Literature DB >> 18486406

A case of angioedema due to acquired C1 esterase inhibitor deficiency masquerading as suspected peritonitis: a case report.

Seong Bin Hong1, Cheol-Woo Kim, Ji Hye Kim, Jun Sig Kim, Seung Baik Han.   

Abstract

Angioedema due to acquired C1 esterase deficiency is a rare condition and a non-inflammatory disease characterized by episodes of edema of the mucosa of the upper airway or gastrointestinal tract. The purpose of this case report is to heighten awareness among emergency physicians of a peritonitis-like condition that can develop into angioedema due to acquired C1 esterase inhibitor deficiency, and thereby help to prevent false diagnosis resulting in unnecessary surgical intervention. We report the case of a 21-year-old man who presented to the Emergency Department (ED) with abdominal pain. He was later diagnosed with angioedema of the gastrointestinal tract due to acquired C1 esterase deficiency that was initially suspected as peritonitis. Careful evaluation of the acute abdomen in acquired C1 esterase deficiency is very important in the ED to distinguish between medical and surgical causes of an acute abdomen. Copyright Â
© 2011 Elsevier Inc. All rights reserved.

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Year:  2008        PMID: 18486406     DOI: 10.1016/j.jemermed.2008.04.004

Source DB:  PubMed          Journal:  J Emerg Med        ISSN: 0736-4679            Impact factor:   1.484


  1 in total

1.  Abdominal hereditary angio-oedema caught on magnetic resonance imaging.

Authors:  Mayven Tien Li Siow; Alexander Myles Robertson; Rohit R Ghurye; Paul A Blaker
Journal:  BMJ Case Rep       Date:  2021-12-31
  1 in total

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