Tsuprun Vladimir, Schleiss Mark R, Cureoglu Sebahattin
Department of Otolaryngology-Head and Neck Surgery, University of Minnesota, Minneapolis, MN, USA.
Division of Pediatric Infectious Disease and Immunology, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
Ann Clin Pathol. 2022;9(1). Epub 2022 Aug 29.
Human temporal bones of newborns with congenital cytomegalovirus (cCMV) infection can be characterized by diverse cochlear and vestibular histopathologies associated with the variability in sensorineural hearing loss (SNHL) and vestibular dysfunction in these newborns.
Only a small number of studies on the cochlear and vestibular pathologies in human temporal bones with cCMV infection have been previously reported.
Cochleovestibular histopathologies were evaluated in 4 temporal bones from 3 infants with cCMV infection by light microscopy.
In one available temporal bone of the infant in Case 1, no cytomegalic cells were found. Large areas of cellular and non-cellular structures were observed in the scala tympani of the perilymphatic space; however, there was no obvious loss of cochlear or vestibular hair cells. In Case 2, cytomegalic cells, a loss of vestibular hair cells, and a loss of nerve fibers were observed only in the area of dark cells in the vestibular labyrinth of the left temporal bone. No cytomegalic cells were found in the right temporal bone of the same infant; however, there was a loss of outer hair cells in the organ of Corti and hypervascularity in the stria vascularis. The one available temporal bone of the infant in Case 3 showed cytomegalic cells and a loss of hair cells in both cochlear and vestibular parts of the inner ear.
Human temporal bones of newborns with cCMV demonstrate diverse cochleovestibular histopathologies. This diversity is consistent with the variable SNHL and vestibular dysfunction reported in infected newborns.
先天性巨细胞病毒(cCMV)感染的新生儿颞骨具有多种耳蜗和前庭组织病理学特征,这些特征与这些新生儿感音神经性听力损失(SNHL)和前庭功能障碍的变异性相关。
先前仅有少数关于cCMV感染的人类颞骨耳蜗和前庭病理学的研究报道。
通过光学显微镜对3例cCMV感染婴儿的4块颞骨的耳蜗前庭组织病理学进行评估。
在病例1婴儿的一块可用颞骨中,未发现巨细胞。在外淋巴间隙的鼓阶中观察到大面积的细胞和非细胞结构;然而,耳蜗或前庭毛细胞没有明显损失。在病例2中,仅在左侧颞骨前庭迷路的暗细胞区域观察到巨细胞、前庭毛细胞损失和神经纤维损失。在同一婴儿的右侧颞骨中未发现巨细胞;然而,柯蒂氏器中外毛细胞损失,血管纹血管增多。病例3婴儿的一块可用颞骨显示内耳的耳蜗和前庭部分均有巨细胞和毛细胞损失。
cCMV感染的新生儿颞骨表现出多种耳蜗前庭组织病理学特征。这种多样性与感染新生儿中报道的SNHL和前庭功能障碍的变异性一致。