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Reprogramming Pancreatic Ductal Adenocarcinoma to Pluripotency
Published on: February 2, 2024
[Pancreatic acinar cell carcinoma in a patient with familial adenomatous polyposis]
Belhassen Seket1, Jean-Christophe Saurin, Jean-Yves Scoazec
1Fédération des Spécialités Digestives, Hôpital E. Herriot, 69437 Lyon Cedex 03.
Abstract:
The relative risk of pancreatic cancer has been shown to be about 4 times that of the general population in familial adenomatous polyposis patients, but its frequency remains low, and the histological nature of these pancreatic tumors has been rarely reported. We describe the case of a 65-year-old patient, with a history of familial adenomatous polyposis coli, who developed advanced duodenal polyposis and a synchronous 25 mm tumor of the pancreatic isthmus. After total pancreatectomy and antrectomy, histological examination revealed an acinar cell carcinoma and duodenal adenomas with low and high-grade dysplasia, but no cancer. To our knowledge, this is the first description of the association of familial adenomatous polyposis with acinar cell carcinoma of the pancreas.
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