Neonatal Department of Intensive Medicine Comenius University in Bratislava, National Institute of Children's Diseases, Bratislava, Slovak Republic.
Physiol Res. 2020 Dec 31;69(Suppl 4):S637-S647. doi: 10.33549/physiolres.934613.
Congenital lung masses (CLM) the rare group of causes of acute respiratory insufficiency (RI) in newborns include congenital airway pulmonary malformation (CAPM), congenital overinflation, bronchopulmonary sequestration, and bronchial atresia. The presenting group consists of 13 newborns who were admitted to the Neonatal Department of Intensive Medicine (NDIM) during January 1st 2015-December 31st 2019 (8 males, 5 females, 2 premature/11 term newborns, spontaneous delivery: 2, caesarean section: 11) with positive prenatal diagnosis of CAPM in all cases. In 2 cases prenatal intervention was performed (drainage of the amniotic fluid, attempt of thoracentesis). Signs of acute RI immediately after delivery were seen in 5 newborns. Postnatal echocardiographic investigation confirmed the presence of increased pulmonary pressure in 8 patients, no patient had congenital heart abnormality. A thorax x-ray was positive also in asymptomatic patients. Computed tomography in patients brought detailed information about the position, size and character of CAPM. Six patients underwent surgery. In 15.4 % right lungs were affected by cystic malformation and in 23 % left lungs were affected. A final diagnosis of CAPM was confirmed in 5 patients using histopathologic examination. Multidisciplinary cooperation during prenatal as well as postnatal period is necessary.
先天性肺肿块(CLM)是导致新生儿急性呼吸功能不全(RI)的罕见病因群,包括先天性气道肺畸形(CAPM)、先天性过度充气、肺隔离症和支气管闭锁。本研究组包括 13 名于 2015 年 1 月 1 日至 2019 年 12 月 31 日期间入住新生儿重症监护病房(NDIM)的新生儿(8 名男性,5 名女性,2 名早产儿/11 名足月儿,自然分娩:2 例,剖宫产:11 例),所有病例均有 CAPM 的产前阳性诊断。2 例进行了产前干预(羊水引流、胸腔穿刺尝试)。5 例新生儿在出生后立即出现急性 RI 征象。8 例患者的产后超声心动图检查证实存在肺动脉高压,无患者存在先天性心脏病异常。无症状患者的胸部 X 线也呈阳性。CT 检查为患者提供了关于 CAPM 的位置、大小和特征的详细信息。6 名患者接受了手术。囊性畸形累及右肺的比例为 15.4%,左肺的比例为 23%。5 名患者通过组织病理学检查最终确诊为 CAPM。产前和产后的多学科合作是必要的。