Abstract
First described in 1995 [1], renal medullary carcinoma (RMC) predominantly afflicts young adults and adolescents with sickle cell trait and is one of the most aggressive renal cell carcinomas [2, 3]. It arises from the renal papillae or calyceal epithelium of the renal medulla. In the original series by Davis et al. [1], the median overall survival of patients with RMC was only 4 months, and despite therapy it has only improved to 13 months in the most recent series of cases [3]. RMC is very rare, comprising <0.5% of all renal cell carcinomas [4], but its incidence is likely underestimated as it is a challenging diagnosis that can often be mistaken for collecting duct carcinoma or other aggressive kidney malignancies [5].
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Msaouel, P., Rao, P., Tannir, N.M. (2019). Renal Medullary Carcinoma. In: Malouf, G., Tannir, N. (eds) Rare Kidney Tumors. Springer, Cham. https://doi.org/10.1007/978-3-319-96989-3_6
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DOI: https://doi.org/10.1007/978-3-319-96989-3_6
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