Mixed neuroendocrine-non-neuroendocrine tumors arising in residual gastric with multiple gene mutations: a case report

Read the full article See related articles

Discuss this preprint

Start a discussion What are Sciety discussions?

Listed in

This article is not in any list yet, why not save it to one of your lists.
Log in to save this article

Abstract

Background: Mixed Neuroendocrine-Non-Neuroendocrine Tumors (MiNENs) are a class of rare malignancies, and the pathogenesis remains obscure. The rarity of this condition has impeded the development of a standardized therapeutic approach. Case presentation: Here, we present the case of a patient diagnosed with gastric MiNENs post-gastrectomy, underwent a partial gastrectomy. The patient exhibited a complex genetic profile, marked by multiple gene mutations, and demonstrated elevated levels of Programmed Death Receptor Ligand 1 (PD-L1). The treatment regimen included etoposide, carboplatin, and sintilimab and the patient is currently in tumor-free survival. Conclusions: Our report shows that MiNENs could arise in residual gastric with multiple gene mutation, and surgery combining with chemotherapy and immunotherapy should be adopted.

Article activity feed