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儿童先天性巨细胞病毒感染后出现间歇性前庭症状:病例系列研究。

Episodic Vestibular Symptoms in Children With a Congenital Cytomegalovirus Infection: A Case Series.

机构信息

Department of Head and Skin.

Department of Rehabilitation Sciences, Ghent University.

出版信息

Otol Neurotol. 2019 Jul;40(6):e636-e642. doi: 10.1097/MAO.0000000000002244.

DOI:10.1097/MAO.0000000000002244
PMID:31135673
Abstract

OBJECTIVE

Congenital cytomegalovirus (cCMV) infection is the most common non-genetic cause of sensorineural hearing loss in children. Although cCMV-induced vestibular loss is demonstrated in several studies, the occurrence of vertigo has been described in only two cases to date. The aim of this paper is to discuss the underlying pathophysiology of recurrent vestibular symptoms in children with cCMV, based on five cases investigated in our center and an extensive research of the literature.

STUDY DESIGN

Retrospective case series.

SETTING

Tertiary referral center.

PATIENTS

This case series describes five pediatric cCMV-patients (three boys, two girls). Four of them were symptomatic at birth, one was asymptomatic. Three patients underwent cochlear implantation. The age of onset of the vestibular symptoms varied from 2;0 to 7;3 years of age.

INTERVENTION

None.

MAIN OUTCOME MEASURES

Details regarding the patient history and results of cranial imaging, audiological, vestibular, and neurological assessments were collected retrospectively.

RESULTS

The selected cases suffered from recurrent vestibular symptoms. All patients had delayed onset, fluctuating, and/or progressive hearing loss. In all cases, the attacks were accompanied with nausea and vomiting and occurred without clear-cut trigger. Migraine and epilepsy often were proposed as first diagnosis, although they could not be confirmed eventually. Four out of five patients were diagnosed with a peripheral vestibular deficit.

CONCLUSIONS

Diagnosis of vestibular symptoms in children with cCMV is complex, given the multiple morbidities than can occur. Peripheral vestibular causes should be considered in the diagnosis, as important vestibular deficits are demonstrated in this population.

摘要

目的

先天性巨细胞病毒(cCMV)感染是儿童感音神经性听力损失的最常见非遗传原因。尽管已有多项研究证明 cCMV 可引起前庭功能丧失,但迄今为止仅描述了两例眩晕发生病例。本文旨在基于我们中心调查的五例病例和广泛的文献研究,讨论儿童 cCMV 反复出现前庭症状的潜在病理生理学。

研究设计

回顾性病例系列。

设置

三级转诊中心。

患者

本病例系列描述了五例儿科 cCMV 患者(三男两女)。其中四人出生时出现症状,一人无症状。三名患者接受了耳蜗植入。前庭症状的发病年龄从 2 岁 0 个月到 7 岁 3 个月不等。

干预措施

无。

主要观察指标

回顾性收集患者病史和头颅影像学、听力学、前庭和神经学评估结果的详细信息。

结果

所选病例均患有复发性前庭症状。所有患者均有延迟发病、波动性和/或进行性听力损失。在所有病例中,发作时伴有恶心和呕吐,且无明确诱因。偏头痛和癫痫常被作为最初诊断提出,但最终无法得到证实。五例中有四例被诊断为外周前庭功能减退。

结论

由于可能发生多种合并症,因此 cCMV 患儿的前庭症状诊断较为复杂。应考虑外周前庭病因,因为该人群中存在重要的前庭功能减退。

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