Differentiating Polyarteritis nodosa from other diseases: Difference between revisions
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*[[Churg Strauss disease]] is characterized by hypereosinophilia and vasculitis like [[PAN]] in individuals with asthma and allergic nephritis. | *[[Churg Strauss disease]] is characterized by hypereosinophilia and vasculitis like [[PAN]] in individuals with asthma and allergic nephritis. | ||
*[[Henoch Schonlein purpura]] | *[[Henoch Schonlein purpura]] | ||
*Vasculitis secondary to connective tissue disorder | *[[Vasculitis]] secondary to [[connective tissue]] disorder | ||
*[[Cryoglobulinemic vasculitis]] | *[[Cryoglobulinemic vasculitis]] | ||
*[[Wegner's Granulomatosis]] | *[[Wegner's Granulomatosis]] | ||
Revision as of 19:22, 4 April 2017
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Polyarteritis nodosa Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Cafer Zorkun, M.D., Ph.D. [2]; Haritha Machavarapu, M.B.B.S.
Overview
Differentiating Polyarteritis Nodosa from other Diseases
- Microscopic polyangitis has clinical manifestations similar to PAN, but is characterized by presence of rapidly progressive glomerulonephritis and lung involvement unlike PAN.[1]
- Churg Strauss disease is characterized by hypereosinophilia and vasculitis like PAN in individuals with asthma and allergic nephritis.
- Henoch Schonlein purpura
- Vasculitis secondary to connective tissue disorder
- Cryoglobulinemic vasculitis
- Wegner's Granulomatosis
- Giantcell arteritis
- Infective endocarditis
- Mycotic aneurysm
- Atherosclerosis