Rare tumours of the pancreas: monocentric study
Astrid Bauschke, Annelore Altendorf-Hofmann, Aladdin Ali-Deeb, Michael Ardelt, Felix Dondorf, Falk Rauchfuss, Oliver Rohland, Aysun Tekbaș, Utz Settmacher

TL;DR
This study examines long-term survival and trends in rare pancreatic tumors, finding better outcomes compared to ductal pancreatic cancer.
Contribution
The study provides new insights into the long-term prognosis and increasing prevalence of rare pancreatic tumors over two decades.
Findings
The 5-year and 10-year survival rates for rare non-invasive pancreatic tumors were 72% and 55%, respectively.
The proportion of rare tumor entities increased significantly from 4.2% to 12.3% between 1999 and 2019.
Rare epithelial pancreatic tumors have a better long-term prognosis after surgery compared to ductal pancreatic cancer.
Abstract
The biology of rare pancreatic tumours, which differs from that of ductal pancreatic cancer, requires increased attention. Although the majority of rare pancreatic tumours are benign, it is difficult to decide whether an invasive component exists without complete removal of the lesion, despite considerable progress in diagnosis. We are investigating a large cohort of patients with histologically confirmed epithelial non-ductal non-neuroendocrine neoplasms of the pancreas. Here we analyze long-term survival from patients, who underwent resection of histologically confirmed epithelial non-ductal non-neuroendocrine neoplasms of the pancreas. At our department between Jan 1st, 1999, and Dec 31st, 2019. The median follow-up was 61 (range 0–168) month. All statistical analyses were performed using SPSS 26.0 (IBM, Chicago, IL, USA) software. 46 patients (48%) were followed up for more than 5…
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Taxonomy
TopicsPancreatic and Hepatic Oncology Research · Neuroendocrine Tumor Research Advances · Pancreatitis Pathology and Treatment
