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Gastrointestinal Manifestations of CLOVES Syndrome
Congenital lipomatous overgrowth, vascular malformations, epidermal nevi, and scoliosis/skeletal/spinal anomalies (CLOVES) is a recently recognized syndrome. It is caused by somatic mutations in the PIK3CA gene that regulates cell growth and division. Although gastrointestinal manifestations of othe...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Wolters Kluwer
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171795/ https://www.ncbi.nlm.nih.gov/pubmed/37180463 http://dx.doi.org/10.14309/crj.0000000000001050 |
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author | St-Pierre, Joëlle Mirakhur, Anirudh Forbes, Nauzer |
author_facet | St-Pierre, Joëlle Mirakhur, Anirudh Forbes, Nauzer |
author_sort | St-Pierre, Joëlle |
collection | PubMed |
description | Congenital lipomatous overgrowth, vascular malformations, epidermal nevi, and scoliosis/skeletal/spinal anomalies (CLOVES) is a recently recognized syndrome. It is caused by somatic mutations in the PIK3CA gene that regulates cell growth and division. Although gastrointestinal manifestations of other PIK3CA-associated disorders have been described, they have not been well-characterized in CLOVES syndrome. We present a case report of a 34-year-old man with an established diagnosis of CLOVES syndrome who underwent a diagnostic colonoscopy for hematochezia and colonic wall thickening on imaging. Colonoscopy revealed widespread variceal-like submucosal lesions. Computed tomography/angiography showed the absence of the inferior mesenteric vein, impairing venous drainage. |
format | Online Article Text |
id | pubmed-10171795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-101717952023-05-11 Gastrointestinal Manifestations of CLOVES Syndrome St-Pierre, Joëlle Mirakhur, Anirudh Forbes, Nauzer ACG Case Rep J Case Report Congenital lipomatous overgrowth, vascular malformations, epidermal nevi, and scoliosis/skeletal/spinal anomalies (CLOVES) is a recently recognized syndrome. It is caused by somatic mutations in the PIK3CA gene that regulates cell growth and division. Although gastrointestinal manifestations of other PIK3CA-associated disorders have been described, they have not been well-characterized in CLOVES syndrome. We present a case report of a 34-year-old man with an established diagnosis of CLOVES syndrome who underwent a diagnostic colonoscopy for hematochezia and colonic wall thickening on imaging. Colonoscopy revealed widespread variceal-like submucosal lesions. Computed tomography/angiography showed the absence of the inferior mesenteric vein, impairing venous drainage. Wolters Kluwer 2023-05-10 /pmc/articles/PMC10171795/ /pubmed/37180463 http://dx.doi.org/10.14309/crj.0000000000001050 Text en © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Case Report St-Pierre, Joëlle Mirakhur, Anirudh Forbes, Nauzer Gastrointestinal Manifestations of CLOVES Syndrome |
title | Gastrointestinal Manifestations of CLOVES Syndrome |
title_full | Gastrointestinal Manifestations of CLOVES Syndrome |
title_fullStr | Gastrointestinal Manifestations of CLOVES Syndrome |
title_full_unstemmed | Gastrointestinal Manifestations of CLOVES Syndrome |
title_short | Gastrointestinal Manifestations of CLOVES Syndrome |
title_sort | gastrointestinal manifestations of cloves syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171795/ https://www.ncbi.nlm.nih.gov/pubmed/37180463 http://dx.doi.org/10.14309/crj.0000000000001050 |
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