毛囊素
Birt-Hogg-Dubé综合征
医学
癌症综合征
病理
考登综合征
结节性硬化
肾癌
肾细胞癌
癌症
癌变
癌症研究
种系突变
BAP1型
肾
突变
生物
基因
内科学
遗传学
放射科
气胸
作者
Michel Alchoueiry,Kristine M. Cornejo,Elizabeth P. Henske
标识
DOI:10.1053/j.semdp.2023.11.002
摘要
Multiple hereditary syndromes predispose to kidney cancer, including Von Hippel-Lindau syndrome, BAP1-Tumor Predisposition Syndrome, Hereditary Papillary Renal Cell Carcinoma, Tuberous Sclerosis Complex, Birt-Hogg-Dubé syndrome, Hereditary Paraganglioma–Pheochromocytoma Syndrome, Fumarate Hydratase Tumor Predisposition Syndrome, and Cowden syndrome. In some cases, mutations in the genes that cause hereditary kidney cancer are tightly linked to similar histologic features in sporadic RCC. For example, clear cell RCC occurs in the hereditary syndrome VHL, and sporadic ccRCC usually has inactivation of the VHL gene. In contrast, mutations in FLCN, the causative gene for Birt-Hogg-Dube syndrome, are rarely found in sporadic RCC. Here, we focus on the genes and pathways that link hereditary and sporadic RCC.
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