Pancreatic solid serous cystadenoma: a rare entity that can lead to a futile surgery

Author:

Demesmaker Vincent1,Abou-Messaoud Faouzi1,Parent Muriel2,Vanhoute Bernard1,Maassarani Fadi1,Kothonidis Konstantinos1

Affiliation:

1. CHR Val de Sambre, Auvelais, Belgium

2. IPG, Gosselies, Belgium

Abstract

Abstract Although many types of pancreatic tumors exist, pancreatic solid serous cystadenoma stand as the most rare. Despite advances in medical imaging, definitive diagnosis remains complex. Here, we report a case of a 63-year-old man with a suspicious lesion of the pancreas discovered during a positron emission tomography–computed tomography. Despite an echo-endoscopy being performed, no biopsies were contributive. The magnetic resonance imaging did highlight another lesion in the liver. Due to the suspicion of a neuroendocrine tumor of the pancreas with liver metastases, a cephalic duodenopancreatectomy with partial hepatectomy was performed. During the procedure, another hepatic lesion was resected. The final histological diagnosis was a serous solid adenoma of the pancreas associated with a cholangiocarcinoma. During the follow-up, the patient presented a massive metastatic hepatic relapse even after the administration of a palliative chemotherapy.

Publisher

Oxford University Press (OUP)

Subject

Surgery

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