| Literature DB >> 30567241 |
Asif Mehmood1, Hafez Mohammad Ammar Abdullah2, Faisal Inayat3, Waqas Ullah1.
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. © BMJ Publishing Group Limited 2018. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: gastroenterology; small intestine
Mesh:
Year: 2018 PMID: 30567241 PMCID: PMC6301529 DOI: 10.1136/bcr-2018-226682
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X