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Published on: January 14, 2014
Primary primitive neuroectodermal tumor of the kidney. Case report and review of the literature
J Furman1, W M Murphy, P F Jelsma
1Department of Pathology, University of Florida, College of Medicine, Gainesville 32610, USA.
Abstract:
Small cell tumors are a heterogeneous group of neoplasms with similar morphologic features. They include lymphomas, carcinomas with variable degrees of neuroendocrine differentiation, rhabdomyosarcomas, and neuroblastomas. The authors describe a rare case of primitive neuroectodermal tumor (PNET) located in the kidney that was thoroughly studied with modern diagnostic techniques, including expression of protein P 30/32 MIC2 with the antibody 013 with subsequent demonstration of a genetic translocation consistent with t(11;22). The literature on small cell tumors of the kidney, with special emphasis on PNET, is reviewed.
Insights
This study details a rare kidney primitive neuroectodermal tumor (PNET), a type of small cell cancer. Diagnosis involved advanced techniques, confirming a specific genetic translocation t(11;22).
Area of Science:
- Oncology
- Pathology
- Genetics
Background:
- Small cell tumors represent a diverse group of neoplasms sharing similar morphological characteristics.
- These neoplasms encompass lymphomas, neuroendocrine carcinomas, rhabdomyosarcomas, and neuroblastomas.
- Primitive neuroectodermal tumors (PNETs) are rare, particularly in extraneural sites like the kidney.
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