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An Unexpected Anemia Hiding a Rare Syndrome With Overlapping Phenotypes
Gastric polyposis is a rare endoscopic finding that can imply genetic syndromes predisposing to cancer development. Among the possible conditions associated with gastric polyposis and early onset gastric cancer (younger than 45 years) is juvenile polyposis syndrome. We present a clinical case of ear...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699651/ https://www.ncbi.nlm.nih.gov/pubmed/36447760 http://dx.doi.org/10.14309/crj.0000000000000926 |
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author | Dal Buono, Arianna Poliani, Laura Repici, Alessandro Hassan, Cesare Bianchi, Paolo |
author_facet | Dal Buono, Arianna Poliani, Laura Repici, Alessandro Hassan, Cesare Bianchi, Paolo |
author_sort | Dal Buono, Arianna |
collection | PubMed |
description | Gastric polyposis is a rare endoscopic finding that can imply genetic syndromes predisposing to cancer development. Among the possible conditions associated with gastric polyposis and early onset gastric cancer (younger than 45 years) is juvenile polyposis syndrome. We present a clinical case of early onset gastric cancer associated with a frameshift mutation in the gene SMAD4. Individuals carrying a pathogenic variant of this gene have a high risk of malignant transformation, especially of gastric cancer. Moreover, most of these patients present also with extraintestinal features of the hereditary hemorrhagic telangiectasia, and the first symptom prompting medical evaluation is anemia. |
format | Online Article Text |
id | pubmed-9699651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-96996512022-11-28 An Unexpected Anemia Hiding a Rare Syndrome With Overlapping Phenotypes Dal Buono, Arianna Poliani, Laura Repici, Alessandro Hassan, Cesare Bianchi, Paolo ACG Case Rep J Case Report Gastric polyposis is a rare endoscopic finding that can imply genetic syndromes predisposing to cancer development. Among the possible conditions associated with gastric polyposis and early onset gastric cancer (younger than 45 years) is juvenile polyposis syndrome. We present a clinical case of early onset gastric cancer associated with a frameshift mutation in the gene SMAD4. Individuals carrying a pathogenic variant of this gene have a high risk of malignant transformation, especially of gastric cancer. Moreover, most of these patients present also with extraintestinal features of the hereditary hemorrhagic telangiectasia, and the first symptom prompting medical evaluation is anemia. Wolters Kluwer 2022-11-24 /pmc/articles/PMC9699651/ /pubmed/36447760 http://dx.doi.org/10.14309/crj.0000000000000926 Text en © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Dal Buono, Arianna Poliani, Laura Repici, Alessandro Hassan, Cesare Bianchi, Paolo An Unexpected Anemia Hiding a Rare Syndrome With Overlapping Phenotypes |
title | An Unexpected Anemia Hiding a Rare Syndrome With Overlapping Phenotypes |
title_full | An Unexpected Anemia Hiding a Rare Syndrome With Overlapping Phenotypes |
title_fullStr | An Unexpected Anemia Hiding a Rare Syndrome With Overlapping Phenotypes |
title_full_unstemmed | An Unexpected Anemia Hiding a Rare Syndrome With Overlapping Phenotypes |
title_short | An Unexpected Anemia Hiding a Rare Syndrome With Overlapping Phenotypes |
title_sort | unexpected anemia hiding a rare syndrome with overlapping phenotypes |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699651/ https://www.ncbi.nlm.nih.gov/pubmed/36447760 http://dx.doi.org/10.14309/crj.0000000000000926 |
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