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E-mail this article Sending… Your email has been sent. Another email has also been sent to your account, if you want to receive only one email from us, please add the email to your adblock list. If you do not receive our emails within 10 minutes, please check your spam folder, it may have been mistakenly marked as spam. We use cookies to personalise content and ads, to provide social media features and to analyse our traffic. We also share information about your use of our site with our social media, advertising and analytics partners. See details.Mullerian Duct Ductal Intraductal Papillary Mucinous Neoplasms of the Pancreas: A Clinicopathologic Study of 75 Cases. Mullerian duct-type intraductal papillary mucinous neoplasms (IPMNs) are a distinct entity in the spectrum of mucinous neoplasms in the pancreas. Although the histologic features are well established, the clinicopathologic and genetic characteristics of these tumors remain to be better defined. The purpose of this study was to characterize and update the clinicopathologic and genetic features of IPMNs involving the pancreas. All patients with an IPMN of the pancreas diagnosed in a tertiary care center from 2000 to 2016 were reviewed. Patients with mucinous cystic neoplasms without concurrent IPMN and patients with cystic neoplasms of the pancreas with concurrent IPMN were excluded. Seventy-five IPMNs diagnosed in the pancreas were identified. At diagnosis, patients were more likely to be male and had multifocal disease. Patients were more often symptomatic (74%) and often presented with elevated pancreatic enzymes (80%). Notably, cystic lesions were often attached to the pancreatic duct (63%), whereas invasive IPMN was accompanied by invasive carcinoma in 40% of cases. All patients underwent surgical resection of the pancreatic mass with histologically confirmed IPMN. The diagnosis of IPMN was confirmed based on the main histologic features in most cases (n = 62, 84%). In the remaining patients (n = 13, 16%), the diagnosis was based on histologic criteria and/or genetic testing, whereas both criteria were lacking in a single case. Intraductal papillary mucinous neoplasms of the pancreas were diagnosed in the setting of a background mucinous cystic neoplasm in 84% of