巴德-吉亚利综合征误诊1例报道  

Misdiagnosis of Budd-Chiari syndrome:one case report

作　　者：魏玉珠[1] 陈嘉屿[1] 边向聪 王志宏[2] 杨永林[1] 洪金鹏[1] 王彪猛[1] 

机构地区：[1]兰州军区兰州总医院消化内科,甘肃兰州730050 [2]兰州军区兰州总医院介入疼痛科,甘肃兰州730050

出　　处：《胃肠病学和肝病学杂志》2016年第12期1376-1378,共3页Chinese Journal of Gastroenterology and Hepatology

摘　　要：巴德-吉亚利综合征(Budd-Chiari syndrome,BCS)简称布加综合征,属临床少见病,多因其引起的门脉高压症而易误诊为隐源性肝硬化。临床典型表现为肝大、门-体侧支循环和腹水三联征。现将兰州军区兰州总医院近期收治1例初诊时误诊为隐源性肝硬化失代偿期的BCS患者报道如下,通过对该病例诊治过程的分析讨论,以期提高临床医师对该病的重视,减少临床误诊、误治。Budd-Chiari syndrome （BCS） or syndrome de Budd-Chiari is a rare clinical disease, more because of the cause of portal hypertension, it is easily misdiagnosed as cryptogenic cirrhosis. Typical clinical manifestations are big liver, portac-aval collateral circulation and ascites. Now, one case of BCS was reported which misdiagnosed as crypto- genic decompensated cirrhosis. Based on the analysis of the process of diagnosis and treatment of the case discussion, in order to improve the clinical doctor＇ s emphasis on the disease, reduce misdiagnosis and mistherapy.

关 键 词：巴德-吉亚利综合征 误诊分析 

分 类 号：R575[医药卫生—消化系统]