Chinese Journal of Practical Pediatrics ›› 2022, Vol. 37 ›› Issue (4): 269-272.DOI: 10.19538/j.ek2022040607

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Genetic diagnosis of interstitial lung disease in children

  

  1. Department of Pulmonology,Children’s Hospital,Zhejiang University School of Medicine,National Clinical Research Center for Child Health,Hangzhou  310052,China
  • Online:2022-04-06 Published:2022-05-23

儿童间质性肺病的遗传学诊断

  

  1. 浙江大学医学院附属儿童医院呼吸内科  国家儿童健康与疾病临床医学研究中心,浙江  杭州  310052
  • 通讯作者: 唐兰芳,电子信箱:6195007@zju.edu.cn

Abstract: Child interstitial lung disease(chILD)is a group of rare,complicated and highly heterogeneous diseases,which are mainly characterized by diffuse lung infiltration,restrictive ventilation and ventilatory dysfunction.The diagnosis of chILD requires comprehensive analysis of age,clinical manifestations,chest high-resolution CT(HRCT),bronchoscopy and genetic analysis;especially,in the current rapid development of genetic analysis,bronchoscopy,thoracoscopiy and thoracotomic lung biopsy are no longer the main diagnostic methods.This elaborates on the genetic diagnosis of chILD.

Key words: interstitial lung disease, high-resolution CT of the chest, bronchoscopy, genetic analysis, child

摘要: 儿童间质性肺病(chILD)是一组少见、分类复杂、高度异质性疾病,其特点主要为肺弥漫性浸润、限制性通气和换气功能障碍。儿童间质性肺病的诊断需要结合年龄、临床表现、胸部高分辨率计算机断层扫描(HRCT)、支气管镜和遗传学检测综合分析得出,尤其是在遗传学检测迅猛发展的当下,支气管镜、胸腔镜、开胸肺组织活检将不再作为其主要诊断手段。文章就儿童间质性肺病的遗传学诊断进行详细阐述。

关键词: 间质性肺病, 胸部高分辨率CT, 支气管镜, 遗传学检测, 儿童