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C-Kit–positive metastatic malignant pigmented...
Journal article

C-Kit–positive metastatic malignant pigmented clear-cell epithelioid tumor arising from the kidney in a child without tuberous sclerosis

Abstract

We report the first pediatric case of malignant pigmented epithelioid clear-cell tumor arising from kidney; the lesion occurred in a 12-year-old girl without tuberous sclerosis. The tumor was widely metastatic to the retroperitoneum and chest, and the patient died of the disease 9 months after diagnosis, despite active chemotherapy. Pigmented epithelioid clear-cell tumor of the kidney is a rare variant of epithelioid angiomyolipoma and a member of the family of perivascular epithelioid cell tumors (PEComas). The tumor demonstrated overlapping features between clear-cell sugar tumor and epithelioid variant of angiomyolipoma. Tumor cells were positive for HMB-45 expression, negative for any evidence of muscular differentiation, and contained melanin pigment and premelanosomes in the cytoplasm. Diffuse C-Kit (CD117) positivity was identified throughout the tumor. This is the first report of C-Kit-positive malignant PEComas.

Authors

Yu W; Fraser RB; Gaskin DA; Fernandez CV; Wright JR

Journal

Annals of Diagnostic Pathology, Vol. 9, No. 6, pp. 330–334

Publisher

Elsevier

Publication Date

December 1, 2005

DOI

10.1016/j.anndiagpath.2005.04.003

ISSN

1092-9134

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