A Case of Familial Appendiceal Neuroendocrine Tumor

Author:

Ghattas Souad1,Hadeer Ribal Aby1,Maalouf Hani1,Al Bitar Jad1,Younes Ahmad1,Rahban Hind2,El Rassi Ziad3

Affiliation:

1. Department of General Surgery, Saint Georges Hospital University Medical Center, Balamand University, Beirut, Lebanon

2. Department of Laboratory Medicine, Lebanese American University Medical Center, Beirut, Lebanon

3. Head of General Surgery Department, Saint George Hospital University Medical Center, Beirut, Lebanon

Abstract

ABSTRACT 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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference12 articles.

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3. One hundred years after “carcinoid”: Epidemiology of and prognostic factors for neuroendocrine tumors in 35,825 cases in the United States;Yao;J Clin Oncol.,2008

4. Epidemiology of neuroendocrine tumors of the appendix in the USA: A population-based national study (2014-2019);Alkhayyat;Ann Gastroenterol.,2021

5. Familial syndromes associated with neuroendocrine tumours;Gut;Contemp Oncol (Pozn).,2015

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