ. | last3 = Saunders | first3 = R. | last4 = Perla | first4 = EN. | title = Lymphocytic interstitial pneumonitis in adult HIV infection. | journal = N Y State J Med | volume = 88 | issue = 5 | pages = 273-6 | month = May | year = 1988 | doi = | PMID = 3288914 }}</ref>
*A Bcl-6 gene mutation has been associated with mucosa-associated lymphoid tissue (MALT), [[HIV]] and [[EBV]] and other virus negative LIP.<ref name="Kurosu-2004">{{Cite journal | last1 = Kurosu | first1 = K. | last2 = Weiden | first2 = MD. | last3 = Takiguchi | first3 = Y. | last4 = Rom | first4 = WN. | last5 = Yumoto | first5 = N. | last6 = Jaishree | first6 = J. | last7 = Nakata | first7 = K. | last8 = Kasahara | first8 = Y. | last9 = Tanabe | first9 = N. | title = BCL-6 mutations in pulmonary lymphoproliferative disorders: demonstration of an aberrant immunological reaction in HIV-related lymphoid interstitial pneumonia. | journal = J Immunol | volume = 172 | issue = 11 | pages = 7116-22 | month = Jun | year = 2004 | doi = | PMID = 15153535 }}</ref>
*Features like monoclonality, hilar involvement, pleural involvement, bronchial wall involvement all point towards a malignant transformation.<ref name="Turner-1984">{{Cite journal | last1 = Turner | first1 = RR. | last2 = Colby | first2 = TV. | last3 = Doggett | first3 = RS. | title = Well-differentiated lymphocytic lymphoma. A study of 47 patients with primary manifestation in the lung. | journal = Cancer | volume = 54 | issue = 10 | pages = 2088-96 | month = Nov | year = 1984 | doi = | PMID = 6386139 }}</ref>


==References==
==References==
{{Reflist|2}}
{{Reflist|2}}
[[Category:Disease]]
[[Category:Pulmonology]]


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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Chetan Lokhande, M.B.B.S [2]

Overview

Idiopathic interstitial pneumonia (IIP) is a disease entity that can be histologically classified into different categories. Idiopathic pulmonary fibrosis has the same features as that of usual interstitial pneumonia (UIP) whereas no specific pattern or common feature is noted among the other types of IIP. The pathophysiology of IIP can be summarized in the following three stages: recruitment of inflammatory cells, abnormal collagen deposition and fibroblastic proliferation and lastly progression to fibrosis.

Pathophysiology

Idiopathic Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) has often been considered an autoimmune disease. However, it is perhaps better characterized as an abnormal and excessive deposition of fibrotic tissue in the pulmonary interstitium with minimal associated inflammation.[1] Autoantibodies, a hallmark of autoimmune diseases, are found in a minority of patients with true idiopathic pulmonary fibrosis. Moreover, many autoimmune diseases that are associated with pulmonary fibrosis such as scleroderma, are more frequently associated with a related but more inflammatory disease, nonspecific interstitial pneumonitis.[2] IPF is associated with smoking[3] and exhibits some dependency on the amount of smoking.[4]


Shown below is an image depicting IPF:

Idiopathic Pulmonary Fibrosis

Idiopathic Non-specific Interstitial Pneumonia

As the name implies, idiopathic non-specific interstitial pneumonia (NSIP) has very inconsistent and non-specific findings.[5][6][7] Changes similar to other cases of interstitial pneumonia are seen which are migration of inflammatory cells in the alveolar septa and its widening with or without fibrosis. NSIP can be divided into three groups based on histopathological changes.[8] Shown below is a table summarizing the pathological findings in the three groups of NSIP:

Stage Pathological Feature
Group I Inflammatory cells predominant stage
Group II Accompanying fibrosis
Group III Fibrosis prevalent

