Meizner I, Sherizly I, Mashiach R, Shalev J, Kedron D, Ben-Rafael Z
Department of Obstetrics and Gynecology, Rabin Medical Center, Petah-Tikva 49100, Israel.
J Clin Ultrasound. 2000 Oct;28(8):435-8. doi: 10.1002/1097-0096(200010)28:8<435::aid-jcu10>3.0.co;2-7.
Congenital laryngeal atresia is an extremely rare anomaly that in most cases is incompatible with life. About 50% of cases involve other major malformations. Prenatal sonographic diagnosis of this condition has been described only 6 times. We present a case in which prenatal sonographic examination at 21 weeks' menstrual age revealed enlarged, hyperechoic lungs, dilated upper airways, ascites, and a single umbilical artery. To our knowledge, this is the first reported case of the prenatal diagnosis of laryngeal atresia in association with a single umbilical artery.
先天性喉闭锁是一种极其罕见的畸形,在大多数情况下与生命不相容。约50%的病例伴有其他主要畸形。关于这种情况的产前超声诊断仅报道过6次。我们报告一例,在月经龄21周时进行的产前超声检查显示肺增大、高回声、上呼吸道扩张、腹水和单脐动脉。据我们所知,这是第一例报道的产前诊断喉闭锁合并单脐动脉的病例。