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Ulcerative colitis associated with chronic granulomatous disease: case report

Chronic Granulomatous Disease (CGD) is an inherited primary immunodeficiency disease which increases the body’s susceptibility to infections caused by certain bacteria and fungi. CGD is a rare disease, caused by four genes, one type is 1X linked and the other three are “autosomal recessive”. Althoug...

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Autores principales: Imanzade, Farid, Sayarri, Aliakbar, Tajik, Pantea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4553164/
https://www.ncbi.nlm.nih.gov/pubmed/26328046
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author Imanzade, Farid
Sayarri, Aliakbar
Tajik, Pantea
author_facet Imanzade, Farid
Sayarri, Aliakbar
Tajik, Pantea
author_sort Imanzade, Farid
collection PubMed
description Chronic Granulomatous Disease (CGD) is an inherited primary immunodeficiency disease which increases the body’s susceptibility to infections caused by certain bacteria and fungi. CGD is a rare disease, caused by four genes, one type is 1X linked and the other three are “autosomal recessive”. Although clinical presentation is variable, but characteristic features are recurrent pneumonia, lymphadenitis, hepatic or other abscesses. Gastrointestinal tract symptoms are common in x-linked recessive form of CGD. These include gastric and esophageal obstruction and inflammatory bowel disease. GI involvement including small and large intestines, the findings of luminal narrowing and the presence of granuloma can make it difficult to distinguish from Crohn’s disease. On the other hands according to the literature ulcerative colitis is rarely reported in patients with CGD. Our case presented with ulcerative colitis with CGD.
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spelling pubmed-45531642015-08-31 Ulcerative colitis associated with chronic granulomatous disease: case report Imanzade, Farid Sayarri, Aliakbar Tajik, Pantea Gastroenterol Hepatol Bed Bench Case Report Chronic Granulomatous Disease (CGD) is an inherited primary immunodeficiency disease which increases the body’s susceptibility to infections caused by certain bacteria and fungi. CGD is a rare disease, caused by four genes, one type is 1X linked and the other three are “autosomal recessive”. Although clinical presentation is variable, but characteristic features are recurrent pneumonia, lymphadenitis, hepatic or other abscesses. Gastrointestinal tract symptoms are common in x-linked recessive form of CGD. These include gastric and esophageal obstruction and inflammatory bowel disease. GI involvement including small and large intestines, the findings of luminal narrowing and the presence of granuloma can make it difficult to distinguish from Crohn’s disease. On the other hands according to the literature ulcerative colitis is rarely reported in patients with CGD. Our case presented with ulcerative colitis with CGD. Shaheed Beheshti University of Medical Sciences 2015 /pmc/articles/PMC4553164/ /pubmed/26328046 Text en ©2015 RIGLD, Research Institute for Gastroenterology and Liver Diseases This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Imanzade, Farid
Sayarri, Aliakbar
Tajik, Pantea
Ulcerative colitis associated with chronic granulomatous disease: case report
title Ulcerative colitis associated with chronic granulomatous disease: case report
title_full Ulcerative colitis associated with chronic granulomatous disease: case report
title_fullStr Ulcerative colitis associated with chronic granulomatous disease: case report
title_full_unstemmed Ulcerative colitis associated with chronic granulomatous disease: case report
title_short Ulcerative colitis associated with chronic granulomatous disease: case report
title_sort ulcerative colitis associated with chronic granulomatous disease: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4553164/
https://www.ncbi.nlm.nih.gov/pubmed/26328046
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