Bronchoalveloar lavage (BAL) reveals the presence of lymphocytes in the alveolar septum which is an evidence of the involvement of the immune system.[6][9][10][11] A greater number of dendritic cells (DC), which help in antigen presentation, are visualized in close association with CD4 and CD8 lymphocytes in the biopsy of NSIS patients than in UIP.[12] Fibroblasts are the key cells involved in fibrotic lung diseases.[13]

The pathological mechanism of NSIP involves:

  • CCL7, and CCL5
  • Lymphocytes[28]
  • Dendritic cells
  • Fibroblasts

Some common associations between Idiopathic Non-specific Interstitial Pneumonia (NSIP) and Usual Interstitial Pneumonia (UIP) have been noted. Histologically patients can manifest lesions of both UIP and NSIP simultaneously. The reason for this presentation is still unknown but environmental exposures and genetic mutations could be some of the causes.[29][5]

Features differentiating NSIP and UIP include:

  • Irregular fibrosis
  • Honeycombing
  • Fibroblast predominant foci
  • Fibroblasts secreting transforming growth factor–Beta (TGF-β) and fibronectin[30]

Respiratory Bronchiolitis-Interstitial Lung Disease

  • Cigarette smoking could be one of the major causative agent of Respiratory Bronchiolitis-Interstitial Lung Disease (RB-ILD). A relation between the duration and the intensity of cigarette smoking and visualization of opacities on chest radiographs was reported in a few studies.[31][32][33][34]
  • The pathology is seen in the lumen of the bronchiole. Sometimes the bronchioles, alveolar ducts and the peribronchiolar alveolar spaces may show clusters of dusty brown macrophages.[35][36][37][38][39][40]
  • Granular golden brown particles having plenty of cytoplasm may be seen. These particles are PAS-positive and Prussian blue–positive which implies increased iron content in the alveolar macrophages. This increased iron content could be associated with smoking.[37][39][38]
  • A common feature of histology of DIP and respiratory bronchiolitis is a mixture of alveolar septal thickening, epithelial hyperplasia and pigmented macrophages in the lumen. There are lymphocytes and histiocytes deposited in an irregular way in the submucosa. Similar to the black pigment in the macrophages, a dark black anthracotic pigment can be seen in the histiocytes.[36][40] Type 2 hyperplastic cells and cuboidal bronchiolar type epithelium line the fibrosis around the bronchioles.

Desquamative Interstitial Pneumonia

  • Desquamative interstitial pneumonia (DIP) lacks the typical patchy appearance of UIP.
  • In DIP alveolar walls are lined with chronic inflammatory cells and dense connective tissue and the alveolar spaces are filled with macrophages.
  • In DIP mild fibrosis without honeycomb changes are present occasionally.
  • Eosinophilic and plasma cell infiltration are also seen.
  • Mononuclear changes within the most distal spaces is a key finding in DIP. These mononuclear cells appear as finely granular brown pigment with mottled tiny black particles. These cells are known as smoker’s macrophages, which are different from the desquamated pneumocytes.
  • Some of these changes overlap in both DIP and respiratory bronchiolitis.[41][36]

Cryptogenic-Organizing Pneumonia

Cryptogenic organizing pneumonia (COP) is caused by disorganization of the alveolar epithelium. COP is characterized by:

  • Plasma protein leakage, fibroblast migration and fibrin deposition inside the lumen
  • Involvement of the vascular endothelial growth factor and matrix metalloproteinases.[42]
  • Accumulation of fibroblasts and myofibroblasts in the alveolar ducts and alveoli
  • Involvement of polyps in the bronchial lumen in some patients
  • Excess of granulation tissue deposition; the pattern of extension sometimes appearing like a butterfly

Some recent studies show that COP can be a rare extra-intestinal manifestation of Crohn's Disease.[43]

Acute Interstitial pneumonia (Hamman-Rich Syndrome)

