Solid-Pseudopapillary Tumor of the Pancreas: A Single Center Experience

Aim of this study was to review the institutional experience of solid-pseudopapillary tumors of the pancreas with particular attention to the problems of preoperative diagnosis and treatment. From 1997 to 2013, SPT was diagnosed in 18 patients among 451 pancreatic cystic neoplasms (3.7%). All patien...

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Main Authors: Valentina Beltrame, Gioia Pozza, Enrico Dalla Bona, Alberto Fantin, Michele Valmasoni, Cosimo Sperti
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Gastroenterology Research and Practice
Online Access:http://dx.doi.org/10.1155/2016/4289736
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author Valentina Beltrame
Gioia Pozza
Enrico Dalla Bona
Alberto Fantin
Michele Valmasoni
Cosimo Sperti
author_facet Valentina Beltrame
Gioia Pozza
Enrico Dalla Bona
Alberto Fantin
Michele Valmasoni
Cosimo Sperti
author_sort Valentina Beltrame
collection DOAJ
description Aim of this study was to review the institutional experience of solid-pseudopapillary tumors of the pancreas with particular attention to the problems of preoperative diagnosis and treatment. From 1997 to 2013, SPT was diagnosed in 18 patients among 451 pancreatic cystic neoplasms (3.7%). All patients underwent preoperative abdominal ultrasound, computed assisted tomography, and tumor markers (CEA and CA 19-9) determinations. In some instances, magnetic resonance, positron emission tomography, and endoscopic ultrasound with aspiration cytology were performed. There were two males and 16 females. Serum CA 19-9 was slightly elevated in one case. Preoperative diagnosis was neuroendocrine tumor (n=2), mucinous tumor (n=2), and SPT (n=14). Two patients underwent previous operation before referral to our department: one explorative laparotomy and one enucleation of SPT resulting in surgical margins involvement. All patients underwent pancreatic resection associated with portal vein resection (n=1) or liver metastases (n=1). One patient died of metastatic disease, 77 months after operation, and 17 are alive and free with a median survival time of 81.5 months (range 36–228 months). Most of SPT can be diagnosed by CT or MRI, and the role of other diagnostic tools is very limited. We lack sufficient information regarding clinicopathologic features predicting prognosis. Caution is needed when performing limited resection, and long and careful follow-up is required for all patients after surgery.
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spelling doaj-art-998363b789b441ed9b8a97871c6de9582025-02-03T00:59:52ZengWileyGastroenterology Research and Practice1687-61211687-630X2016-01-01201610.1155/2016/42897364289736Solid-Pseudopapillary Tumor of the Pancreas: A Single Center ExperienceValentina Beltrame0Gioia Pozza1Enrico Dalla Bona2Alberto Fantin3Michele Valmasoni4Cosimo Sperti5Department of Surgery, Oncology and Gastroenterology, 3rd Surgical Clinic, University of Padua, Via Giustiniani 2, 35128 Padua, ItalyDepartment of Surgery, Oncology and Gastroenterology, 3rd Surgical Clinic, University of Padua, Via Giustiniani 2, 35128 Padua, ItalyDepartment of Surgery, Oncology and Gastroenterology, 3rd Surgical Clinic, University of Padua, Via Giustiniani 2, 35128 Padua, ItalyGastroenterology Unit, University of Padua, Via Giustiniani 2, 35128 Padua, ItalyDepartment of Surgery, Oncology and Gastroenterology, 3rd Surgical Clinic, University of Padua, Via Giustiniani 2, 35128 Padua, ItalyDepartment of Surgery, Oncology and Gastroenterology, 3rd Surgical Clinic, University of Padua, Via Giustiniani 2, 35128 Padua, ItalyAim of this study was to review the institutional experience of solid-pseudopapillary tumors of the pancreas with particular attention to the problems of preoperative diagnosis and treatment. From 1997 to 2013, SPT was diagnosed in 18 patients among 451 pancreatic cystic neoplasms (3.7%). All patients underwent preoperative abdominal ultrasound, computed assisted tomography, and tumor markers (CEA and CA 19-9) determinations. In some instances, magnetic resonance, positron emission tomography, and endoscopic ultrasound with aspiration cytology were performed. There were two males and 16 females. Serum CA 19-9 was slightly elevated in one case. Preoperative diagnosis was neuroendocrine tumor (n=2), mucinous tumor (n=2), and SPT (n=14). Two patients underwent previous operation before referral to our department: one explorative laparotomy and one enucleation of SPT resulting in surgical margins involvement. All patients underwent pancreatic resection associated with portal vein resection (n=1) or liver metastases (n=1). One patient died of metastatic disease, 77 months after operation, and 17 are alive and free with a median survival time of 81.5 months (range 36–228 months). Most of SPT can be diagnosed by CT or MRI, and the role of other diagnostic tools is very limited. We lack sufficient information regarding clinicopathologic features predicting prognosis. Caution is needed when performing limited resection, and long and careful follow-up is required for all patients after surgery.http://dx.doi.org/10.1155/2016/4289736
spellingShingle Valentina Beltrame
Gioia Pozza
Enrico Dalla Bona
Alberto Fantin
Michele Valmasoni
Cosimo Sperti
Solid-Pseudopapillary Tumor of the Pancreas: A Single Center Experience
Gastroenterology Research and Practice
title Solid-Pseudopapillary Tumor of the Pancreas: A Single Center Experience
title_full Solid-Pseudopapillary Tumor of the Pancreas: A Single Center Experience
title_fullStr Solid-Pseudopapillary Tumor of the Pancreas: A Single Center Experience
title_full_unstemmed Solid-Pseudopapillary Tumor of the Pancreas: A Single Center Experience
title_short Solid-Pseudopapillary Tumor of the Pancreas: A Single Center Experience
title_sort solid pseudopapillary tumor of the pancreas a single center experience
url http://dx.doi.org/10.1155/2016/4289736
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