Pancreatic Neuroendocrine Tumor with Benign Serous Cystadenoma: A Rare Entity

Author:

Yadav Randhir Sagar1ORCID,Pokharel Ashik2,Shrestha Shumneva1ORCID,Pokharel Ashbita1,Gaire Deepshikha3,Pradhan Sumita2,Kansakar Prasan Bir Singh2

Affiliation:

1. Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal

2. Department of Gastrointestinal and General Surgery, Tribhuvan University Teaching Hospital, Kathmandu, Nepal

3. Department of Pathology, Tribhuvan University Teaching Hospital, Kathmandu, Nepal

Abstract

Mixed serous-neuroendocrine neoplasm constitutes pancreatic serous cystic neoplasms and pancreatic neuroendocrine tumor, two tumor components with different underlying pathologies. The differentiation of these tumors is important as the management and prognosis depend on the pancreatic neuroendocrine tumor component. We report a case of mixed serous-neuroendocrine neoplasm in a 47-year-old female who presented with epigastric pain abdomen for two years. Imaging studies, tumor markers, thorough systemic evaluation, surgical resection, histopathological examination, and timely follow-up constituted our management approach. A 4 cm × 4 cm mass in the distal pancreas with multiple cysts in the pancreatic parenchyma containing serous fluid on distal pancreatectomy and splenectomy was found. The histopathological examination revealed combined benign serous cystadenoma and neuroendocrine tumor. She did not have any recurrence or metastasis by four years of follow-up.

Publisher

Hindawi Limited

Subject

Oncology

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