Acute Interstitial Pneumonia (AIP) has a similar appearance to Diffuse Alveolar Damage (DAD). Shown below is a table summarizing the pathological features of the three different stages of AIP. It should be noted that similar lesions belonging to the same stage are seen in AIP whereas lesions of different ages are noted in UIP in the absence of a specific unified pattern at a given point of time. [44][45]

Stage Pathological Feature
Exudative stage Histology specimen is never obtained since patient presents late.
Proliferative stage Most commonly seen stage.
Inflammatory infiltration causes septal destruction and hyaline membrane formation leading to thickening of the septa and the interstitium.
Chronic or healed phase Diffuse scarring is seen.
  • Release of tumor necrosis factor alpha, interleukin 1β, monocyte chemoattractant factor and neutrophils cause further damage. This damage in turn causes release of toxic oxygen radicals and proteases. Overall it leads to an exudate formation and cellular damage.
  • A fibroblast proliferation and differentiation into myofibroblasts leads to collagen formation which widens the septa. Later hyaline membrane decreases and there is a rise in the number of type II epithelial cells.
  • A few patients resolve after this stage whereas a majority progress to the next stage i.e fibrosis.

AIP shows prominent myofibroblastic proliferation whereas this finding is only seen in a few cases of ARDS secondary to infection or drug toxicity.[46][47]

Shown below is an image depicting AIP:

Acute Interstitial Pneumonia

Lymphoid Interstitial Pneumonia

  • Characteristic findings of Lymphoid Interstitial Pneumonia (LIP) are lymphoid and chronic cell infiltration predominantly seen in the alveolar septa but sometimes also seen around bronchi and vessels.
  • Granulomas specially non–caseating, fibrotic changes, honeycombing and loss of normal lung tissue is also seen as the disease progresses.[48][49]
  • In LIP, B cell polyclonality differentiates it from pulmonary lymphoma whereas in HIV, T cells are more predominant. However, sometimes no specific cell types are seen.[49][50][51]
  • A Bcl-6 gene mutation has been associated with mucosa-associated lymphoid tissue (MALT), HIV and EBV and other virus negative LIP.[52]
  • Features like monoclonality, hilar involvement, pleural involvement, bronchial wall involvement all point towards a malignant transformation.[53]

