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Korean Journal of Urology ; : 145-147, 2014.
Article in English | WPRIM | ID: wpr-29902

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.


Subject(s)
Female , Humans , Young Adult , Anemia, Sickle Cell , Carcinoma, Medullary , Carcinoma, Renal Cell , Hemoglobin, Sickle , Kidney Neoplasms , West Indies
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