Hereditary angioedema presenting as irritable bowel syndrome: a case of early closure
Benrajab, Karim M.
- Publisher: Journal of Community Hospital Internal Medicine Perspectives
Journal of Community Hospital Internal Medicine Perspectives,
C4 | hereditary angioedema | C4; hereditary angioedema; IBS; abdominal pain; C1 esterase inhibitor | abdominal pain | Case Report | IBS | C1 esterase inhibitor
Abdominal pain is one of the most common reasons for outpatient and emergency department visits. We present one such case of early closure in a 32-year-old male with recurrent abdominal pain who was diagnosed with irritable bowel syndrome (IBS). Family history was suspicious for hereditary angioedema (HAE). The HAE workup came back positive, and the patient was started on prophylactic therapy, which led to an improvement in symptoms and quality of life. The purpose of this case is to create awareness among physicians to test for HAE in patients diagnosed with IBS who, based on their history or physical examination, have clinical suspicion for HAE.Keywords: C4; hereditary angioedema; IBS; abdominal pain; C1 esterase inhibitor(Published: 19 October 2015)Citation: Journal of Community Hospital Internal Medicine Perspectives 2015, 5: 29114 - http://dx.doi.org/10.3402/jchimp.v5.29114