Tegllund L
Arhus Kommunehospital, pediatrisk afdeling.
Ugeskr Laeger. 1990 Mar 19;152(12):826-7.
Congenital cystic adenomatoid malformation (MCAM) is a rare disease which commences as a rule in the neonatal period with respiratory distress. The diagnosis is established radiologically but may also be established prenatally by ultrasound scanning. Treatment is surgical. Two cases of MCAM are described. One was a boy aged 5 1/2 months with failure to thrive and the other a 28 week foetus with hydrops foetalis.
先天性囊性腺瘤样畸形（MCAM）是一种罕见疾病，通常在新生儿期开始出现呼吸窘迫症状。诊断通过放射学方法确立，但也可在产前通过超声扫描确立。治疗方法为手术治疗。本文描述了两例MCAM病例。一例是一名5个半月大的男孩，发育不良；另一例是一名患有胎儿水肿的28周胎儿。
