LB12.1
食管闭锁
Atresia of oesophagus
- 上级条目
- LB12 食管结构发育异常
- 层级
- 5 级
定义
食道闭锁包括一组先天性异常，食道连续性中断，有或无与气管持续交通。86%的病例有远端气管食管瘘，7%的病例没有瘘管连接，而4%的病例有无闭锁的气管食管瘘。其余病例为OA伴近端或近端和远端气管食管瘘患者。
Oesophageal atresia encompasses a group of congenital anomalies with an interruption in the continuity of the oesophagus, with or without persistent communication with the trachea. In 86% of cases there is a distal tracheoesophageal fistula, in 7% of cases there is no fistulous connection, while in 4% of cases there is a tracheoesophageal fistula without atresia. The remaining cases are made up of patients with OA with proximal, or both proximal and distal, tracheoesophageal fistula.
跨章引用 同一概念在其他章节另有编码
子条目 共 3 条
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。
- 具体解剖部位specificAnatomy可选