Granulomatosis with polyangiitis physical examination: Difference between revisions

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__NOTOC__
__NOTOC__
{{Wegener's granulomatosis}}
{{Wegener's granulomatosis}}
{{CMG}}{{APM}}{{AE}}{{KW}}
{{CMG}}{{APM}}{{AE}}{{ADS}}{{KW}}


==Overview==
==Overview==
A complete medical history and a comprehensive renal, pulmonary, and ENT examination must be preformed to help identify and properly diagnose Granulomatosis with polyangiitis from other diseases.
The important physical exam findings are [[Ulcerations]], palpable [[purpura]] and subcutaneous [[nodules]] in the skin; [[conjunctivitis]], [[uveitis]], [[sinusitis]], [[purulent]] exudate from nares,[[saddle nose]] deformity, reduced hearing in the head and neck; [[pleuritic chest pain]] ans signs of [[atelectasis]] in lung examination; and signs of [[mononeuritis multiplex]] on neural exam.


*
* Cranial nerve paralysis
==Physical Examination==
==Physical Examination==
*Physical examination of patients with Granulomatosis with polyangiitis  is usually remarkable for:<ref name="pmid15210387">{{cite journal |vauthors=Seo P, Stone JH |title=The antineutrophil cytoplasmic antibody-associated vasculitides |journal=Am. J. Med. |volume=117 |issue=1 |pages=39–50 |date=July 2004 |pmid=15210387 |doi=10.1016/j.amjmed.2004.02.030 |url=}}</ref><ref name="pmid17106496">{{cite journal |vauthors=Graves N |title=Wegener granulomatosis |journal=Proc (Bayl Univ Med Cent) |volume=19 |issue=4 |pages=342–4 |date=October 2006 |pmid=17106496 |pmc=1618758 |doi= |url=}}</ref>
*Physical examination of patients with Granulomatosis with polyangiitis  is usually remarkable for:<ref name="pmid15210387">{{cite journal |vauthors=Seo P, Stone JH |title=The antineutrophil cytoplasmic antibody-associated vasculitides |journal=Am. J. Med. |volume=117 |issue=1 |pages=39–50 |date=July 2004 |pmid=15210387 |doi=10.1016/j.amjmed.2004.02.030 |url=}}</ref><ref name="pmid17106496">{{cite journal |vauthors=Graves N |title=Wegener granulomatosis |journal=Proc (Bayl Univ Med Cent) |volume=19 |issue=4 |pages=342–4 |date=October 2006 |pmid=17106496 |pmc=1618758 |doi= |url=}}</ref>
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* [[Xanthelasma]]  
* [[Xanthelasma]]  
* [[Purulent]] exudate from the nares  
* [[Purulent]] exudate from the nares  
* [[Sinusitis]]  
* [[Sinusitis]]<ref name="pmid19263410">{{cite journal |vauthors=Cannady SB, Batra PS, Koening C, Lorenz RR, Citardi MJ, Langford C, Hoffman GS |title=Sinonasal Wegener granulomatosis: a single-institution experience with 120 cases |journal=Laryngoscope |volume=119 |issue=4 |pages=757–61 |date=April 2009 |pmid=19263410 |doi=10.1002/lary.20161 |url=}}</ref>
* [[Saddle nose]] deformity
* [[Saddle nose]] deformity
* [[Otitis Media]]  
* [[Otitis Media]]  
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===Neck===
===Neck===
* Neck examination of patients with granulomatosis with polyangiitis is usually normal
* Neck examination of patients with granulomatosis with polyangiitis is usually normal.
===Lungs===
===Lungs===
* Asymmetric chest expansion / Decreased chest expansion
Examination may show signs of:
*Lungs are hypo/hyperresonant
*[[Pleuritic pain]]
*Fine/coarse [[crackles]] upon auscultation of the lung bases/apices unilaterally/bilaterally
*[[Atelectasis physical examination|Atelectasis]]
*Rhonchi
* [[Pleural effusion physical examination|Pleural effusion]]
*Vesicular breath sounds / Distant breath sounds
* [[Pulmonary hypertension physical examination|Pulmonary hypertension]]- bibasilar crackles
*Expiratory/inspiratory wheezing with normal / delayed expiratory phase
* [[Subglottic stenosis]]
*[[Wheezing]] may be present
*[[Egophony]] present/absent
*[[Bronchophony]] present/absent
*Normal/reduced [[tactile fremitus]]
*Atelectasis
* Pleural effusion


===Heart===
===Heart===
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*[[Heart sounds#Second heart tone S2 the "dub"(components A2 and P2)|S2]]
*[[Heart sounds#Second heart tone S2 the "dub"(components A2 and P2)|S2]]
===Abdomen===
===Abdomen===
Abdominal examination of patients with [disease name] is usually normal.
*[[Abdominal tenderness]] may be present<ref name="pmid15758841">{{cite journal |vauthors=Pagnoux C, Mahr A, Cohen P, Guillevin L |title=Presentation and outcome of gastrointestinal involvement in systemic necrotizing vasculitides: analysis of 62 patients with polyarteritis nodosa, microscopic polyangiitis, Wegener granulomatosis, Churg-Strauss syndrome, or rheumatoid arthritis-associated vasculitis |journal=Medicine (Baltimore) |volume=84 |issue=2 |pages=115–28 |date=March 2005 |pmid=15758841 |doi= |url=}}</ref>
 
