4.4 Review

Renal cell carcinoma: Evolving and emerging subtypes

Journal

WORLD JOURNAL OF CLINICAL CASES
Volume 1, Issue 9, Pages 262-275

Publisher

BAISHIDENG PUBLISHING GROUP INC
DOI: 10.12998/wjcc.v1.i9.262

Keywords

Renal cell carcinoma; Subtypes; Xp11 translocation; Mucinous tubular and spindle cell; Multilocular cystic clear cell; Carcinoma associated with neuroblastoma recently described entities; Clear cell papillary renal cell carcinoma; Acquired cystic kidney disease; Hereditary leiomyomatosis; Candidate entities; Renal cell carcinoma with t(6;11) translocation

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Our knowledge of renal cell carcinoma (RCC) is rapidly expanding. For those who diagnose and treat RCC, it is important to understand the new developments. In recent years, many new renal tumors have been described and defined, and our understanding of the biology and clinical correlates of these tumors is changing. Evolving concepts in Xp11 translocation carcinoma, mucinous tubular and spindle cell carcinoma, multilocular cystic clear cell RCC, and carcinoma associated with neuroblastoma are addressed within this review. Tubulocystic carcinoma, thyroid-like follicular carcinoma of kidney, acquired cystic disease-associated RCC, and clear cell papillary RCC are also described. Finally, candidate entities, including RCC with t(6;11) translocation, hybrid oncocytoma/chromophobe RCC, hereditary leiomyomatosis and RCC syndrome, and renal angiomyoadenomatous tumor are reviewed. Knowledge of these new entities is important for diagnosis, treatment and subsequent prognosis. This review provides a targeted summary of new developments in RCC. (C) 2013 Baishideng Publishing Group Co., Limited. All rights reserved.

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