家族性高三酰甘油血症诊断标准及鉴别诊断  

Diagnostic Criteria and Differential Diagnosis of Familial Hypertriglyceridemia

作　　者：刘维娟[1] 周珊珊[1] 何津春[1,2] 严祥[3] 

机构地区：[1]兰州大学第一临床医学院,兰州730000 [2]兰州大学第一医院医学检验中心,兰州730000 [3]兰州大学第一医院老年病科,兰州730000

出　　处：《医学综述》2014年第17期3089-3091,共3页Medical Recapitulate

基　　金：国家"十五"重大科技专项(2002DA711A028-17);教育部科技基础平台建设(505015)

摘　　要：家族性高三酰甘油血症(FHTG)为原发性疾病,表现为单纯性三酰甘油升高。最早诊断标准为先证者三酰甘油升高;家系至少两个一级亲属患病;排除继发性高三酰甘油血症。随着研究的深入,其诊断标准也在不断增加,最新的诊断标准中加入总载脂蛋白B水平。FHTG的确诊还需与其他原发及继发性高三酰甘油血症相鉴别。该文就FHTG的临床诊断标准及鉴别诊断进行综述。Familial hypertriglyceridemia（FHTG） is a primary disease ,characterized by elevated triglyceride levels. The first diagnosis of familial hypertriglyeeridemia was based on elevated plasma triglyeeride levels of proband, at least two first-degree relatives with hypertriglyeeridemia, excluding secondary hypertriglyceridemia. With the deepening of the research, diagnostic criteria is also growing, and total apolipoprotein B level is added to the latest standards. The confirmed diagnosis of FHTG needs identification from other primary and secondary hypertriglyeeridemia. Here is to make a review of the clinical diagnostic criteria and differential diagnosis of FHTG.

关 键 词：家族性高三酰甘油血症 诊断标准 鉴别诊断 

分 类 号：R589.2[医药卫生—内分泌]