%0 Journal Article
%T 家族性嗜铬细胞瘤诊治进展<br>Progress in Diagnosis and Treatment of Familial Pheochromocytoma
%A 袁洋
%A 张荣贵
%A 李俊伍
%A 解晓都
%A 闫九松
%J Advances in Clinical Medicine
%P 8020-8025
%@ 2161-8720
%D 2023
%I Hans Publishing
%R 10.12677/ACM.2023.1351123
%X 家族性嗜铬细胞瘤(Familial Pheochromocytoma, FP)是常染色体显性遗传病，家族性嗜铬细胞瘤可伴随某些遗传性综合征如：家族性视网膜及中枢性神经系统血管瘤病(Von-Hippel-Lindau disease，VHL病)，多发内分泌肿瘤2型(MEN2)，家族性副神经节瘤1~5型，神经纤维瘤病1型等，本文详细阐述了上述相关疾病与家族性嗜铬细胞瘤的相关性，对家族性嗜铬细胞瘤最新研究进展进行综述。<br />
Familial pheochromocytoma (FP) is an autosomal dominant disorder. Familial pheochromocytoma can be accompanied by certain genetic syndromes such as familial retinal and central nervous sys-tem angiomatosis (VHL disease), multiple endocrine neoplasia type 2 (MEN2), familial paragangli-oma type 1~5, neurofibromatosis type 1, and so on, This article describes in detail the correlation between the above related diseases and familial pheochromocytoma, and reviews the latest re-search progress in familial pheochromocytoma.
%K 家族性嗜铬细胞瘤，多发内分泌肿瘤2型，VHL<br>Familial Pheochromocytoma
%K Multiple Endocrine Neoplasia Type 2
%K VHL
%U http://www.hanspub.org/journal/PaperInformation.aspx?PaperID=65569