A Rare Case of Well-Differentiated Neuroendocrine Tumor Arising From a Jejunal Pancreatic Heterotopia. (April 2021)

• Record Type: Journal Article
• Authors: Sappenfield, Ryan L.; Byrnes, Kathleen
• Is Part Of: International journal of surgical pathology. Volume 29:Number 2(2021)
• Page Start: 190
• Page End: 193
• Publication Date: 2021-04
• Subjects: neuroendocrine tumor -- heterotopic pancreas -- small intestine -- jejunum -- case report; Pathology, Surgical -- Periodicals; 617.07
• DOI: 10.1177/1066896920928126
• Languages: English
• ISSNs: 1066-8969

Abstract

Pancreatic heterotopia is a well-described entity occurring at multiple abdominal sites, most commonly the stomach and small intestine. They can develop similar disease processes as the pancreas ranging from acute pancreatitis, cyst formation, or neoplasms, most commonly ductal adenocarcinoma. Neuroendocrine tumors (NETs) arising in pancreatic heterotopias are exceedingly rare with only 3 prior published cases. In this article, we describe the first reported case of a NET arising in a jejunal pancreatic heterotopia in a 59-year-old woman presenting with abdominal pain and diarrhea. The submucosal tumor was composed of a well-differentiated NET (World Health Organization grade 1) directly intermixed with a heterotopic pancreas consisting of acinar cells, islet cells, and ducts. This case illustrates that NETs can occur in association with pancreatic heterotopias at any site. Also, the importance for pathologists to recognize that pancreatic heterotopias can give rise to a variety of neoplasms and is not limited to ductal adenocarcinoma.