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A Case of Familial Appendiceal Neuroendocrine Tumor
The risk of developing appendiceal neuroendocrine tumor (aNET) may be attributed to multiple factors. A familial clustering is found in less than 1% of the cases. We report the case of a 25-year-old woman who initially presented with a clinical presentation of acute appendicitis and was subsequently...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419344/ https://www.ncbi.nlm.nih.gov/pubmed/37575490 http://dx.doi.org/10.14309/crj.0000000000001121 |
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author | Ghattas, Souad Hadeer, Ribal Aby Maalouf, Hani Al Bitar, Jad Younes, Ahmad Rahban, Hind El Rassi, Ziad |
author_facet | Ghattas, Souad Hadeer, Ribal Aby Maalouf, Hani Al Bitar, Jad Younes, Ahmad Rahban, Hind El Rassi, Ziad |
author_sort | Ghattas, Souad |
collection | PubMed |
description | The risk of developing appendiceal neuroendocrine tumor (aNET) may be attributed to multiple factors. A familial clustering is found in less than 1% of the cases. We report the case of a 25-year-old woman who initially presented with a clinical presentation of acute appendicitis and was subsequently diagnosed with aNET by histopathological examination after an emergency appendectomy. While revealing the result to the patient, she was found to have a positive family history of appendiceal carcinoid tumor. Although rare and only found in 1% of the cases, aNET found in family history should raise the suspicion of neuroendocrine tumors in other family members. |
format | Online Article Text |
id | pubmed-10419344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-104193442023-08-12 A Case of Familial Appendiceal Neuroendocrine Tumor Ghattas, Souad Hadeer, Ribal Aby Maalouf, Hani Al Bitar, Jad Younes, Ahmad Rahban, Hind El Rassi, Ziad ACG Case Rep J Case Report The risk of developing appendiceal neuroendocrine tumor (aNET) may be attributed to multiple factors. A familial clustering is found in less than 1% of the cases. We report the case of a 25-year-old woman who initially presented with a clinical presentation of acute appendicitis and was subsequently diagnosed with aNET by histopathological examination after an emergency appendectomy. While revealing the result to the patient, she was found to have a positive family history of appendiceal carcinoid tumor. Although rare and only found in 1% of the cases, aNET found in family history should raise the suspicion of neuroendocrine tumors in other family members. Wolters Kluwer 2023-08-11 /pmc/articles/PMC10419344/ /pubmed/37575490 http://dx.doi.org/10.14309/crj.0000000000001121 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 Ghattas, Souad Hadeer, Ribal Aby Maalouf, Hani Al Bitar, Jad Younes, Ahmad Rahban, Hind El Rassi, Ziad A Case of Familial Appendiceal Neuroendocrine Tumor |
title | A Case of Familial Appendiceal Neuroendocrine Tumor |
title_full | A Case of Familial Appendiceal Neuroendocrine Tumor |
title_fullStr | A Case of Familial Appendiceal Neuroendocrine Tumor |
title_full_unstemmed | A Case of Familial Appendiceal Neuroendocrine Tumor |
title_short | A Case of Familial Appendiceal Neuroendocrine Tumor |
title_sort | case of familial appendiceal neuroendocrine tumor |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419344/ https://www.ncbi.nlm.nih.gov/pubmed/37575490 http://dx.doi.org/10.14309/crj.0000000000001121 |
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