Perivascular epithelioid cell tumor of the rectum: report of a case and review of the literature

World J Surg Oncol. 2014 Jan 13:12:12. doi: 10.1186/1477-7819-12-12.

Abstract

We report a case of perivascular epithelioid cell tumor arising in the rectum of a 55-year-old woman. The tumor was treated by transanal endoscopic microsurgery. After 1 year follow-up, the patient is alive with no radiologic or endoscopic evidence of recurrence. Perivascular epithelioid cell tumor is a rare mesenchymal tumor characterized by co-expression of melanocytic and smooth muscle markers. This rare tumor can arise in various organs, including the falciform ligament, uterus, uterine cervix, liver, kidney, lung, breast, cardiac septum, pancreas, prostate, thigh, and gastrointestinal tract. Perivascular epithelioid cell tumor of the gastrointestinal tract is very rare, with only 23 previously reported cases. We review the literature on perivascular epithelioid cell tumors arising in the gastrointestinal tract.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Female
  • Humans
  • Middle Aged
  • Perivascular Epithelioid Cell Neoplasms / pathology*
  • Perivascular Epithelioid Cell Neoplasms / surgery
  • Prognosis
  • Rectal Neoplasms / pathology*
  • Rectal Neoplasms / surgery