1. Are Cystic Pancreatic Neuroendocrine Tumors an Indolent Entity Results from a Single-Center Surgical Series
- Author
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Riccardo De Robertis, Giovanni Marchegiani, Harmony Impellizzeri, Luca Landoni, Claudio Bassi, Anna Malpaga, Sara Cingarlini, G. Montagnini, Paola Capelli, Tommaso Pollini, Marco Miotto, Chiara Nessi, Mirko D'Onofrio, Letizia Boninsegna, Salvatore Paiella, Aldo Scarpa, Roberto Salvia, Giovanni Butturini, and Ilaria Posenato
- Subjects
Adult ,Male ,medicine.medical_specialty ,Cystic pancreatic neuroendocrine tumors ,Endocrinology, Diabetes and Metabolism ,Population ,Neuroendocrine tumors ,Single Center ,Postoperative outcome ,Young Adult ,03 medical and health sciences ,Cellular and Molecular Neuroscience ,0302 clinical medicine ,Endocrinology ,Internal medicine ,Solid pancreatic neuroendocrine tumors ,Single-center surgical series ,Clinical features ,medicine ,Humans ,Lack of knowledge ,Diagnostic Errors ,education ,Pathological ,Aged ,Aged, 80 and over ,education.field_of_study ,Endocrine and Autonomic Systems ,business.industry ,Middle Aged ,medicine.disease ,Tumor Burden ,Well differentiated ,Pancreatic Neoplasms ,Neuroendocrine Tumors ,030220 oncology & carcinogenesis ,Cohort ,Female ,030211 gastroenterology & hepatology ,Radiology ,Neoplasm Recurrence, Local ,Pancreatic Cyst ,business ,Follow-Up Studies - Abstract
Introduction: Cystic pancreatic neuroendocrine tumors (CPanNETs) represent an uncommon variant of pancreatic neuroendocrine tumors (PanNETs). Due to their rarity, there is a lack of knowledge with regard to clinical features and postoperative outcome. Methods: The prospectively maintained surgical database of a high-volume institution was queried, and 46 resected CPanNETs were detected from 1988 to 2015. Clinical, demographic, and pathological features and survival outcomes of CPanNETs were described and matched with a population of 92 solid PanNETs (SPanNETs) for comparison. Results: CPanNETs accounted for 7.8% of the overall number of resected PanNETs (46/587). CPanNETs were mostly sporadic (n = 42, 91%) and nonfunctioning (39%). Two functioning CPanNETs were detected (4.3%), and they were 2 gastrinomas. The median tumor diameter was 30 mm (range 10-120). All tumors were well differentiated, with 38 (82.6%) G1 and 8 (17.4%) G2 tumors. Overall, no CPanNET showed a Ki-67 >5%. A correct preoperative diagnosis of a CPanNET was made in half of the cases. After a median follow-up of >70 months, the 5- and 10-year overall survival of resected CPanNETs was 93.8 and 62.5%, respectively, compared to 92.7 and 84.6% for SPanNETs (p > 0.05). The 5- and 10-year disease-free survival rates were 94.5 and 88.2% for CPanNETs and 81.8 and 78.9% for SPanNETs, respectively (p > 0.05). Conclusion: In the setting of a surgical cohort, CPanNETs are rare, nonfunctional, and well-differentiated neoplasms. After surgical resection, they share the excellent outcome of their well-differentiated solid counterparts for both survival and recurrence.
- Published
- 2017
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