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[Rheumatology]Henoch-Schnolein purpura

저작시기 2005.12 | 등록일 2006.01.14 파워포인트파일 MS 파워포인트 (ppt) | 34페이지 | 가격 1,000원

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HS purpura에 대한 review of disease입니다.

목차

Introduction
Diagnostic criteria
Incidence
Etiology
Clinical feature
Treatment
Outcome

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Introduction
HS purpura was first recognized by Heberden in 1801.
An association between purpura and arthritis was described by Schonlein in 1837.
HS purpura is a small vessel vasculitis whose major manifestations include :
Arthritis
Nonthrombocytopenic purpura
Abdominal pain
Renal disease
One of the most common vasculitis of childhood.
Considered to be self-limiting.
Can continue to cause lifelong problems is
renal involvement.

Palpable purpura
Slightly raised “palpable hemorrhagic skin lesions.
Not related to thrombocytopenia.
Age < 20 onset of first symptoms
Bowel angina
Diffuse abdominal pain
Worse after meals
Diagnostic bowel ischemia(usually including diarrhea)
Histologic changes(wall granulocytes) in the walls of arterioles or venules.
※A patient shall be said to have HS purpura if at least 2 of 4 criteria are present. (sensitivity : 87.1% / specificity : 87.7%)

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