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Translocation Renal Cell Carcinoma t(6;11)(p21;q12) and Sickle Cell Anemia: First Report and Review of the Literature

대한비뇨기과학회지 2014년 55권 2호 p.145 ~ 147
 ( Chaste Damien ) - Rennes University Hospital Department of Urology

 ( Vian Emmanuel ) - Pointe a Pitre University Hospital Department of Urology
 ( Blanchet Pascal ) - Pointe a Pitre University Hospital Department of Urology
 ( Verhoest Gregory ) - Rennes University Hospital Department of Urology

Abstract


Translocation renal cell carcinoma (RCC) is a family of rare tumors recently identified in the pediatric and young adult population. We report the first case of a young woman from French West Indies with sickle cell anemia who developed a translocation RCC t(6;11)(p21;q12). Usually people with the sickle cell condition are known to develop renal medullary carcinoma (RMC). To our knowledge, this is the first case described in the literature of a translocation RCC associated with sickle cell disease. Here we discuss the relation between translocation RCC, RMC, and sickle cell disease.

키워드

Hemoglobin SS; Kidney cancer; Renal cell carcinoma; Sickle cell anemia; Transcription factor EB
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