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
LB30.9

多囊肾发育不良

Multicystic renal dysplasia

上级条目
LB30 肾结构发育异常
层级
5 级

定义

多囊性肾发育不良(Multicystic renal dysplasia),或称多囊性发育不良肾(MCDK),是一种先天性疾病,指胎儿期肾脏未能正常发育,而是形成了充满液体的囊肿,而非正常的肾组织。最常影响单侧肾脏,而另一侧健康的肾脏通常可以代偿其功能,且多通过产前超声检查发现。双侧MCDK(影响双肾)是一种非常严重的情况,肾衰竭风险高,通常难以长期存活。

Multicystic renal dysplasia, or multicystic dysplastic kidney (MCDK), is a congenital condition where a kidney fails to develop properly in the womb, becoming a non-functional collection of fluid-filled cysts instead of normal kidney tissue. It most often affects a single kidney, allowing the other healthy kidney to compensate for its function, and is usually discovered via prenatal ultrasound. Bilateral MCDK, affecting both kidneys, is a very serious condition with a high risk of kidney failure and is often incompatible with long-term survival.

索引词 可用于检索该条目的同义词与别名

  • 多囊肾发育不良
  • MCDK - [多囊性肾发育不良]
  • 发育性多囊肾
  • 多囊性肾发育不良
  • 多发性先天性肾囊肿
  • 单侧多囊性肾发育不良
  • 单侧多囊性肾发育不良
  • 双侧多囊性肾发育不良
英文词条(8)
  • Multicystic renal dysplasia
  • MCDK - [multicystic dysplastic kidney]
  • developmental multicystic kidney
  • multicystic dysplastic kidney
  • multiple congenital cysts of kidney
  • Multicystic renal dysplasia, unilateral
  • Unilateral multicystic dysplastic kidney
  • Multicystic renal dysplasia, 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