Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.

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

´ëÇѺñ´¢±â°úÇÐȸÁö 2014³â 55±Ç 2È£ p.145 ~ 147
Chaste Damien, Vian Emmanuel, Blanchet Pascal, Verhoest Gregory,
¼Ò¼Ó »ó¼¼Á¤º¸
 ( 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.

Å°¿öµå

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

¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸

  

µîÀçÀú³Î Á¤º¸

KCI
KoreaMed
KAMS