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An official publication of the Middle-Eastern Association for Cancer Research
Clinical Cancer Investigation Journal
ISSN Print: 2278-1668, Online: 2278-0513
ARTICLE
Year: 2018   |   Volume: 7   |   Issue: 1   |   Page: 26-29     View issue

Primary Ewing's sarcoma/primitive neuroectodermal tumor of kidney: A rare case report


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Abstract

Ewing's sarcoma/primitive neuroectodermal tumor (ES/PNET) is a member of small round cell “blue tumor” family, occurring primarily in kidney is quite rare. Hence, detail appraisal is needed using histopathology, immunohistochemistry, and cytogenetic studies to attest the final diagnosis of ES/PNET, as this has an aggressive course and poor outcome. Here, we present a case of primary ES/PNET of kidney in 22-year-old male with locally invasive disease. Tumor cells were strongly positive for CD99 and FLI-1 on immunohistochemistry, thus confirming the final diagnosis.

Cite this article
Vancouver
Randale A, Parate S, Bhatkule M, Meshram S, Tathe S. Primary Ewing's sarcoma/primitive neuroectodermal tumor of kidney: A rare case report. Clin Cancer Investig J. 2018;7(1):26-9. https://doi.org/10.4103/ccij.ccij_68_17
APA
Randale, A., Parate, S., Bhatkule, M., Meshram, S., & Tathe, S. (2018). Primary Ewing's sarcoma/primitive neuroectodermal tumor of kidney: A rare case report. Clinical Cancer Investigation Journal, 7(1), 26-29. https://doi.org/10.4103/ccij.ccij_68_17

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ISSN Print: 2278-1668, Online: 2278-0513