Open Access
CASE REPORT
Multiple bilateral Perivascular Epithelioid Cell Tumor (PEComa) of the kidneys
Rahuldev Bhalla, David Dail, Paul Kozlowski, John Corman
Section of Urology & Renal Transplantation, Virginia Mason Medical Centre, Seattle, WA
Address correspondence to John M.Corman, MD, Section
of Urology & Renal Transplantation, Virginia Mason Medical
Centre, PO Box 900, Seattle, WA 98111 USA
Canadian Journal of Urology 2004, 11(3), 2296-2298.
Abstract
Perivascular Epithelial Cell (PEComa) Tumors are
extremely rare. These tumors are often regarded as low
grade Sarcomas and treated as such. We report a case of
a 70 year old female with a history of nonspecific
complaints and on routine CT scan had bilateral multiple
renal masses with no other extra renal disease. The largest
mass on the right was 11 cm x 7 cm x 11 cm and the left
there were multiple smaller masses. She underwent a
right radical nephrectomy that showed a PEComa and
an adjacent renal cell carcinoma. Her contralateral
kidney was followed for 3 years with no evidence of
growth or metastasis.
Keywords
perivascular epithelioid cell, PEComa, kidneys
Cite This Article
APA Style
Bhalla, R., Dail, D., Kozlowski, P., Corman, J. (2004). Multiple bilateral Perivascular Epithelioid Cell Tumor (PEComa) of the kidneys. Canadian Journal of Urology, 11(3), 2296–2298.
Vancouver Style
Bhalla R, Dail D, Kozlowski P, Corman J. Multiple bilateral Perivascular Epithelioid Cell Tumor (PEComa) of the kidneys. Can J Urology. 2004;11(3):2296–2298.
IEEE Style
R. Bhalla, D. Dail, P. Kozlowski, and J. Corman, “Multiple bilateral Perivascular Epithelioid Cell Tumor (PEComa) of the kidneys,” Can. J. Urology, vol. 11, no. 3, pp. 2296–2298, 2004.
Copyright © 2004 The Canadian Journal of Urology.