Intraductal papillary mucinous neoplasms of the pancreas: an analysis of clinicopathologic features and outcome. Academic Article uri icon

Overview

abstract

  • OBJECTIVE: To define the natural history of resected intraductal papillary mucinous neoplasms (IPMN) of the pancreas and to identify clinical and pathologic prognostic features. SUMMARY BACKGROUND DATA: IPMN of the pancreas is a recently described pancreatic tumor. Because of a limited number of cases, prognostic factors and the natural history of resected cases have not been well defined. MATERIALS AND METHODS: A prospective pancreatic database was reviewed to identify patients with IPMN who were surgically managed. Pathologic re-review of each case was performed, and the clinicopathologic features were examined. Log rank and chi2 analysis were used to identify factors predictive of survival and recurrence. RESULTS: Over a 17-year period, 63 patients were identified. One patient was unresectable, 6 (10%) underwent a total pancreatectomy, and 56 (89%) had a partial pancreatectomy. Invasive carcinoma was present in 30 patients (48%). Transection margins were involved with atypia or carcinoma in 32 patients (51%). The median follow-up for survivors was 38 months. Disease-specific 5- and 10-year survival were 75% and 60%, respectively. Significant predictors of poor outcome included presentation with elevated bilirubin, presence of invasive carcinoma, increasing size and percentage of invasive carcinoma, histologic type of invasive carcinoma, positive lymph nodes, and vascular invasion. The presence of atypia or carcinoma in situ at the ductal resection margin was not associated with a poor outcome. CONCLUSIONS: Overall, IPMN has a favorable prognosis. Poor outcome in a subset of patients is largely the result of the presence, extent, and type of an invasive component, lymph node metastases, and vascular invasion.

publication date

  • March 1, 2004

Research

keywords

  • Adenocarcinoma, Mucinous
  • Carcinoma, Papillary
  • Pancreatic Neoplasms

Identity

PubMed Central ID

  • PMC1356240

Scopus Document Identifier

  • 1242341489

Digital Object Identifier (DOI)

  • 10.1097/01.sla.0000114132.47816.dd

PubMed ID

  • 15075659

Additional Document Info

volume

  • 239

issue

  • 3