| Literature DB >> 17029094 |
Yoshiki Sekijima1, Takao Hashimoto, Hiroshi Koshihara, Yasuhiro Kawachi, Fujio Otsuka, Shu-ichi Ikeda.
Abstract
We report a patient with hereditary angioedema (HAE) presenting with skin edema and abdominal pain. Laboratory examination showed reduced levels of CH50, C2, C4, and C1 inhibitor (C1-INH). Abdominal computed tomography (CT) showed marked mesenteric edema and wall thickening of the duodenum and transverse colon. Acute abdominal pain is common in HAE and is difficult to distinguish from surgical emergency. Massive mesenteric edema on CT is a rare, but specific, sign suggesting HAE.Entities:
Year: 2005 PMID: 17029094 DOI: 10.1007/s10165-005-0416-8
Source DB: PubMed Journal: Mod Rheumatol ISSN: 1439-7595 Impact factor: 3.023