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Mixed Neuroendocrine Non-Neuroendocrine Neoplasm of the Ampulla of Vater: Report of a Rare Location.

作者信息

Rai Ankit, Varshney Vaibhav Kumar, Varshney Peeyush, Agarwal Lokesh, Rao Meenakshi, Agarwal Ayushi

机构信息

Department of Surgical Gastroenterology, All India Institute of Medical Sciences, Jodhpur, India.

Department of Pathology, All India Institute of Medical Sciences, Jodhpur, India.

出版信息

Ochsner J. 2025 Fall;25(3):209-213. doi: 10.31486/toj.25.0030.

Abstract

BACKGROUND

Mixed neuroendocrine non-neuroendocrine neoplasms (MiNENs) are rare tumors of the gastrointestinal tract with neuroendocrine and non-neuroendocrine components. Ampullary MiNENs are extremely rare, with few cases reported to date.

CASE REPORT

A 41-year-old male was diagnosed incidentally with a dilated common bile duct and intrahepatic biliary radicles while being evaluated for right ureteric calculi. Contrast-enhanced computed tomography scan of the abdomen showed a mass in the ampullary region with a positive double duct sign. Side-viewing endoscopy indicated an ampullary growth, and biopsy confirmed adenocarcinoma. The patient underwent total robotic pancreatoduodenectomy with an uneventful postoperative course. His final histopathologic examination revealed a tumor with 2 components, each of which accounted for at least 30% of the tumor: a neuroendocrine tumor and an adenocarcinoma with signet ring cells. The patient received adjuvant chemotherapy and at 1-year follow-up showed no evidence of recurrence.

CONCLUSION

Ampullary MiNENs are rare composite gastroenteropancreatic tumors characterized by histologic heterogeneity; they can be effectively treated with robotic pancreatoduodenectomy. The more aggressive component of the MiNEN should be considered when determining an adjuvant therapy.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/12456287/36d3e00cc852/toj-25-0030-figure1.jpg

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