先天性巨细胞病毒与肺动脉高压

IF 1.3 4区 医学 Q3 PEDIATRICS
Layah Alkoby-Meshulam, Jacob Amir, Daniel Lubin, Gil Klinger, Giora Guttesman, Samuel Zangen, Efraim Bilavsky
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引用次数: 0

摘要

关于先天性巨细胞病毒感染患儿肺部受累的描述很少。我们描述了三例先天性巨细胞病毒感染儿童持续性肺动脉高压的新病例,并回顾了自 1988 年以来文献中报道的其他七例病例。所有患儿均有感染症状,包括严重的中枢神经系统或内脏症状。发病率和死亡率都很高。在症状严重的先天性巨细胞病毒感染婴儿中,持续性肺动脉高压可能是一种罕见的并发症。对特发性难治性持续肺动脉高压病例进行先天性巨细胞病毒筛查非常重要。在进行抗病毒治疗的同时,应进行强化治疗,以治疗这种潜在的罕见肺部受累。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital cytomegalovirus and pulmonary hypertension

Lung involvement in children with congenital cytomegalovirus infection has been scarcely described. We describe three new cases of persistent pulmonary hypertension in children with congenital cytomegalovirus and review the other seven cases reported in the literature since 1988. All children had a symptomatic infection, including severe central nervous system or visceral findings. Morbidity and mortality were high. Persistent pulmonary hypertension may be a rare complication in severely symptomatic congenital cytomegalovirus infants. It is important to screen for congenital cytomegalovirus in cases of idiopathic refractory persistent pulmonary hypertension. Intensive treatment should be undertaken to treat this potentially rare lung involvement in combination with antiviral treatment.

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来源期刊
Congenital Anomalies
Congenital Anomalies PEDIATRICS-
自引率
0.00%
发文量
49
审稿时长
>12 weeks
期刊介绍: Congenital Anomalies is the official English language journal of the Japanese Teratology Society, and publishes original articles in laboratory as well as clinical research in all areas of abnormal development and related fields, from all over the world. Although contributions by members of the teratology societies affiliated with The International Federation of Teratology Societies are given priority, contributions from non-members are welcomed.
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