Brain MRI in infants exposed to the Zika virus, with one-year follow-up: expanding the phenotype.

Q3 Medicine
Radiologia Brasileira Pub Date : 2024-11-07 eCollection Date: 2024-01-01 DOI:10.1590/0100-3984.2024.0014
Teresa Cristina de Castro Ramos Sarmet Dos Santos, Mai-Lan Ho, Maria de Fatima Vasco Aragão, Renata Artimos de Oliveira Vianna, Alexandre Ribeiro Fernandes, Alair Augusto Sarmet Moreira Damas Dos Santos, Claudete Aparecida Araújo Cardoso
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引用次数: 0

Abstract

Objective: To analyze longitudinal changes between two brain magnetic resonance imaging (MRI) exams performed one year apart in symptomatic infants with congenital Zika syndrome (CZS) and normocephalic infants exposed to the Zika virus (ZIKV) prenatally.

Materials and methods: This was a prospective observational study. Infants born to women who tested positive for ZIKV on reverse transcription-quantitative polymerase chain reaction during pregnancy were classified into two groups: symptomatic infants with CZS and asymptomatic infants. All of the infants underwent brain MRI at presentation and after one year of follow-up. All MRI scans were evaluated independently by a pediatric radiologist and a pediatric neuroradiologist, and the infants underwent clinical monitoring by a pediatric neurologist.

Results: The sample included 36 infants exposed to ZIKV perinatally. Therefore, a total of 72 MRI scans were evaluated. Among the 36 infants included a diagnosis of CZS was made in 25 (69.4%), of whom 18 presented with a combination of classic findings (including reduced brain volume, subcortical calcifications, brainstem hypoplasia, malformations of the corpus callosum, malformations of cortical development, and ventriculomegaly), as well as atypical findings such as hyperintense foci in the white matter on T2-weighted sequences. Of those same 25 infants, seven presented with mild lesions. Of the 11 normocephalic patients, five (13.9%) had atypical findings such as hyperintense foci in the white matter on T2-weighted sequences and no other manifestations of CZS, although there was mild neurological involvement. Six (16.6%) of the 36 patients had completely normal MRI scans with no neurological changes. No disease progression was observed during follow-up.

Conclusion: In infants exposed to ZIKV perinatally, the frequency of classic and atypical findings on brain MRI seems to be associated with the neurological status. Brain MRI is an important diagnostic tool in the evaluation and monitoring of patients with congenital infection, because intracranial changes other than microcephaly can occur.

暴露于寨卡病毒的婴儿脑磁共振成像及一年随访:扩展表型。
目的分析先天性寨卡综合征(CZS)无症状婴儿和产前暴露于寨卡病毒(ZIKV)的正常颅脑婴儿两次脑磁共振成像(MRI)检查之间相隔一年的纵向变化:这是一项前瞻性观察研究。将妊娠期反转录定量聚合酶链反应检测出 ZIKV 阳性的妇女所生的婴儿分为两组:有症状的 CZS 婴儿和无症状婴儿。所有婴儿在发病时和随访一年后都接受了脑部核磁共振成像检查。所有核磁共振扫描均由一名儿科放射科医生和一名儿科神经放射科医生独立评估,并由一名儿科神经科医生对婴儿进行临床监测:结果:样本包括36名在围产期感染ZIKV的婴儿。因此,共对 72 例磁共振成像扫描进行了评估。在这36名婴儿中,有25名婴儿(69.4%)被诊断为CZS,其中18名婴儿合并有典型的检查结果(包括脑容量减少、皮质下钙化、脑干发育不良、胼胝体畸形、皮质发育畸形和脑室肥大)以及非典型检查结果,如T2加权序列上的白质高强灶。在这 25 名婴儿中,有 7 名出现轻度病变。在11名正常头型患者中,有5名(13.9%)在T2加权序列上发现了白质中的高张力灶等非典型表现,但没有其他CZS表现,只是有轻微的神经系统受累。36 名患者中有 6 人(16.6%)的磁共振成像扫描结果完全正常,没有神经系统病变。随访期间未发现疾病进展:结论:在围产期感染 ZIKV 的婴儿中,脑磁共振成像典型和非典型结果的频率似乎与神经系统状况有关。脑磁共振成像是评估和监测先天性感染患者的重要诊断工具,因为除了小头畸形外,还可能出现其他颅内病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Radiologia Brasileira
Radiologia Brasileira Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
2.60
自引率
0.00%
发文量
75
审稿时长
28 weeks
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