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机构地区:[1]南方医科大学金陵医院(南京军区南京总医院)心胸外科,南京医学硕士研究生210002
出 处:《医学研究生学报》2015年第5期495-497,共3页Journal of Medical Postgraduates
基 金:国家自然科学基金(81172032)
摘 要:目的:肺隔离征是一种先天性肺发育畸形,该病发病率低、误诊率较高。文中结合肺隔离征患者临床资料,对该病的诊断与治疗进行总结分析。方法回顾性分析南京军区南京总医院心胸外科2009年9月至2014年9月收治的18例肺隔离征患者临床资料,其中男8例、女10例,年龄20~68岁,平均(42.37±14.63)岁。所有患者均行影像学检查,主要表现为肿块影(n=11)及囊性改变(n=7);均采取双腔气管内插管静脉复合麻醉,并行手术切除。结果17例叶内型行病变肺叶切除术,另1例叶外型行肺局部隔离病变切除术。明确诊断14例、误诊3例、漏诊1例。18例患者经手术治疗全部康复出院,随访8~18个月,无失访。患者生存良好,未出现与手术相关的并发症。结论肺隔离征临床表现缺乏特异性,分类诊断相对困难,手术治疗为主,术后预后良好。[Abstract ] Objective Pulmonary sequestration (PS) is a congenital development malformation of the lungs .This study aimed to explore the diagnosis and surgical treatment of PS . Methods We retrospectively analyzed the clinical data on 18 PS pa-tients (8 males and 10 females, aged 20-68 [42.34 ±14.63] years) treated in our department from September 2009 to September 2014.Medical imaging manifested tumors in 11 cases and cystic lesion in the other 7.All the patients underwent surgical resection . Results The diseased pulmonary lobes were removed for the 17 cases of the intralobar type and local resection was performed for the 1 case of the extralobar type .Fourteen of the cases were confirmed to be PS , 3 misdiagnosed, and 1 case missed at diagnosis .The pa-tients were followed up for 8-18 months after treatment , all recovered without surgery-related complications . Conclusion Pulmona-ry sequestration is a rare congenital malformation of the lungs and the lack of specific clinical manifestations makes it easy to be misdi -agnosed.Surgery is the main strategy for its treatment .
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