Robert Ciortan, Loai Alshantti, Adrian Cîmpeanu, Mihai Toma, Monica Hortopan, Alexandru Procop, Gabriel Mitulescu, Sorin Petrea, Camelia Diaconu, Bogdan Gaspar, Lucian Pop, Valentin Varlas, Adrian Hasegan, Cristina Martac, Marilena Stoian, Anca Zgura, Gabriel Petre Gorecki, Irina Balescu, Alexandru Ciulcu, Nicolae Bacalbasa
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引用次数: 0
Abstract
Heterotopic pancreas is a rare congenital abnormality. The most common location is the stomach, duodenum and proximal jejunum. Rare locations are represented by the ampulla of Vater, esophagus, ileum, Meckel diverticulum, biliary tract, mesentery and spleen. We present the case of a 49 year old patient investigated for obstructive jaundice and diagnosed with an ampullar heterotopy of pancreas parenchyma, initially considered to be a malignant tumor. A Whipple pancreatoduodenectomy was performed with good postoperative evolution, the serum levels of bilirubin being normal after the first postoperative week.
期刊介绍:
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