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Pathology | Renal Tumors I - [click on image(s) below]

Clear Cell Sarcoma

  1. Age: 1-3 years
  2. Associations: none.
  3. This tumor is at least 10 times as likely to metastasize to bone as any other pediatric renal tumor, so it is sometimes referred to as the “bone metastasizing tumor of childhood”
  4. Clinical features: 66% of patients are male
  5. Gross: variable: may be homogeneous gray and lobular, or may be firm and light pink with whorled areas; usually well-circumscribed; bilaterality has not been reported
  6. Histology:
    • cells have lightly-staining cytoplasm (not optically clear as in renal cell carcinoma)
    • cells are arranged in cords or packets separated by fibrovascular septa with “chicken-wire” appearance
    • typically has infiltrative borders
  7. Prognosis: death rate = 30-40% with chemotherapy; late recurrences do occur.


 

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