RT Journal Article
T1 Primary Pure Pancreatic -Type Acinar Cell Carcinoma of the Stomach: A Rare Entity with a Difficult Diagnosis and Review of the Literature
A1 Paseiro Crespo, Gloria Marta
A1 García Nebreda, María
A1 Roldán Cortés, David
A1 Peña Navarro, Itziar de la
A1 Álvaro Cifuentes, Edurne
A1 Marqués Medina, Elia
A1 Abad Motos, Ane
AB Acinar cell carcinoma is an uncommon tumour, representing only 1% to 2% of all exocrine pancreatic tumours. Pancreatic-type acinar cell carcinoma can occur in other organs, including the stomach, but it is extraordinarily rare. We report a case of a 51-year-old woman with a pancreatic-type pure acinar carcinoma of the stomach coexisting with a large cell B lymphoma synchronously, and a literature review of gastric carcinomas with pancreatic cell differentiation. At present there is a preoperative underdiagnosis of these tumours that could be minimized by including this entity in the differential diagnosis of gastric cancer and by performing immunohistochemical analysis with neuroendocrine markers and exocrine pancreatic enzymes.
PB SAGE Publications
SN 1066-8969
SN 1940-2465
YR 2022
FD 2022-01-24
LK https://hdl.handle.net/20.500.14352/114444
UL https://hdl.handle.net/20.500.14352/114444
LA eng
NO Paseiro-Crespo G, García-Nebreda M, Roldán Cortés D, De la Peña Navarro I, Álvaro Cifuentes E, Marqués Medina E, Abad-Motos A. Primary Pure Pancreatic -Type Acinar Cell Carcinoma of the Stomach: A Rare Entity with a Difficult Diagnosis and Review of the Literature. Int J Surg Pathol. 2022 Aug;30(5):528-538. doi: 10.1177/10668969211065763.
NO Research article
DS Docta Complutense
RD 9 abr 2025