Translocation Renal Cell Carcinoma t(6;11)(p21;q12) and Sickle Cell Anemia: First Report and Review of the Literature
Chaste Damien, Vian Emmanuel, Blanchet Pascal, Verhoest Gregory,
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( 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
KMID : 0358320140550020145
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.
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Hemoglobin SS; Kidney cancer; Renal cell carcinoma; Sickle cell anemia; Transcription factor EB
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