Teratoid Wilms tumor is a rare variant of Wilms tumor composed predominantly of well-differentiated epithelial and/or mesenchymal heterologous elements. Like the classical Wilms tumor, this variant may also occur as a renal mass or may be found in extra renal locations. This tumor may be treated effectively by surgical resection; however, it generally fails to respond to chemotherapy. A review of the literature revealed 30 reported cases of intra renal and 5 reports of extra renal teratoid Wilms tumor. We report our experience with an additional three cases of renal teratoid Wilms tumor adding to the 30 cases previously reported.
CITATION STYLE
Ghamdi, D. A. L., Bakshi, N., & Akhtar, M. (2019). Teratoid wilms tumor: Report of three cases and review of the literature. Turk Patoloji Dergisi, 35(1), 61–68. https://doi.org/10.5146/tjpath.2016.01363
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