妇女细小病毒感染

Patricia A Devine MD
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引用次数: 3

摘要

细小病毒B19是儿童感染性渗漏性红斑的病原体。传染性红斑可零星发生,或作为社区暴发的一部分。疫情通常发生在冬末和早春期间的小学。年龄增长与既往B19感染流行率增加有关。主要传播方式是通过呼吸道分泌物和手口接触。易感孕妇感染细小病毒B19的风险与她与儿童的接触程度和接触环境密切相关。血清转换的最大危险因素是有一个6至7岁的孩子。成人最常见的临床表现是对称周围性多关节病。母体感染的诊断通常由母体血清学来确定。如果患者在怀孕期间感染细小病毒B19,胎儿感染的风险可高达33%。胎儿感染的机制是母体病毒血症伴细小病毒B19经胎盘传代。受感染的胎儿有发生再生障碍性贫血、心力衰竭和水肿的危险。当母体感染发生在妊娠10-20周之间时,胎儿死亡最常见,死亡率可高达10%。近期有细小病毒B19感染血清学证据的孕妇应每周进行超声检查,寻找积液的迹象。如果出现积液,应考虑髓鞘穿刺术。间接证据支持在有严重胎儿贫血和水肿的特定病例中进行宫内输血。先天性细小病毒感染的长期后遗症是罕见的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Parvovirusinfection in women

Parvovirus B19 is the causative agent of the childhood exanthem erythema infectiosum. Erythema infectiosum can occur sporadically, or as part of community outbreaks. Outbreaks typically occur in elementary schools during the late winter and early spring. Increasing age is associated with an increasing prevalence of prior B19 infection. The primary mode of transmission is through respiratory secretions and hand-to-mouth contact. A susceptible pregnant woman’s risk of parvovirus B19 infection is closely associated with her level of contact with children and the environment in which the exposure takes place. The greatest risk factor for seroconversion is having a child aged 6 to 7 years. The most common clinical presentation in adults is symmetrical peripheral polyarthropathy. Diagnosis of maternal infection is usually established by maternal serology. If a patient contracts parvovirus B19 infection during pregnancy, the risk of fetal infection can be as high as 33%. The mechanism for fetal infection is maternal viremia with transplacental passage of parvovirus B19. The infected fetus is at risk for developing aplastic anemia, heart failure, and hydrops. Fetal death occurs most frequently when maternal infection takes place between 10–20 weeks’ gestation, and may be as high as 10%. Pregnant women with serologic evidence of recent parvovirus B19 infection should be followed with weekly ultrasound examinations, looking for signs of hydrops. If hydrops develops, consideration should be given to cordocentesis. Circumstantial evidence supports performing intrauterine transfusion in selected cases with severe fetal anemia and hydrops. Long-term sequelae of congenital parvovirus infection are rare.

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