References

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  2. ↑ King, Jr., Talmadge E. (2005). "Centennial review: clinical advances in the diagnosis and therapy of the interstitial lung diseases". American Journal of Respiratory and Critical Care Medicine. 172 (3): 268–79.
  3. ↑ Nagai, Sonoko (2000). "Smoking-related interstitial lung diseases". Current Opinion in Pulmonary Medicine. 6 (5): 415–9. PMID 10958232. Unknown parameter |coauthors= ignored (help)
  4. ↑ Baumgartner, KB (1997). "Cigarette smoking: a risk factor for idiopathic pulmonary fibrosis". American Journal of Respiratory and Critical Care Medicine. 155 (1): 242–248. PMID 9001319. Unknown parameter |coauthors= ignored (help)
  5. ↑ 5.0 5.1 Flaherty, KR.; Travis, WD.; Colby, TV.; Toews, GB.; Kazerooni, EA.; Gross, BH.; Jain, A.; Strawderman, RL.; Flint, A. (2001). "Histopathologic variability in usual and nonspecific interstitial pneumonias". Am J Respir Crit Care Med. 164 (9): 1722–7. doi:10.1164/ajrccm.164.9.2103074. PMID 11719316. Unknown parameter |month= ignored (help)
  6. ↑ 6.0 6.1 Cottin, V.; Donsbeck, AV.; Revel, D.; Loire, R.; Cordier, JF. (1998). "Nonspecific interstitial pneumonia. Individualization of a clinicopathologic entity in a series of 12 patients". Am J Respir Crit Care Med. 158 (4): 1286–93. doi:10.1164/ajrccm.158.4.9802119. PMID 9769293. Unknown parameter |month= ignored (help)
  7. ↑ Katzenstein, AL.; Myers, JL. (2000). "Nonspecific interstitial pneumonia and the other idiopathic interstitial pneumonias: classification and diagnostic criteria". Am J Surg Pathol. 24 (1): 1–3. PMID 10632482. Unknown parameter |month= ignored (help)
  8. ↑ Katzenstein, AL.; Fiorelli, RF. (1994). "Nonspecific interstitial pneumonia/fibrosis. Histologic features and clinical significance". Am J Surg Pathol. 18 (2): 136–47. PMID 8291652. Unknown parameter |month= ignored (help)
  9. ↑ Fujita, J.; Yamadori, I.; Suemitsu, I.; Yoshinouchi, T.; Ohtsuki, Y.; Yamaji, Y.; Kamei, T.; Kobayashi, M.; Nakamura, Y. (1999). "Clinical features of non-specific interstitial pneumonia". Respir Med. 93 (2): 113–8. PMID 10464862. Unknown parameter |month= ignored (help)
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  19. ↑ Brasch, F.; Griese, M.; Tredano, M.; Johnen, G.; Ochs, M.; Rieger, C.; Mulugeta, S.; Müller, KM.; Bahuau, M. (2004). "Interstitial lung disease in a baby with a de novo mutation in the SFTPC gene". Eur Respir J. 24 (1): 30–9. PMID 15293602. Unknown parameter |month= ignored (help)
  20. ↑ Nogee, LM.; Dunbar, AE.; Wert, SE.; Askin, F.; Hamvas, A.; Whitsett, JA. (2001). "A mutation in the surfactant protein C gene associated with familial interstitial lung disease". N Engl J Med. 344 (8): 573–9. doi:10.1056/NEJM200102223440805. PMID 11207353. Unknown parameter |month= ignored (help)
  21. ↑ Stevens, PA.; Pettenazzo, A.; Brasch, F.; Mulugeta, S.; Baritussio, A.; Ochs, M.; Morrison, L.; Russo, SJ.; Beers, MF. (2005). "Nonspecific interstitial pneumonia, alveolar proteinosis, and abnormal proprotein trafficking resulting from a spontaneous mutation in the surfactant protein C gene". Pediatr Res. 57 (1): 89–98. doi:10.1203/01.PDR.0000147567.02473.5A. PMID 15557112. Unknown parameter |month= ignored (help)
  22. ↑ Chibbar, R.; Shih, F.; Baga, M.; Torlakovic, E.; Ramlall, K.; Skomro, R.; Cockcroft, DW.; Lemire, EG. (2004). "Nonspecific interstitial pneumonia and usual interstitial pneumonia with mutation in surfactant protein C in familial pulmonary fibrosis". Mod Pathol. 17 (8): 973–80. doi:10.1038/modpathol.3800149. PMID 15133475. Unknown parameter |month= ignored (help)
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  24. ↑ Kim, KK.; Flaherty, KR.; Long, Q.; Hattori, N.; Sisson, TH.; Colby, TV.; Travis, WD.; Martinez, FJ.; Murray, S. "A plasminogen activator inhibitor-1 promoter polymorphism and idiopathic interstitial pneumonia". Mol Med. 9 (1–2): 52–6. PMID 12765340.
