Renal Primitive Neuroectodermal Tumor or Renal Ewing Sarcoma
DOI:
https://doi.org/10.3329/kyamcj.v13i4.65086Keywords:
Ewing sarcoma family tumors, Extraskeletal Ewing sarcoma, Renal Ewing sarcoma, Renal primitive neuroectodermal tumor (Renal PNET)Abstract
Renal primitive neuroectodermal tumor (renal PNET) or renal Ewing sarcoma (renal ES) is a rare, rapidly growing malignant small round cell tumor with poor prognosis. A 32-years-old Bangladeshi male patient presented with right loin pain, fever and anemia. On CT imaging a large (18x10.5x10.0 cm) renal mass was discovered. On suspicion of malignancy, a biopsy was taken from the mass. Microscopic evaluation showed features consistent with malignant small round blue cell tumor. Immunohistochemical stains showed diffuse and strong positive reaction to CD-99 and negative for WT-1, CD-3 and CD-20, which confirmed the diagnosis of renal PNET. After 6 cycles of combined chemotherapy, the patient was relatively well and at 6 months follow-up he showed no evidence of metastasis or recurrence.
KYAMC Journal Vol. 13, No. 04, January 2023: 257-260
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