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Review
. 2018 Dec 13;11(1):e226682.
doi: 10.1136/bcr-2018-226682.

Wolf in the sheep's clothing: intestinal angioedema mimicking infectious colitis

Affiliations
Review

Wolf in the sheep's clothing: intestinal angioedema mimicking infectious colitis

Asif Mehmood et al. BMJ Case Rep. .

Abstract

Hereditary angioedema (HAE) is a relatively rare clinical entity that can potentially cause life-threatening airway or intestinal oedema, patients with the latter usually presents with symptoms of gastroenteritis like vomiting, diarrhoea and abdominal pain. Here, we present a unique case of a less recognised type of HAE that is type III in a patient who presented with signs and symptoms consistent with infectious colitis. She previously had similar episodes and was managed multiple times with antibiotics, with no satisfactory response. There, she underwent extensive diagnostic evaluation. On the basis of findings of further investigations on the current visit, she was eventually diagnosed with intestinal angioedema. To the best of our knowledge, the present paper represents the third reported case of type III HAE-induced intestinal angioedema. Additionally, we undertake a literature review of HAE.

Keywords: gastroenterology; small intestine.

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Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
Abdominal contrast-enhanced CT scan showing edematous thickening of the intestinal wall (arrows).

References

    1. Habif TP. Clinical Dermatology E-Book: Elsevier Health Sciences, 2015.
    1. Kargarsharif F, Mehranmehr N, Zahedi Fard S, et al. . Type i and type ii hereditary angioedema: clinical and laboratory findings in Iranian Patients. Arch Iran Med 2015;18:425 doi:0151807/AIM.006 - PubMed
    1. Cichon S, Martin L, Hennies HC, et al. . Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III. Am J Hum Genet 2006;79:1098–104. 10.1086/509899 - DOI - PMC - PubMed
    1. van der Klooster JM, Schelfhout LJ, Grootendorst AF, et al. . [Recurrent attacks of angioedema ascribed to the use of estrogen preparations and a pregnancy (hereditary angioedema type 3)]. Ned Tijdschr Geneeskd 2002;146:1599–602. - PubMed
    1. Bork K, Barnstedt SE, Koch P, et al. . Hereditary angioedema with normal C1-inhibitor activity in women. Lancet 2000;356:213–217. 10.1016/S0140-6736(00)02483-1 - DOI - PubMed

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