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  26. ↑ Jakubzick, C.; Choi, ES.; Kunkel, SL.; Evanoff, H.; Martinez, FJ.; Puri, RK.; Flaherty, KR.; Toews, GB.; Colby, TV. (2004). "Augmented pulmonary IL-4 and IL-13 receptor subunit expression in idiopathic interstitial pneumonia". J Clin Pathol. 57 (5): 477–86. PMID 15113854. Unknown parameter |month= ignored (help)
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  41. ↑ Moon, J.; du Bois, RM.; Colby, TV.; Hansell, DM.; Nicholson, AG. (1999). "Clinical significance of respiratory bronchiolitis on open lung biopsy and its relationship to smoking related interstitial lung disease". Thorax. 54 (11): 1009–14. PMID 10525560. Unknown parameter |month= ignored (help)
  42. ↑ Qiu, YY.; Miao, LY.; Cai, HR.; Xiao, YL.; Ye, Q.; Meng, FQ.; Feng, AN. (2013). "[The clinicopathological features of acute fibrinous and organizing pneumonia]". Zhonghua Jie He He Hu Xi Za Zhi. 36 (6): 425–30. PMID 24103205. Unknown parameter |month= ignored (help)
  43. ↑ Dinneen, HS.; Samiullah, S.; Lenza, C. (2013). "Cryptogenic organizing pneumonia: A rare extra-intestinal manifestation of Crohn's disease". J Crohns Colitis. doi:10.1016/j.crohns.2013.09.006. PMID 24090908. Unknown parameter |month= ignored (help)
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  45. ↑ Katzenstein, AL.; Myers, JL.; Mazur, MT. (1986). "Acute interstitial pneumonia. A clinicopathologic, ultrastructural, and cell kinetic study". Am J Surg Pathol. 10 (4): 256–67. PMID 3706612. Unknown parameter |month= ignored (help)
  46. ↑ Kang, D.; Nakayama, T.; Togashi, M.; Yamamoto, M.; Takahashi, M.; Kunugi, S.; Ishizaki, M.; Fukuda, Y. (2009). "Two forms of diffuse alveolar damage in the lungs of patients with acute respiratory distress syndrome". Hum Pathol. 40 (11): 1618–27. doi:10.1016/j.humpath.2009.04.019. PMID 19647854. Unknown parameter |month= ignored (help)
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  48. ↑ "American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors, June 2001 and by the ERS Executive Committee, June 2001". Am J Respir Crit Care Med. 165 (2): 277–304. 2002. doi:10.1164/ajrccm.165.2.ats01. PMID 11790668. Unknown parameter |month= ignored (help)
  49. ↑ 49.0 49.1 Koss, MN.; Hochholzer, L.; Langloss, JM.; Wehunt, WD.; Lazarus, AA. (1987). "Lymphoid interstitial pneumonia: clinicopathological and immunopathological findings in 18 cases". Pathology. 19 (2): 178–85. PMID 3453998. Unknown parameter |month= ignored (help)
  50. ↑ Travis, WD.; Fox, CH.; Devaney, KO.; Weiss, LM.; O'Leary, TJ.; Ognibene, FP.; Suffredini, AF.; Rosen, MJ.; Cohen, MB. (1992). "Lymphoid pneumonitis in 50 adult patients infected with the human immunodeficiency virus: lymphocytic interstitial pneumonitis versus nonspecific interstitial pneumonitis". Hum Pathol. 23 (5): 529–41. PMID 1314778. Unknown parameter |month= ignored (help)
  51. ↑ Lin, RY.; Gruber, PJ.; Saunders, R.; Perla, EN. (1988). "Lymphocytic interstitial pneumonitis in adult HIV infection". N Y State J Med. 88 (5): 273–6. PMID 3288914. Unknown parameter |month= ignored (help)
  52. ↑ Kurosu, K.; Weiden, MD.; Takiguchi, Y.; Rom, WN.; Yumoto, N.; Jaishree, J.; Nakata, K.; Kasahara, Y.; Tanabe, N. (2004). "BCL-6 mutations in pulmonary lymphoproliferative disorders: demonstration of an aberrant immunological reaction in HIV-related lymphoid interstitial pneumonia". J Immunol. 172 (11): 7116–22. PMID 15153535. Unknown parameter |month= ignored (help)
  53. ↑ Turner, RR.; Colby, TV.; Doggett, RS. (1984). "Well-differentiated lymphocytic lymphoma. A study of 47 patients with primary manifestation in the lung". Cancer. 54 (10): 2088–96. PMID 6386139. Unknown parameter |month= ignored (help)

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