Southeast Asian Journal of Case Report and Review

Online ISSN: 2319-1090

Southeast Asian Journal of Case Report and Review is a Peer-reviewed, International medical journal Published by the Association of Health Professionals. It will publish 04 issues per year will publish a research paper prepared by Health Professional. Journal will Give Preference to Case Report and Review Article   Aim and Scope The aim and commitment of the journal is to publish a research-oriented manuscript on significant issues in all the subjects and areas of Medical Science including Genome mutation and Pathogenicity in microbes. Journal more...

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Case Report


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113- 116


Authors Details

Yihan LI*


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Gastric neuroendocrine hyperplasia and dysplasia in a patient with Lynch Syndrome


Case Report

Author Details : Yihan LI*

Volume : 11, Issue : 4, Year : 2024

Article Page : 113-116

https://doi.org/10.18231/j.sajcrr.2024.027



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Abstract

Background: Lynch syndrome (LS), previously known as hereditary non-polyposis colorectal cancer (HNPCC), is an autosomal dominant disorder that predisposes individuals to various malignancies, most commonly adenocarcinomas. While low-grade neuroendocrine tumors (NETs) associated with Lynch syndrome are rarely reported, gastric neuroendocrine tumors (g-NETs) account for less than 1% of all gastric tumors.
Report: This case report presents a rare occurrence of gastric neuroendocrine hyperplasia and dysplasia in a 68-year-old female diagnosed with Lynch syndrome. The patient, previously treated for well-differentiated adenocarcinoma of the colon, was found to have a polyp in the gastric fundus during routine surveillance. Histological analysis revealed adenocarcinoma alongside neuroendocrine cell proliferation, confirmed by synaptophysin immunostaining.
Conclusion: This case highlights a novel association between Lynch syndrome and gastric neuroendocrine hyperplasia/dysplasia. This finding raises awareness among clinicians regarding Lynch syndrome in patients with low-grade NETs or neuroendocrine precursors and underscores the need for comprehensive surveillance and further research to understand the underlying mechanisms and clinical implications. It suggests that mutations in mismatch repair (MMR) deficiency may play a role in neuroendocrine cell proliferation, expanding the spectrum of Lynch syndrome-associated tumors, and pointing to new directions for studying the molecular pathways and pathogenesis of NETs.


Keywords: Lynch syndrome, Neuroendocrine neoplasm, Low grade, Hyperplasia, Dysplasia


How to cite : Yihan Li, Gastric neuroendocrine hyperplasia and dysplasia in a patient with Lynch Syndrome. South Asian J Case Rep Rev 2024;11(4):113-116

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