A Case of Henoch-Schonlein Purpura Complicated by Hemorrhagic Ascites / 대한류마티스학회지
The Journal of the Korean Rheumatism Association
;
: 417-421, 2004.
Article
in Korean
| WPRIM
| ID: wpr-24049
ABSTRACT
Henoch-Schonlein purpura (HSP) is a systemic vasculitis with IgA dominant immune complex deposits affecting small vessels in the skin, joint, gastrointestinal tract, and kidneys. Gastrointestinal symptoms are common and may precede the appearance of characteristic skin rash. These manifestations include abdominal pain, bleeding, bowel infarction, intussusception, or even, perforation. However, hemorrhagic ascites has been rarely described in patients with HSP. The pathophysiologic mechanism is presumably a vasculitis of the small vessels within the serosa. We report a 37-year-old man with HSP complicated by hemorrhagic ascites. Contrast CT of the abdomen showed extensive bowel wall thickening and ascites. A paracentesis yielded hemorrhagic fluid. These abdominal manifestations were improved after methylprednisolone pulse therapy.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Ascites
/
IgA Vasculitis
/
Serous Membrane
/
Skin
/
Vasculitis
/
Immunoglobulin A
/
Methylprednisolone
/
Abdominal Pain
/
Paracentesis
/
Gastrointestinal Tract
Limits:
Adult
/
Humans
Language:
Korean
Journal:
The Journal of the Korean Rheumatism Association
Year:
2004
Type:
Article
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