Case Report
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World J Gastroenterol. Apr 28, 2011; 17(16): 2150-2154
Published online Apr 28, 2011. doi: 10.3748/wjg.v17.i16.2150
Celiac disease and microscopic colitis: A report of 4 cases
Zsolt Barta, Eva Zold, Arpad Nagy, Margit Zeher, Istvan Csipo
Zsolt Barta, Eva Zold, Arpad Nagy, Margit Zeher, Istvan Csipo, 3rd Department of Medicine, Institute for Internal Medicine, Medical and Health Science Center, University of Debrecen, 4032 Moricz Zs. krt. 22, Debrecen, Hungary
Author contributions: All authors gave substantial contributions to acquisition, analysis and interpretation of data and participated in writing the paper; Barta Z gave final approval of the version to be published.
Correspondence to: Zsolt Barta, MD, PhD, 3rd Department of Medicine, Institute for Internal Medicine, Medical and Health Science Center, University of Debrecen, 4032 Moricz Zs. krt. 22, Debrecen, Hungary. barta@dote.hu
Telephone: +36-52-255218 Fax: +36-52-255218
Received: October 27, 2010
Revised: December 30, 2010
Accepted: January 7, 2011
Published online: April 28, 2011
Abstract

Celiac disease (CD) is an autoimmune disorder of the small intestine that occurs in genetically predisposed people at all ages. However, it can be associated also to other immunopathological disorders, and may be associated with abnormal histology in segments of the gut other than the small bowel including colonic inflammation. While guidelines for endoscopic investigation of the jejunum are well defined, no indication is defined for colonic investigation. We describe four cases of concurrent CD and microscopic colitis (MC) diagnosed at our department over a 10-year period and analyzed the main features and outcomes of CD in this setting. The symptoms of these patients were improved initially by a gluten-free diet before the onset of MC symptoms. Two of the patients were siblings and had an atypical form of CD. The other two patients with CD and MC also presented with fibrosing alveolitis and were anti-Saccharomyces cerevisiae antibody positive. The co-existence of immune-mediated small bowel and colonic inflammatory and pulmonary diseases are not well-known, and no systematic approach has been used to identify the lifelong patterns of these immune-based diseases. Patients can develop, or present with CD at any stage in life, which can co-exist with other gastrointestinal diseases of (auto-) immune origin. In addition, the familial co-existence and prevalence of MC in patients with a prior diagnosis of CD are unclear. Clinicians managing celiac disease should be aware of these associations and understand when to consider colon investigation.

Keywords: Collagen colitis, Lymphocytic colitis, Celiac disease, Fibrosing alveolitis, Anti-saccharomyces cerevisiae antibody