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Prenatal Diagnosis and Pathology of Laryngeal Atresia in Congenital High Airway Obstruction Syndrome

机译:先天性高气道阻塞综合征的喉闭锁的产前诊断和病理

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摘要

Congenital high airway obstruction syndrome is a rare but life-threatening condition. Therefore, prenatal diagnosis is important. The obstruction can be due to laryngeal/tracheal atresia or external compression. While a differential diagnosis with congenital cystic adenomatoid malformation (CCAM) type III may be difficult, it is still possible with ultrasonography. In this study, we report a case of bilateral echogenic lungs with hydrops fetalis. After the prenatal diagnosis of laryngeal atresia, the couple opted to have an elective termination of pregnancy performed at 20 weeks of gestation. The diagnosis was confirmed by a complete pathological examination.
机译:先天性高气道阻塞综合征是一种罕见但危及生命的疾病。因此,产前诊断很重要。阻塞可归因于喉/气管闭锁或外部压迫。虽然先天性囊性腺瘤样畸形(CCAM)III型的鉴别诊断可能很困难,但超声检查仍可能。在这项研究中,我们报告了胎儿水肿的双侧回声肺病例。在产前诊断出喉咙闭锁后,这对夫妇选择在妊娠20周时选择性终止妊娠。完整的病理检查证实了诊断。

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