Renal Tumors in Children / 임상소아혈액종양
Clinical Pediatric Hematology-Oncology
;
: 21-36, 2017.
Artículo
en Coreano
| WPRIM
| ID: wpr-197959
ABSTRACT
Pediatric renal tumors represent a diverse group, which include Wilms' tumor (WT), renal cell carcinoma (RCC), clear cell sarcoma of the kidney (CCSK), congenital mesoblastic nephroma, malignant rhabdoid tumor of the kidney (MRTK) and primitive neuroectodermal tumor. WT (85%) and RCC (8%) are the most prevalent types. WT predominates among the 1- to 10-year age group, but RCC exceeds WT in children over age 10 years. Pediatric renal tumors are genetically, histologically and clinically heterogeneous. The overall survival for children with localized WT is currently more than 90%, whereas poorer survival rates are observed for anaplastic WT, metastatic WT, metastatic CCSK, MRTK, metastatic RCC and relapsed WT. Therefore risk-stratified treatment is important to minimize treatment morbidity while preserving survival. This review focuses on distinct characteristics of each tumor type and optimal stratified treatment.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Carcinoma de Células Renales
/
Tasa de Supervivencia
/
Sarcoma de Células Claras
/
Tumor Rabdoide
/
Tumores Neuroectodérmicos Primitivos
/
Nefroma Mesoblástico
/
Tumor de Wilms
/
Riñón
Límite:
Niño
/
Humanos
Idioma:
Coreano
Revista:
Clinical Pediatric Hematology-Oncology
Año:
2017
Tipo del documento:
Artículo
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