Hamman-Rich syndrome classification: Difference between revisions

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{{CMG}}; {{AE}} {{CK}}
{{CMG}}; {{AE}} {{CK}}
==Overview==
==Overview==
According to American Thoracic Society/European Respiratory Society (ATS/ERS) 2002 consensus, [[Hamman-Rich syndrome|Acute interstitial pneumonitis]] is a variant of a group of Idiopathic [[Interstitial lung disease|interstitial lung diseases]].
According to American Thoracic Society/European Respiratory Society (ATS/ERS) 2002 consensus, [[Hamman-Rich syndrome|Acute interstitial pneumonitis]] is an entity of a group of Idiopathic interstitial lung diseases. The classification is based on [[clinical]], [[Radiology|radiological]] and [[Histopathology|histopathologic]] findings. The [[classification]] has been updated by ATS/ERS International multidisciplinary panel recently based on the [[literature review]] on idiopathic interstitial lung diseases published between 2000-2011.
 
The classification is based on [[clinical]], [[Radiology|radiological]] and [[Histopathology|histopathologic]] findings.


==Classification==
==Classification==
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**[[Hamman-Rich syndrome|Acute interstitial pneumonia]]
**[[Hamman-Rich syndrome|Acute interstitial pneumonia]]
**[[Lymphocytic interstitial pneumonia]] (LIP)
**[[Lymphocytic interstitial pneumonia]] (LIP)
*American Thoracic Society/European Respiratory Society (ATS/ERS) panel classification of Idiopathic interstitial lung diseases has been updated recently during 2010-2011 reviewed changes to previously described clinical entities, describing new clinical entities, and describing new [[Histology|histologic patterns]].<ref name="pmid24032382">{{cite journal |vauthors=Travis WD, Costabel U, Hansell DM, King TE, Lynch DA, Nicholson AG, Ryerson CJ, Ryu JH, Selman M, Wells AU, Behr J, Bouros D, Brown KK, Colby TV, Collard HR, Cordeiro CR, Cottin V, Crestani B, Drent M, Dudden RF, Egan J, Flaherty K, Hogaboam C, Inoue Y, Johkoh T, Kim DS, Kitaichi M, Loyd J, Martinez FJ, Myers J, Protzko S, Raghu G, Richeldi L, Sverzellati N, Swigris J, Valeyre D |title=An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias |journal=Am. J. Respir. Crit. Care Med. |volume=188 |issue=6 |pages=733–48 |date=September 2013 |pmid=24032382 |pmc=5803655 |doi=10.1164/rccm.201308-1483ST |url=}}</ref>
*American Thoracic Society/European Respiratory Society (ATS/ERS) panel [[classification]] of Idiopathic [[Interstitial lung disease|interstitial lung diseases]] has been updated recently,including changes to previously described clinical entities, describing new clinical entities, and describing new [[Histology|histologic patterns]] using [[literature review]] between 2000-2011.<ref name="pmid24032382">{{cite journal |vauthors=Travis WD, Costabel U, Hansell DM, King TE, Lynch DA, Nicholson AG, Ryerson CJ, Ryu JH, Selman M, Wells AU, Behr J, Bouros D, Brown KK, Colby TV, Collard HR, Cordeiro CR, Cottin V, Crestani B, Drent M, Dudden RF, Egan J, Flaherty K, Hogaboam C, Inoue Y, Johkoh T, Kim DS, Kitaichi M, Loyd J, Martinez FJ, Myers J, Protzko S, Raghu G, Richeldi L, Sverzellati N, Swigris J, Valeyre D |title=An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias |journal=Am. J. Respir. Crit. Care Med. |volume=188 |issue=6 |pages=733–48 |date=September 2013 |pmid=24032382 |pmc=5803655 |doi=10.1164/rccm.201308-1483ST |url=}}</ref>
*Revised classification of American thoracic society/European respiratory society international multidisciplinary panel of [[Idiopathic interstitial pneumonia|Idiopathic interstitial pneumonias]]: 
**Major idiopathic interstitial pneumonias
**Major idiopathic interstitial pneumonias
***[[Idiopathic pulmonary fibrosis]]
***[[Idiopathic pulmonary fibrosis]]

Latest revision as of 20:56, 23 March 2018

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Chandrakala Yannam, MD [2]

Overview

According to American Thoracic Society/European Respiratory Society (ATS/ERS) 2002 consensus, Acute interstitial pneumonitis is an entity of a group of Idiopathic interstitial lung diseases. The classification is based on clinical, radiological and histopathologic findings. The classification has been updated by ATS/ERS International multidisciplinary panel recently based on the literature review on idiopathic interstitial lung diseases published between 2000-2011.

Classification


References

  1. "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. January 2002. doi:10.1164/ajrccm.165.2.ats01. PMID 11790668.
  2. Leslie KO (November 2005). "Historical perspective: a pathologic approach to the classification of idiopathic interstitial pneumonias". Chest. 128 (5 Suppl 1): 513S–519S. doi:10.1378/chest.128.5_suppl_1.513S. PMID 16304241.
  3. Travis WD, Costabel U, Hansell DM, King TE, Lynch DA, Nicholson AG, Ryerson CJ, Ryu JH, Selman M, Wells AU, Behr J, Bouros D, Brown KK, Colby TV, Collard HR, Cordeiro CR, Cottin V, Crestani B, Drent M, Dudden RF, Egan J, Flaherty K, Hogaboam C, Inoue Y, Johkoh T, Kim DS, Kitaichi M, Loyd J, Martinez FJ, Myers J, Protzko S, Raghu G, Richeldi L, Sverzellati N, Swigris J, Valeyre D (September 2013). "An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias". Am. J. Respir. Crit. Care Med. 188 (6): 733–48. doi:10.1164/rccm.201308-1483ST. PMC 5803655. PMID 24032382.

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