ICD-11 编码查询_国际疾病分类第 11 版中文版_在线疾病编码检索工具
LA75.5

先天性肺叶性肺气肿

Congenital lobar emphysema

上级条目
LA75 肺结构发育异常
层级
5 级

定义

先天性大叶性肺气肿是一种发育性肺异常,其特征是受累肺叶过度扩张,导致邻近正常肺组织和纵隔受压和移位。在大多数情况下,症状出现在新生儿期或幼儿期。临床上,儿童出现呼吸窘迫症状,常伴下呼吸道感染,加重空气潴留,使患者出现症状。

Congenital lobar emphysema is a developmental lung anomaly characterised by over distension of the affected lobe and leading to compression and displacement of adjacent normal lung tissue and mediastinum. In the majority of cases, symptoms appear during the neonatal period or in early childhood. Clinically, children present with signs of respiratory distress, frequently occurring with a lower respiratory tract infection that aggravates air trapping and renders the patient symptomatic.

索引词 可用于检索该条目的同义词与别名

  • 先天性肺叶性肺气肿
  • 先天性大叶性肺气肿
  • 单侧先天性大叶性肺气肿
  • 双侧先天性大叶性肺气肿
英文词条(3)
  • Congenital lobar emphysema
  • Congenital lobar emphysema, unilateral
  • Congenital lobar emphysema, bilateral

后组配轴 Postcoordination

后组配是在主干编码之后追加的可选扩展轴(如侧别、具体解剖部位、严重程度),用于把「部位 + 侧别 + 病程」等细节一次表达完整。只有标注「必填」的轴在组合编码时必须给出,其余可留空。

  • 侧别laterality可选
  • 具体解剖部位specificAnatomy可选