Prenatal diagnosis of primary right pulmonary agenesis: a case report
10.3760/cma.j.cn113903-20200213-00097
- VernacularTitle:产前诊断原发性右侧肺缺如且生后健康存活一例
- Author:
Zonghui FENG
;
Gang YU
;
Yan CHEN
;
Fengmei YI
;
Min LI
;
Shumin JIANG
- From:
Chinese Journal of Perinatal Medicine
2021;24(1):61-64
- CountryChina
- Language:Chinese
-
Abstract:
We report the prenatal diagnosis and treatment of a case of primary right pulmonary deficiency. A routine ultrasound examination at 23 +6 weeks of gestation found an absent right lung, enlarged left lung, and dextroposition of the heart in a female fetus. Karyotype and chromosome microarray analysis of the amniotic fluid was normal. After multidisciplinary consultation, the pregnant woman chose to continue the pregnancy and had a normal delivery at 39 +2 gestational weeks. Apgar scores were ten at both 1 min and 5 min after birth, with no abnormal appearance of the baby, or signs of thoracic collapse other than no obvious respiratory sounds in the right lung. Both postnatal chest X-ray and CT scan indicated an undeveloped right lung. Cardiac ultrasonography revealed the absence of the right pulmonary artery and vein. The patient's breathing was stable during hospitalization and she was discharged eight days after birth. The infant was followed up at five months, and the growth and development were comparable to children of the same age.