Perivascular Epithelioid Cell Tumor of the Retroperitoneum in a Young Woman Resulting in an Abdominal Chyloma

TE Lans, GH Ramshorst, John Hermans, Michael den Bakker, Khe Tran, G Kazemier

Research output: Contribution to journalArticleAcademicpeer-review

4 Citations (Scopus)
7 Downloads (Pure)


Perivascular epithelioid cell tumor (PEComa) is an extremely rare neoplasm which appears to have predominancy for young, frequently Asian, women. The neoplasm is composed chiefly of HMB-45-positive epithelioid cells with clear to granular cytoplasm and usually showing a perivascular distribution. These tumors have been reported in various organs under a variety of designations. Malignant PEComas exist but are very rare. The difficulty in determining optimal therapy, owing to the sparse literature available, led us to present this case. We report a retroperitoneal PEComa discovered during emergency surgery for abdominal pain in a 28-year-old Asian woman. The postoperative period was complicated by chylous ascites that was initially controlled by a wait-and-see policy with total parenteral nutrition. However, the chyle production gradually increased to more than 4 l per day. The development of a bacterial peritonitis resulted in cessation of production of abdominal fluid permitting normal nutrition without chylous leakage. Effective treatment for this rare complication of PEComa is not yet known; therefore, we have chosen to engage in long-term clinical follow-up.
Original languageUndefined/Unknown
Pages (from-to)389-392
Number of pages4
JournalJournal of Gastrointestinal Surgery
Issue number2
Publication statusPublished - 2009

Research programs

  • EMC MM-03-47-02-A
  • EMC NIHES-03-30-01

Cite this