临床儿科杂志 ›› 2018, Vol. 36 ›› Issue (12): 932-.doi: 10.3969/j.issn.1000-3606.2018.12.012

• 综合报道 • 上一篇    下一篇

儿童先天性单侧肺动脉发育不良或缺如临床分析#br#

肖云彬 1,2, 曾云红 1,2, 王野峰 1, 杨舟 1, 左超 1, 陈智 1,2   

  1. 1.湖南省儿童医院心血管内科(湖南长沙 410007);2.南华大学儿科学院(湖南长沙 410007)
  • 收稿日期:2018-12-15 出版日期:2018-12-15 发布日期:2018-12-15
  • 通讯作者: 陈智 E-mail:eychenzhi@163.com

Clinical manifestation of pediatric patients with congenital unilateral agenesis or absence of pulmonal artery

XIAO Yunbin1,2, ZENG Yunhong2, WANG Yefeng1, YANG Zhou1, ZUO Chao1, CHEN Zhi1,2   

  1. 1. Department of Cardiology, Hunan Children's Hospital, Changsha 410007, Hunan, China; 2. Academy of Pediatrics, University of South China, Changsha 410007, Hunan, China
  • Received:2018-12-15 Online:2018-12-15 Published:2018-12-15

摘要: 目的 探讨儿童先天性单侧肺动脉发育不良或缺如的临床表现及诊断。方法 回顾分析5例诊断为先天性 单侧肺动脉发育不良或缺如患儿的临床资料。结果 男3例、女2例,初诊年龄7个月~13岁。其中4例为先天性单侧肺动 脉发育不良, 1例为单侧肺动脉缺如。主要临床表现为反复肺部感染、咯血、肺动脉高压。 X线平片示患侧肺纹理稀疏,健 侧肺血增多,纵隔向健侧移位。超声心动图示不同程度肺动脉高压及合并的心内畸形。胸部CT和心导管造影可良好显示 肺血管的走形和发育。结论 儿童先天性单侧肺动脉发育不良或缺如主要临床表现为反复肺部感染、咯血、肺动脉高压。 X线平片、超声心动图可提供早期诊断线索。胸部增强CT扫描、心导管造影可明确诊断。

Abstract:  Objective The objectives of this study are to investigate the clinical characteristics and improve the diagnosis of pediatric patients with congenital unilateral agenesis or absence of pulmonal artery. Methods Cases of pediatric patients with congenital unilateral agenesis or absence of a pulmonal arterywho had been diagnosed at our hospital from 2008 to 2018 were analyzed. Results In all, five patients (3 male; age range, 0.58-13 years) with congenital unilateral agenesis or absence of pulmonal artery were diagnosed and treated in our institution.The most common clinical presentation are recurrent pulmonary infections, hemoptysis and pulmonary artery hypertension. The chest X-ray was indicative in the regular clinical examinations though it was of no value in the diagnosis. Echocardiography could demonstrate associated intracardiac defects and pulmonary artery hypertension. The catheterization and chest computed tomography scan could show distinctly the conditions of pulmonary arteries. Conclusion The common clinical manifestation of pediatric patients with congenital unilateral agenesis or absence of pulmonal artery arerecurrent pulmonary infections, pulmonary hypertension and hemoptysis. The chest X-ray and echocardiography indicate diagnosis, contrast enhanced chest computed tomography or angiography could confirm diagnosis.