摘要
嗜铬细胞瘤可分为遗传性和散发性两大类。基因突变在嗜铬细胞瘤的发生中起重要作用。对散发性嗜铬细胞瘤患者进行基因筛查，可以早期发现遗传性疾病，早期治疗。本文阐述了目前对散发性嗜铬细胞瘤基因筛查的临床进展及其意义。
[ Summary ] Most pheochromocytomas are sporadic cases while the rest occur as part of a hereditary cancer syndrome. Gene mutation plays a very important role in the development of pheochromocytoma. Gene screening in patients with sporadic pheochromocytomas could lead to early diagnosis of hereditary syndromes and more effective treatment. This review focuses on the recent advances and clinical significance of gene screening in sporadic pheochromocytomas.
出处
《中华内分泌代谢杂志》
CAS
CSCD
北大核心
2008年第1期91-93,共3页
Chinese Journal of Endocrinology and Metabolism
