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A rare case of Crohn’s ileitis in a patient with constitutional mismatch repair deficiency
Constitutional mismatch repair deficiency (CMMRD), a variant of Lynch syndrome, is a rare disease characterized by café-au-lait spots, oligopolyposis, glioblastoma and lymphoma. A 24-year-old male, under surveillance for CMMRD, developed Crohn’s ileitis after total colectomy with end ileostomy for c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hellenic Society of Gastroenterology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411392/ https://www.ncbi.nlm.nih.gov/pubmed/28469372 http://dx.doi.org/10.20524/aog.2017.0129 |
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author | Kaimakliotis, Pavlos Giardiello, Francis Eze, Ogechukwu Truta, Brindusa |
author_facet | Kaimakliotis, Pavlos Giardiello, Francis Eze, Ogechukwu Truta, Brindusa |
author_sort | Kaimakliotis, Pavlos |
collection | PubMed |
description | Constitutional mismatch repair deficiency (CMMRD), a variant of Lynch syndrome, is a rare disease characterized by café-au-lait spots, oligopolyposis, glioblastoma and lymphoma. A 24-year-old male, under surveillance for CMMRD, developed Crohn’s ileitis after total colectomy with end ileostomy for colorectal cancer and failed to respond to oral corticosteroids. The patient underwent induction and maintenance of remission with vedolizumab infusions. We report the first patient with CMMRD developing Crohn’s disease. The choice of immunosuppressive therapy in these patients is challenging and needs to be made according to their risk for malignancy. |
format | Online Article Text |
id | pubmed-5411392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hellenic Society of Gastroenterology |
record_format | MEDLINE/PubMed |
spelling | pubmed-54113922017-05-03 A rare case of Crohn’s ileitis in a patient with constitutional mismatch repair deficiency Kaimakliotis, Pavlos Giardiello, Francis Eze, Ogechukwu Truta, Brindusa Ann Gastroenterol Case Report Constitutional mismatch repair deficiency (CMMRD), a variant of Lynch syndrome, is a rare disease characterized by café-au-lait spots, oligopolyposis, glioblastoma and lymphoma. A 24-year-old male, under surveillance for CMMRD, developed Crohn’s ileitis after total colectomy with end ileostomy for colorectal cancer and failed to respond to oral corticosteroids. The patient underwent induction and maintenance of remission with vedolizumab infusions. We report the first patient with CMMRD developing Crohn’s disease. The choice of immunosuppressive therapy in these patients is challenging and needs to be made according to their risk for malignancy. Hellenic Society of Gastroenterology 2017 2017-02-16 /pmc/articles/PMC5411392/ /pubmed/28469372 http://dx.doi.org/10.20524/aog.2017.0129 Text en Copyright: © Hellenic Society of Gastroenterology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kaimakliotis, Pavlos Giardiello, Francis Eze, Ogechukwu Truta, Brindusa A rare case of Crohn’s ileitis in a patient with constitutional mismatch repair deficiency |
title | A rare case of Crohn’s ileitis in a patient with constitutional mismatch repair deficiency |
title_full | A rare case of Crohn’s ileitis in a patient with constitutional mismatch repair deficiency |
title_fullStr | A rare case of Crohn’s ileitis in a patient with constitutional mismatch repair deficiency |
title_full_unstemmed | A rare case of Crohn’s ileitis in a patient with constitutional mismatch repair deficiency |
title_short | A rare case of Crohn’s ileitis in a patient with constitutional mismatch repair deficiency |
title_sort | rare case of crohn’s ileitis in a patient with constitutional mismatch repair deficiency |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411392/ https://www.ncbi.nlm.nih.gov/pubmed/28469372 http://dx.doi.org/10.20524/aog.2017.0129 |
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