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Congenital “clear cell sarcoma of the kidney”

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Abstract

At 31 weeks gestation, a hydropic male fetus died in utero with metastatic disease from a renal clear cell sarcoma. The tumor had metastasized to para–aortic and mediastinal lymph nodes, lung, pleura, and liver, leading to superior vena cava obstruction and pulmonary hypoplasia. The pathologic findings and cytogenetic analysis of the fetus and tumor are presented. In addition, review of the literature reveals six other cases aged <6 months of age, including two extrarenal cases.

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Acknowledgements

The author wishes to thank Spencer Walker for his expert technical assistance.

Author information

Correspondence to Noelyn Anne Hung.

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Hung, N.A. Congenital “clear cell sarcoma of the kidney”. Virchows Arch 446, 566–568 (2005). https://doi.org/10.1007/s00428-005-1253-z

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Keywords

  • Clear cell sarcoma kidney
  • Congenital
  • Metastatic
  • Cytogenetics