| Literature DB >> 29089709 |
Mallika Tewari1, Shashikant Patne2, Richa Katiyar2, Dipanjan Biswas1, H S Shukla1.
Abstract
Diffuse serous cystic neoplasm (SCN) associated with pancreatic neuroendocrine tumor (PNET) is a rare finding reported previously in only three patients to the best of our knowledge. We herein present one such interesting report of a diffuse serous cystic adenoma (SCA) and co-existent PNET in a 25-year old lady who presented with abdominal pain for past 6 months. A triple-phase pancreatic protocol computed tomography (CT) scan revealed multiple cysts involving the entire pancreas. The cysts were thin walled, ranging from 2 to 8 cm in width, with no calcification or central scar that was confirmed at laparotomy. A frozen section revealed a neuroendocrine tumor and she underwent total pancreatectomy. Diffuse SCA with co-existent PNET infiltrating nerve bundles of the pancreatic parenchyma was made upon histopathology further verified by chromogranin-A immunostaining. The patient is insulin dependent and doing well at 2 years of follow-up. The origin of endocrine tumors from multipotent ductular stem cells has been suggested.Entities:
Keywords: Pancreatic neuroendocrine tumor; Pathology; Serous cystadenoma; Total pancreatectomy
Year: 2017 PMID: 29089709 PMCID: PMC5653579 DOI: 10.1007/s12262-017-1593-3
Source DB: PubMed Journal: Indian J Surg ISSN: 0973-9793 Impact factor: 0.656