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10.1007/s13730-017-0259-0

http://scihub22266oqcxt.onion/10.1007/s13730-017-0259-0
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C5694397!5694397!28509141
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suck abstract from ncbi


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pmid28509141      CEN+Case+Rep 2017 ; 6 (2): 132-5
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  • Primary Ewing sarcoma of the kidney: a case report and treatment review #MMPMID28509141
  • Sadiq M; Ahmad I; Shuja J; Ahmad K
  • CEN Case Rep 2017[Nov]; 6 (2): 132-5 PMID28509141show ga
  • Ewing sarcomas/primitive neuroectodermal tumors (ES/PNET) of the kidney are rarely found high-grade malignant tumors, offering poor prognosis. Although established treatment guidelines for ES of kidney are scarce, a multi-modality treatment approached is typically implemented. Herein, we report a 14-year-old female patient with ES of right kidney. Post-nephrectomy disease recurrence was treated with chemotherapy (i.e., vincristine, doxorubicin and cyclophosphamide); marked reduction in tumor size (i.e., from 18.5 × 11.3 cm2 to 3.7 × 2.2 cm2; ~96% reduction in size) as per computed tomography images was observed. We present our treatment experience and review from the available literature.
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