A Rare Form of Chronic Granulomatous Disease (Type Iva) Presenting as Inflammatory Bowel Disease

Neutrophil dysfunction syndromes can sometimes mimic the clinical and pathological features of inflammatory bowel disease. The case of a 3.5-year-old boy with chronic diarrhea, abdominal pain, poor growth since infancy and microcytic, hypochromic anemia is presented. After an extensive diagnostic ev...

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Main Author: Francisco A Sylvester
Format: Article
Language:English
Published: Wiley 1996-01-01
Series:Canadian Journal of Gastroenterology
Online Access:http://dx.doi.org/10.1155/1996/717396
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author Francisco A Sylvester
author_facet Francisco A Sylvester
author_sort Francisco A Sylvester
collection DOAJ
description Neutrophil dysfunction syndromes can sometimes mimic the clinical and pathological features of inflammatory bowel disease. The case of a 3.5-year-old boy with chronic diarrhea, abdominal pain, poor growth since infancy and microcytic, hypochromic anemia is presented. After an extensive diagnostic evaluation, he was found to have a rare variant (type IVA) of chronic granulomatous disease. His gastrointestinal symptoms markedly improved during therapy with gamma-interferon. Chronic granulomatous disease can present initially with a clinical picture suggestive of chronic intestinal inflammation. Therefore it should be considered in the differential diagnosis of atypical inflammatory bowel disease, both in children and young adults.
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spelling doaj-art-6c85764aa5044cf38c73a09ba362994e2025-02-03T07:24:48ZengWileyCanadian Journal of Gastroenterology0835-79001996-01-0110422122410.1155/1996/717396A Rare Form of Chronic Granulomatous Disease (Type Iva) Presenting as Inflammatory Bowel DiseaseFrancisco A Sylvester0Division of Gastroenterology & Nutrition and Research Institute, The Hospital for Sick Children and the University of Toronto, Toronto, Ontario, CanadaNeutrophil dysfunction syndromes can sometimes mimic the clinical and pathological features of inflammatory bowel disease. The case of a 3.5-year-old boy with chronic diarrhea, abdominal pain, poor growth since infancy and microcytic, hypochromic anemia is presented. After an extensive diagnostic evaluation, he was found to have a rare variant (type IVA) of chronic granulomatous disease. His gastrointestinal symptoms markedly improved during therapy with gamma-interferon. Chronic granulomatous disease can present initially with a clinical picture suggestive of chronic intestinal inflammation. Therefore it should be considered in the differential diagnosis of atypical inflammatory bowel disease, both in children and young adults.http://dx.doi.org/10.1155/1996/717396
spellingShingle Francisco A Sylvester
A Rare Form of Chronic Granulomatous Disease (Type Iva) Presenting as Inflammatory Bowel Disease
Canadian Journal of Gastroenterology
title A Rare Form of Chronic Granulomatous Disease (Type Iva) Presenting as Inflammatory Bowel Disease
title_full A Rare Form of Chronic Granulomatous Disease (Type Iva) Presenting as Inflammatory Bowel Disease
title_fullStr A Rare Form of Chronic Granulomatous Disease (Type Iva) Presenting as Inflammatory Bowel Disease
title_full_unstemmed A Rare Form of Chronic Granulomatous Disease (Type Iva) Presenting as Inflammatory Bowel Disease
title_short A Rare Form of Chronic Granulomatous Disease (Type Iva) Presenting as Inflammatory Bowel Disease
title_sort rare form of chronic granulomatous disease type iva presenting as inflammatory bowel disease
url http://dx.doi.org/10.1155/1996/717396
work_keys_str_mv AT franciscoasylvester arareformofchronicgranulomatousdiseasetypeivapresentingasinflammatoryboweldisease
AT franciscoasylvester rareformofchronicgranulomatousdiseasetypeivapresentingasinflammatoryboweldisease