Ultrasonographic diagnosis and clinical prognosis of fetal congenital cystic adenomatoid malformation of the lung
- VernacularTitle:胎儿先天性肺腺瘤样囊肿的超声诊断与临床预后
- Author:
Hongmei CHANG
;
Lingling SUN
;
Xuedong DENG
;
Hong LIANG
;
Yiping ZHAO
;
Feng FAN
- Publication Type:Journal Article
- Keywords:
Fetus;
Congenital cystic adenomatoid malformation of the lung;
Ultrasonogrphy,prenatal
- From:
Chinese Journal of Medical Imaging Technology
2010;26(2):313-315
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the diagnostic value of ultrasonography of fetal congenital cystic adenomatoid malformation of the lung (CCAM), and to predict the prognosis according to ultrasonographic findings. Methods The chest of 19 fetus with CCAM was multi-sectionally scanned with two-dimensional ultrasonography. The position, appearance and size of mass were observed, and complications were continuously followed. Results CCAM was pathologically confirmed in 13 fetus after induced abortion. One neonatal died, while CCAM in other 5 fetus disappeared before 36 weeks. The mass of typeⅠCCAM became smaller and smaller, and eventually disappeared. The echo-free spaces in typeⅡbecame smaller and fewer, and the strong echo weakened to the same level as normal lung. For type Ⅲ, the echo of solid mass weakened to the same level as normal lung, or transformed to typeⅡ gradually, and finally recovered to normal echo of lung as the gestational age increased. During follow up, there were 10 fetus (10/19, 52.63%) that lung adenoma cyst increased with the gestational age increased, and the heart, mediastinal shifted, pleural effusion, and (or) fetal edema were observed. Conclusion Ultrasound examination is a reliable method for the diagnosis of CCAM, and enable to predict the prognosis of the affected fetuses. If heart and mediustinum displacement, pleural effusion, hydrops fetal or other abnormalities exist, it's necessary to terminate the pregnancy.
