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- W1993717599 abstract "Pancreatic polypeptide-secreting tumors (PPoma) are extremely rare. In a large series of islet cell tumors, the frequency was only 3.7%.1 Moreover, the incidence of pure PPoma is estimated to be only 1% to 2% of all islet cell tumors.2 Because pancreatic polypeptide plays a limited physiologic role, clinical symptoms related to its hypersecretion are not obvious. Patients may thus present with advanced and/or metastatic disease. To our knowledge, 41 patients with PPoma have been reported since the first description by Larsson et al.3 in 1976, but about half of the patients could not undergo a curative operation. Recent advances in imaging technologies, however, have greatly contributed to detection of the nonfunctioning or clinically silent islet cell tumor. We herein describe a patient with a PPoma, in whom the diagnosis was made preoperatively by peroral pancreatoscopy (POPS) and endoscopic transpapillary biopsy. CASE REPORT" @default.
- W1993717599 created "2016-06-24" @default.
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- W1993717599 date "1998-07-01" @default.
- W1993717599 modified "2023-09-27" @default.
- W1993717599 title "A pancreatic polypeptide-secreting tumor of the pancreas diagnosed by peroral pancreatoscopy and endoscopic transpapillary biopsy" @default.
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- W1993717599 doi "https://doi.org/10.1016/s0016-5107(98)70135-x" @default.
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