Gianolio Laura, Fumagalli Mara, Manfredini Valeria, Mannarino Savina, Giacomet Vania, Zuccotti Gian Vincenzo
Department of Pediatric Infectious Diseases, Luigi Sacco University Hospital, Milano, Italy.
University of Milan, Milano, Italy.
J Matern Fetal Neonatal Med. 2022 Dec;35(25):6558-6560. doi: 10.1080/14767058.2021.1918086. Epub 2021 Apr 28.
While other viral infections occurring in early pregnancy are known to be associated with fetal cardiac malformations, little is known about CMV and its causative role. Only a few case repots have been described reporting a correlation between congenital CMV infection and cardiac defects. We report the case of a 7-day-old neonate who was referred to our Pediatric Infectivology Department for maternal cytomegalovirus (CMV) seroconversion during the first trimester of pregnancy and confirmed congenital infection. At first evaluation, the baby presented with a cardiac murmur and signs of acute heart failure, along with jaundice and hypotonia. At cardiac ultrasound, a perimembranous doubly-committed ventricular septal defect and a reduced aortic isthmus diameter were revealed. Despite further large-scale prospective studies are needed to confirm or rule out this association, CMV DNA urine detection might be worth to be considered as part of the diagnostic process in neonates with isolated heart defects.
虽然已知妊娠早期发生的其他病毒感染与胎儿心脏畸形有关,但对于巨细胞病毒(CMV)及其致病作用却知之甚少。仅有少数病例报告描述了先天性CMV感染与心脏缺陷之间的相关性。我们报告了一例7日龄新生儿的病例,该新生儿因母亲在妊娠早期巨细胞病毒血清学转换并确诊为先天性感染,被转诊至我们的儿科感染病科。初次评估时,婴儿出现心脏杂音和急性心力衰竭体征,伴有黄疸和肌张力减退。心脏超声检查发现膜周部双干下型室间隔缺损和主动脉峡部直径减小。尽管需要进一步的大规模前瞻性研究来证实或排除这种关联,但CMV DNA尿液检测可能值得作为孤立性心脏缺陷新生儿诊断过程的一部分加以考虑。