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先天性巨细胞病毒感染的人胎儿内耳受累。

Human fetal inner ear involvement in congenital cytomegalovirus infection.

机构信息

Operative Unit of Clinical Microbiology, St, Orsola-Malpighi General Hospital, University of Bologna, Via Massarenti 9, 40138, Bologna, Italy.

出版信息

Acta Neuropathol Commun. 2013 Oct 2;1:63. doi: 10.1186/2051-5960-1-63.

DOI:10.1186/2051-5960-1-63
PMID:24252374
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3893406/
Abstract

BACKGROUND

Congenital cytomegalovirus (CMV) infection is a leading cause of sensorineural hearing loss (SNHL). The mechanisms of pathogenesis of CMV-related SNHL are still unclear. The aim is to study congenital CMV-related damage in the fetal inner ear, in order to better understand the underlying pathophysiology behind CMV-SNHL.

RESULTS

We studied inner ears and brains of 20 human fetuses, all at 21 week gestational age, with a high viral load in the amniotic fluid, with and without ultrasound (US) brain abnormalities. We evaluated histological brain damage, inner ear infection, local inflammatory response and tissue viral load.Immunohistochemistry revealed that CMV was positive in 14/20 brains (70%) and in the inner ears of 9/20 fetuses (45%). In the cases with inner ear infection, the marginal cell layer of the stria vascularis was always infected, followed by infection in the Reissner's membrane. The highest tissue viral load was observed in the inner ear with infected Organ of Corti. Vestibular labyrinth showed CMV infection of sensory cells in the utricle and in the crista ampullaris.US cerebral anomalies were detected in 6 cases, and in all those cases, the inner ear was always involved. In the other 14 cases with normal brain scan, histological brain damage was present in 8 fetuses and 3 of them presented inner ear infection.

CONCLUSIONS

CMV-infection of the marginal cell layer of the stria vascularis may alter potassium and ion circulation, dissipating the endocochlear potential with consequent SNHL. Although abnormal cerebral US is highly predictive of brain and inner ear damage, normal US findings cannot exclude them either.

摘要

背景

先天性巨细胞病毒(CMV)感染是感音神经性听力损失(SNHL)的主要原因。CMV 相关 SNHL 的发病机制尚不清楚。目的是研究胎儿内耳中与先天性 CMV 相关的损伤,以便更好地了解 CMV-SNHL 背后的潜在病理生理学。

结果

我们研究了 20 个人类胎儿的内耳和大脑,所有胎儿均在 21 孕周时羊水病毒载量高,伴有或不伴有超声(US)脑异常。我们评估了组织学脑损伤、内耳感染、局部炎症反应和组织病毒载量。免疫组织化学显示,20 个脑中有 14 个(70%)和 9 个胎儿的内耳(45%)呈 CMV 阳性。在内耳感染的病例中,血管纹的边缘细胞层总是被感染,其次是 Reissner 膜被感染。在内耳感染的病例中,感染的耳蜗器官中的组织病毒载量最高。前庭迷路显示耳石和壶腹嵴的感觉细胞感染 CMV。在 6 例 US 脑异常的病例中,内耳总是受累。在另外 14 例大脑扫描正常的病例中,8 例胎儿存在组织学脑损伤,其中 3 例存在内耳感染。

结论

血管纹边缘细胞层的 CMV 感染可能会改变钾和离子循环,使内淋巴电位耗散,从而导致 SNHL。尽管异常的大脑 US 高度预测脑和内耳损伤,但正常的 US 结果也不能排除这些损伤。

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