Kartagener综合征1例报告并文献复习  

Kartagener syndrome 1 case report and review of the literature

作　　者：王丽霞[1] 唐晓丽[1] 

机构地区：[1]新疆医科大学附属中医医院肺病二科,新疆乌鲁木齐830000

出　　处：《世界最新医学信息文摘》2017年第32期19-20,共2页World Latest Medicine Information Electronic Version

摘　　要：目的探讨Kartagener综合征的临床特点、诊断标准及治疗方法。方法报告Kartagener综合征1例,回顾该患者的临床资料,复习国内外文献,进行总结分析。结果患者女性,43岁,反复咳嗽、咳黄脓痰6年,伴咯血,CT提示双肺支扩合并感染、全内脏反位,双侧上颌窦炎,经抗感染对症治疗1周病情好转出院。结论 Kartagener综合征是一种罕见的常染色体隐性遗传病,以全内脏反位,支气管扩张,副鼻窦炎三联征为诊断标准,治疗以对症治疗为主。Objective to explore the clinical features, diagnostic criteria and treatment methods of Kartagener syndrome.Methods the clinical data of Kartagener syndrome were reviewed, reviewed and reviewed in the literature.As a result, patients were female, 43, repeatedly cough, yellow purulent sputum for six years, with hemoptysis, CT prompted both lungs enlarge co-infection, completely splanchnic trans, bilateral maxillary sinusitis, the resistance to infection, symptomatic treatment improved hospital 1 week.Conclusion Kartagener syndrome is a rare autosomal recessive hereditary disease, trans in the gut, bronchiectasis, deputy nose views for diagnostic criteria, treatment is given priority to with symptomatic treatment.

关 键 词：KARTAGENER综合征 诊断 治疗 

分 类 号：R256.1[医药卫生—中医内科学]