Paroxysmal drastic abdominal pain with tardive cutaneous lesions presenting in Henoch-Schnlein purpura

Henoch-Schnlein purpura（HSP） is a small-vessel vasculitis mediated by IgA-immune complex deposition.It is characterized by the clinical tetrad of non-thrombocytopenic palpable purpura,abdominal pain,arthritis and renal involvement.The diagnosis of HSP is difficult,especially when abdominal symptoms...

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Bibliographic Details
Published in:世界胃肠病学杂志：英文版 2012, Vol.18 (16), p.1991-1995
Main Author: Xiao-Liang Chen Hong Tian Jian-Zhong Li Jin Tao Hua Tang Yang Li Bin Wu
Format: Article
Language:English
Subjects:
SCH
病灶
皮肤过敏
紫癜
腹痛
血小板减少
迟发性
阵发性
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Summary:Henoch-Schnlein purpura（HSP） is a small-vessel vasculitis mediated by IgA-immune complex deposition.It is characterized by the clinical tetrad of non-thrombocytopenic palpable purpura,abdominal pain,arthritis and renal involvement.The diagnosis of HSP is difficult,especially when abdominal symptoms precede cutaneous lesions.We report a rare case of paroxysmal drastic abdominal pain with gastrointestinal bleeding presented in HSP.The diagnosis was verified by renal damage and the occurrence of purpura.
ISSN:1007-9327
2219-2840