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Hereditary angioedema presenting as irritable bowel syndrome: a case of early closure

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 angioedem...

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Detalles Bibliográficos
Autores principales: Benrajab, Karim M., Singh, Gurkeerat, Obah, Eugene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4612482/
https://www.ncbi.nlm.nih.gov/pubmed/26486119
http://dx.doi.org/10.3402/jchimp.v5.29114
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author Benrajab, Karim M.
Singh, Gurkeerat
Obah, Eugene
author_facet Benrajab, Karim M.
Singh, Gurkeerat
Obah, Eugene
author_sort Benrajab, Karim M.
collection PubMed
description 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.
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spelling pubmed-46124822015-11-23 Hereditary angioedema presenting as irritable bowel syndrome: a case of early closure Benrajab, Karim M. Singh, Gurkeerat Obah, Eugene J Community Hosp Intern Med Perspect Case Report 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. Co-Action Publishing 2015-10-19 /pmc/articles/PMC4612482/ /pubmed/26486119 http://dx.doi.org/10.3402/jchimp.v5.29114 Text en © 2015 Karim M. Benrajab et al. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Benrajab, Karim M.
Singh, Gurkeerat
Obah, Eugene
Hereditary angioedema presenting as irritable bowel syndrome: a case of early closure
title Hereditary angioedema presenting as irritable bowel syndrome: a case of early closure
title_full Hereditary angioedema presenting as irritable bowel syndrome: a case of early closure
title_fullStr Hereditary angioedema presenting as irritable bowel syndrome: a case of early closure
title_full_unstemmed Hereditary angioedema presenting as irritable bowel syndrome: a case of early closure
title_short Hereditary angioedema presenting as irritable bowel syndrome: a case of early closure
title_sort hereditary angioedema presenting as irritable bowel syndrome: a case of early closure
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4612482/
https://www.ncbi.nlm.nih.gov/pubmed/26486119
http://dx.doi.org/10.3402/jchimp.v5.29114
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