Pathologically confirmed pancreatic hamartoma after surgical resection with an aldosterone-producing adrenal tumor: a case report

Author:

Kim Jae Han1ORCID,Yoon Seung Hyun1,Choi Ji Ahn1,Kwak Ji Hyeon1,Kim Milim23,Kim Sung Hyun4ORCID

Affiliation:

1. Yonsei University College of Medicine, Severance Hospital, Yonsei University Health System , Seoul 03722, The Republic of Korea

2. Department of Pathology , Severance Hospital, , Seoul 03722, The Republic of Korea

3. Yonsei University College of Medicine , Severance Hospital, , Seoul 03722, The Republic of Korea

4. Department of Hepatobiliary and Pancreatic Surgery, Yonsei University College of Medicine , Seoul 03722, The Republic of Korea

Abstract

Abstract Pancreatic hamartoma is a benign tumor of the pancreas with an extremely low incidence and is commonly diagnosed by pathologic examination after surgery. This report describes the case of a 57-year-old female who was referred for the evaluation of a pancreatic mass and an adrenal incidentaloma. Further imaging studies suggested pancreatic neuroendocrine tumor and aldosterone-producing adrenal tumor. Pylorus-preserving pancreaticoduodenectomy was performed with the initial impression of a pancreatic neuroendocrine tumor. However, pathology results revealed a pancreatic hamartoma. Multiple endocrine neoplasia type 1 syndrome was discussed as a probable explanation for tumor masses in both the pancreas and adrenal gland.

Publisher

Oxford University Press (OUP)

Subject

Surgery

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