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A Case of Henoch-Schoenlein Purpura with Necrotizing Vasculitis in the G-I Tract / 대한피부과학회지
Korean Journal of Dermatology ; : 748-751, 1998.
Article in Korean | WPRIM | ID: wpr-90032
ABSTRACT
Henoch-Schoenlein purpura is a syndrome of acute systemic allergic vasculitis involving the small vessels of skin and multiple organs, characterized by a symmetrical, non-thrombocytopenic, painless purpura, nephritis and gastrointestinal manifestations. Although GI involvement is about 70%, endoscopic and histopathological finding of the GI tract in Henoch-Schoenlein purpura is rarely reported and necrotizing vasculitis in GI tract biopsy has not been reported yet. We report a case of a 16-year-old male patient, who complained of palpable purpura, vomiting and epigastric pain with necrotizing vasculitis of the duodenum on histopathological examination.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Purpura / IgA Vasculitis / Skin / Vasculitis / Vomiting / Biopsy / Gastrointestinal Tract / Duodenum / Nephritis Limits: Adolescent / Humans / Male Language: Korean Journal: Korean Journal of Dermatology Year: 1998 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Purpura / IgA Vasculitis / Skin / Vasculitis / Vomiting / Biopsy / Gastrointestinal Tract / Duodenum / Nephritis Limits: Adolescent / Humans / Male Language: Korean Journal: Korean Journal of Dermatology Year: 1998 Type: Article