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Mixed epithelial stromal renal tumor with dystrophic ossifi cation: a case report and literature review
Michael C. Large, Hikmat Al-Ahmadie, Arieh L. Shalhav,
Kevin C. Zorn
Section of Urology, University of Chicago Medical Center, Chicago, Illinois, USA
Address correspondence to Dr. Michael C. Large, University
of Chicago, Section of Urology, 5841 S. Maryland Avenue-MC6038, Chicago, IL 60637 USA
Canadian Journal of Urology 2009, 16(3), 4690-4693.
Abstract
A 25-year-old female presented with worsening right fl ank
pain and a 9 year history of a slow growing 4 centimeter
calcifi ed renal mass. The lesion was resected by laparoscopic
partial nephrectomy revealing a mixed epithelial and
stromal tumor (MEST). This tumor has unusual features
including the extensive amount of dystrophic calcifi cation
and the young age at presentation. Herein, we present a
focused review of the literature regarding MESTs, as well
as a discussion of calcifi ed renal mass management. We
conclude that laparoscopy may be utilized to safely perform
nephron sparing surgery for select, calcifi ed renal masses.
Keywords
mixed epithelial stromal tumor, calcifi cation, dystrophic ossifi cation, renal mass
Cite This Article
APA Style
Large, M.C., Al-Ahmadie, H., Shalhav, A.L., Zorn, K.C. (2009). Mixed epithelial stromal renal tumor with dystrophic ossifi cation: a case report and literature review. Canadian Journal of Urology, 16(3), 4690–4693.
Vancouver Style
Large MC, Al-Ahmadie H, Shalhav AL, Zorn KC. Mixed epithelial stromal renal tumor with dystrophic ossifi cation: a case report and literature review. Can J Urology. 2009;16(3):4690–4693.
IEEE Style
M.C. Large, H. Al-Ahmadie, A.L. Shalhav, and K.C. Zorn, “Mixed epithelial stromal renal tumor with dystrophic ossifi cation: a case report and literature review,” Can. J. Urology, vol. 16, no. 3, pp. 4690–4693, 2009.
Copyright © 2009 The Canadian Journal of Urology.