OR
*[[Abdominal distention]]
*[[Abdominal tenderness]] in the right/left upper/lower abdominal quadrant
*[[Rebound tenderness]] (positive Blumberg sign)
*A palpable abdominal mass in the right/left upper/lower abdominal quadrant
*Guarding may be present
*Guarding may be present
*[[Hepatomegaly]] / [[splenomegaly]] / [[hepatosplenomegaly]]
*Additional findings, such as obturator test, psoas test, McBurney point test, Murphy test


===Back===
===Back===
* Back examination of patients with [disease name] is usually normal.
* Back examination of patients with granulomatosis with polyangiitis is usually normal.
===Genitourinary===
===Genitourinary===
* Genitourinary examination of patients with [disease name] is usually normal.
OR
*A pelvic/adnexal mass may be palpated
*A pelvic/adnexal mass may be palpated
*Inflamed mucosa
*Inflamed mucosa
*Clear/(color), foul-smelling/odorless penile/vaginal discharge


===Neuromuscular===
===Neuromuscular===
*Patient is usually oriented to persons, place, and time
*Patient is usually oriented to persons, place, and time
*[[Mononeuritis multiplex]]- Loss of sensory and motor functions
*[[Mononeuritis multiplex]]<ref name="pmid28273992">{{cite journal |vauthors=Anadure R, Narayanan C, Varadraj G, Nandeesh B |title=ANCA Associated Mononeuritis Multiplex with Overlap in Vasculitic Syndromes |journal=J Clin Diagn Res |volume=11 |issue=1 |pages=OD01–OD03 |date=January 2017 |pmid=28273992 |pmc=5324437 |doi=10.7860/JCDR/2017/22252.9149 |url=}}</ref>- Loss of sensory and motor functions
*
*Cranial nerve paralysis
===Extremities===
===Extremities===
* Extremities examination of patients with [disease name] is usually normal.
* Extremities examination of patients with granulomatosis with polyangiitis is usually normal.
==References==
==References==
{{Reflist|2}}
{{Reflist|2}}

Latest revision as of 17:42, 11 April 2018

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Ali Poyan Mehr, M.D. [2]Associate Editor(s)-in-Chief: Amandeep Singh M.D.[3]Krzysztof Wierzbicki M.D. [4]

Overview

The important physical exam findings are Ulcerations, palpable purpura and subcutaneous nodules in the skin; conjunctivitis, uveitis, sinusitis, purulent exudate from nares,saddle nose deformity, reduced hearing in the head and neck; pleuritic chest pain ans signs of atelectasis in lung examination; and signs of mononeuritis multiplex on neural exam.

Physical Examination

  • Physical examination of patients with Granulomatosis with polyangiitis is usually remarkable for:[1][2]

Vital Signs

  • They usually have normal vital signs until infected.

Skin

The skin findings are seen in 14% of patients:[3]

HEENT

Neck

  • Neck examination of patients with granulomatosis with polyangiitis is usually normal.

Lungs

Examination may show signs of:

Heart

Abdomen

Back

  • Back examination of patients with granulomatosis with polyangiitis is usually normal.

Genitourinary

  • A pelvic/adnexal mass may be palpated
  • Inflamed mucosa

Neuromuscular

  • Patient is usually oriented to persons, place, and time
  • Mononeuritis multiplex[7]- Loss of sensory and motor functions
  • Cranial nerve paralysis

Extremities

  • Extremities examination of patients with granulomatosis with polyangiitis is usually normal.

References

  1. 1.0 1.1 Seo P, Stone JH (July 2004). "The antineutrophil cytoplasmic antibody-associated vasculitides". Am. J. Med. 117 (1): 39–50. doi:10.1016/j.amjmed.2004.02.030. PMID 15210387.
  2. Graves N (October 2006). "Wegener granulomatosis". Proc (Bayl Univ Med Cent). 19 (4): 342–4. PMC 1618758. PMID 17106496.
  3. Daoud MS, Gibson LE, DeRemee RA, Specks U, el-Azhary RA, Su WP (October 1994). "Cutaneous Wegener's granulomatosis: clinical, histopathologic, and immunopathologic features of thirty patients". J. Am. Acad. Dermatol. 31 (4): 605–12. PMID 8089286.
  4. Cannady SB, Batra PS, Koening C, Lorenz RR, Citardi MJ, Langford C, Hoffman GS (April 2009). "Sinonasal Wegener granulomatosis: a single-institution experience with 120 cases". Laryngoscope. 119 (4): 757–61. doi:10.1002/lary.20161. PMID 19263410.
  5. Genuis K, Pewarchuk J (September 2014). "Granulomatosis with polyangiitis (Wegener's) as a necrotizing gingivitis mimic: a case report". J Med Case Rep. 8: 297. doi:10.1186/1752-1947-8-297. PMC 4168997. PMID 25196320.
  6. Pagnoux C, Mahr A, Cohen P, Guillevin L (March 2005). "Presentation and outcome of gastrointestinal involvement in systemic necrotizing vasculitides: analysis of 62 patients with polyarteritis nodosa, microscopic polyangiitis, Wegener granulomatosis, Churg-Strauss syndrome, or rheumatoid arthritis-associated vasculitis". Medicine (Baltimore). 84 (2): 115–28. PMID 15758841.
  7. Anadure R, Narayanan C, Varadraj G, Nandeesh B (January 2017). "ANCA Associated Mononeuritis Multiplex with Overlap in Vasculitic Syndromes". J Clin Diagn Res. 11 (1): OD01–OD03. doi:10.7860/JCDR/2017/22252.9149. PMC 5324437. PMID 28273992.