Retroperitoneal paraganglioma: single-institution experience and review of the literature

J Gastrointest Surg. 2006 Sep-Oct;10(8):1156-63. doi: 10.1016/j.gassur.2006.05.004.

Abstract

Paragangliomas are rare tumors arising from extra-adrenal chromaffin cells. We examined the clinical characteristics of all patients at our institution having paragangliomas resected from 1984 through 2005. Of 253 resections, 22 (9%) were retroperitoneal and were selected for further study. The ratio of males to females was 1.3:1, and the median age was 39 years. The average size, rate of metastasis (i.e., malignancy), and rate of function was 7.4 cm, 9.5%, and 57.1%, respectively. Tumors larger than 7 cm were more likely to require adjacent organ resection (P = 0.01). The overall 5-year survival was 73%. Survival was significantly worse after metastasis (P = 0.0023) but did not depend on the tumor diameter, the secreting function of the tumor, the status of surgical margins of resection, or status of the resected lymph nodes.

Publication types

  • Review

MeSH terms

  • Digestive System Surgical Procedures / methods*
  • Humans
  • Paraganglioma* / mortality
  • Paraganglioma* / surgery
  • Prognosis
  • Retroperitoneal Neoplasms* / mortality
  • Retroperitoneal Neoplasms* / surgery
  • Survival Rate