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Autoimmune enteropathy: not all flat mucosa mean coeliac disease

A 62-year-old woman complaining of severe malabsorption was diagnosed with celiac disease based on the findings of flat, small intestinal mucosa and HLA-DQ2 positivity, although celiac serology was negative. This diagnosis was questioned due to the lack of clinical and histological improvement after...

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Autores principales: Volta, Umberto, Mumolo, Maria Gloria, Caio, Giacomo, Boschetti, Elisa, Latorre, Rocco, Giancola, Fiorella, Paterini, Paola, Giorgio, Roberto De
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4833853/
https://www.ncbi.nlm.nih.gov/pubmed/27099674
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author Volta, Umberto
Mumolo, Maria Gloria
Caio, Giacomo
Boschetti, Elisa
Latorre, Rocco
Giancola, Fiorella
Paterini, Paola
Giorgio, Roberto De
author_facet Volta, Umberto
Mumolo, Maria Gloria
Caio, Giacomo
Boschetti, Elisa
Latorre, Rocco
Giancola, Fiorella
Paterini, Paola
Giorgio, Roberto De
author_sort Volta, Umberto
collection PubMed
description A 62-year-old woman complaining of severe malabsorption was diagnosed with celiac disease based on the findings of flat, small intestinal mucosa and HLA-DQ2 positivity, although celiac serology was negative. This diagnosis was questioned due to the lack of clinical and histological improvement after a long period of strict gluten-free diet. The detection of enterocyte autoantibodies guided to the correct diagnosis of autoimmune enteropathy, leading to a complete recovery of the patient following an appropriate immunosuppressive treatment. Autoimmune enteropathy should be considered in the differential diagnosis of malabsorption with severe villous atrophy, including those cases with negative celiac-related serology.
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spelling pubmed-48338532016-04-20 Autoimmune enteropathy: not all flat mucosa mean coeliac disease Volta, Umberto Mumolo, Maria Gloria Caio, Giacomo Boschetti, Elisa Latorre, Rocco Giancola, Fiorella Paterini, Paola Giorgio, Roberto De Gastroenterol Hepatol Bed Bench Case Report A 62-year-old woman complaining of severe malabsorption was diagnosed with celiac disease based on the findings of flat, small intestinal mucosa and HLA-DQ2 positivity, although celiac serology was negative. This diagnosis was questioned due to the lack of clinical and histological improvement after a long period of strict gluten-free diet. The detection of enterocyte autoantibodies guided to the correct diagnosis of autoimmune enteropathy, leading to a complete recovery of the patient following an appropriate immunosuppressive treatment. Autoimmune enteropathy should be considered in the differential diagnosis of malabsorption with severe villous atrophy, including those cases with negative celiac-related serology. Shaheed Beheshti University of Medical Sciences 2016 /pmc/articles/PMC4833853/ /pubmed/27099674 Text en ©2016 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
Volta, Umberto
Mumolo, Maria Gloria
Caio, Giacomo
Boschetti, Elisa
Latorre, Rocco
Giancola, Fiorella
Paterini, Paola
Giorgio, Roberto De
Autoimmune enteropathy: not all flat mucosa mean coeliac disease
title Autoimmune enteropathy: not all flat mucosa mean coeliac disease
title_full Autoimmune enteropathy: not all flat mucosa mean coeliac disease
title_fullStr Autoimmune enteropathy: not all flat mucosa mean coeliac disease
title_full_unstemmed Autoimmune enteropathy: not all flat mucosa mean coeliac disease
title_short Autoimmune enteropathy: not all flat mucosa mean coeliac disease
title_sort autoimmune enteropathy: not all flat mucosa mean coeliac disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4833853/
https://www.ncbi.nlm.nih.gov/pubmed/27099674
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