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巨细胞病毒胎儿病中的胼胝体损伤:一项神经超声研究。

Callosal Injuries in Cytomegalovirus Fetopathy: A Neurosonographic Study.

作者信息

Krajden Haratz Karina, Malinger Gustavo, Miremberg Hadas, Hartoov Joseph, Wolman Igal, Jaffa Ariel, Busilov Michael, Birnbaum Roee

机构信息

Division of Ultrasound in ObGyn at Lis Maternity and Women's Hospital, Tel Aviv Medical Center, Tel Aviv, Israel,

Affiliated to the Tel Aviv University, Tel Aviv, Israel,

出版信息

Fetal Diagn Ther. 2025;52(3):243-253. doi: 10.1159/000541794. Epub 2024 Oct 4.

Abstract

INTRODUCTION

Among the fetal brain anomalies described in cases of congenital infection, callosal insults are rarely cited in medical literature. The aim of this study was to describe the rate and pattern of callosal injury in cytomegalovirus (CMV) fetopathy.

METHODS

This retrospective study included fetuses with confirmed CMV-PCR, assessed in a single center. Demographic data including maternal seroconversion info were collected. Dedicated US including neurosonography was performed, with high frequency probes, using TV route whenever feasible. Fetal brain biometry including callosal length and the corpus callosum (CC)/OFD ratio was performed. Length below the 5th centile or morphological abnormalities were considered abnormal. Brain and body morphology were thoroughly assessed, and any abnormal finding reported.

RESULTS

Seventy-two patients were included in our cohort. In 76% infection occurred in the 1st T or periconceptional. In 12 patients, the exact time of infection was inconclusive, including two cases of secondary infection. In 34.7%, a callosal anomaly was observed and it was never isolated. CNS abnormalities included: periventricular hyperechogenicity (PVHE) 55.5%, calcifications 52%, ventriculomegaly 33%, periventricular pseudocysts 31.4%, occipital cysts 22.2%, echogenic ganglionic eminence 30.5%, lentostriatal vasculopathy 26.4%, sulcation abnormalities 22.2%, cerebellar findings 18% and HC below -2 SD 18%. In 19 cases, the CC was short with calcifications in four. In one case, the insult was severe and in another the CC was absent. The most common association with CC insult was PVHE (56%) and calcifications (52%).

CONCLUSION

Although not referred as a classic brain structure affected by CMV infection, the CC was injured in one-third of our patients, including cases of late infection. The mechanism of disease and the prenatal patterns of callosal involvement in these cases appear to be different from the postnatal patterns and are not reversible. The presence of a callosal injury would imply a worse prognosis and significant increment to the risk of neurodevelopmental impairment.

摘要

引言

在先天性感染病例中所描述的胎儿脑异常中,胼胝体损伤在医学文献中很少被提及。本研究的目的是描述巨细胞病毒(CMV)胎儿病中胼胝体损伤的发生率和模式。

方法

这项回顾性研究纳入了在单一中心评估的经CMV-PCR确诊的胎儿。收集了包括母亲血清转化信息在内的人口统计学数据。使用高频探头进行专门的超声检查,包括神经超声检查,只要可行就采用经阴道途径。进行了胎儿脑生物测量,包括胼胝体长度和胼胝体(CC)/枕额径(OFD)比值。长度低于第5百分位数或形态异常被视为异常。对脑和身体形态进行了全面评估,并报告了任何异常发现。

结果

我们的队列纳入了72例患者。76%的感染发生在妊娠第1期或受孕前后。12例患者的确切感染时间不确定,包括2例继发感染。34.7%的患者观察到胼胝体异常,且从未单独出现。中枢神经系统异常包括:脑室周围高回声(PVHE)55.5%、钙化52%、脑室扩大33%、脑室周围假性囊肿31.4%、枕叶囊肿22.2%、神经节隆起回声增强30.5%、豆纹状血管病变26.4%、脑沟异常22.2%、小脑异常18%和头围低于-2标准差18%。19例患者的胼胝体较短,4例有钙化。1例损伤严重,另1例无胼胝体。与胼胝体损伤最常见的关联是PVHE(56%)和钙化(52%)。

结论

尽管胼胝体未被视为受CMV感染影响的典型脑结构,但在我们三分之一的患者中受到了损伤,包括晚期感染病例。这些病例中疾病的机制和胼胝体受累的产前模式似乎与产后模式不同且不可逆转。存在胼胝体损伤意味着预后更差,神经发育障碍风险显著增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc20/12129428/d6feb697ff63/fdt-2025-0052-0003-541794_F01.jpg

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