Vasculitis history and symptoms: Difference between revisions

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* [[Claudication]] of extremities
* [[Claudication]] of extremities
* New onset [[headache]] with localized tenderness - [[temporal arteritis]]
* New onset [[headache]] with localized tenderness - [[temporal arteritis]]
* Unexplained [[weight loss]] > 4 kg, [[Testicular pain]] - [[Polyarteritis nodosa]]
* Unexplained [[weight loss]] > 4 kg, [[testicular pain]] - [[Polyarteritis nodosa]]
* Nasal or oral inflammation (oral ulcers or purulent/bloody nasal discharge, may be painful) - [[Wegener's granulomatosis]]
* Nasal or oral inflammation (oral ulcers or purulent/bloody nasal discharge, may be painful) - [[Wegener's granulomatosis]]
* [[Asthma]] (history of [[wheezing]] or presently wheezing) - [[Churg-Strauss syndrome|Churg-Strauss arteritis]]
* [[Asthma]] (history of [[wheezing]] or presently wheezing) - [[Churg-Strauss syndrome|Churg-Strauss arteritis]]

Revision as of 15:09, 31 August 2012

Vasculitis

Overview

Classification

Large-sized vessel vasculitis
Takayasu's Arteritis
Temporal Arteritis
Medium-sized vessel vasculitis
Kawasaki's Disease
Polyarteritis Nodosa
Small-sized vessel vasculitis
Churg-Strauss Syndrome
Cutaneous leukocytoclastic vasculitis
Essential cryoglobulinemic vasculitis
Henoch-Schonlein Purpura
Microscopic polyangiitis
Wegener's Granulomatosis
Variable-sized vessel vasculitis
Sjogren syndrome
Cogan syndrome
Single organ vasculitis
Primary central nervous system angiitis

Causes

Differential Diagnosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: M.Umer Tariq [2]

Overview

History

A detailed history is important to elicit any recent medications, any risk of hepatitis infection, or any recent diagnosis with a connective tissue disorder such as systemic lupus erythematosus (SLE).

Symptoms

Patients usually present with systemic symptoms with single or multiorgan dysfunction.

Common (and nonspecific) complaints include

The following symptoms should raise a strong suspicion of a vasculitis:

  • Palpable purpura. If patients have this in isolation, it is most likely due to cutaneous leukocytoclastic vasculitis. If the purpura is in combination with systemic organ involvement, it is most likely to be Henoch-Schonlein purpura or microscopic polyarteritis.

Other relatively common symptoms include:

References

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