Iino Y, Komiya T, Fujii T, Nakamoto Y, Koyama S, Suzuki J I, Toriyama M
Department of Otolaryngology, Teikyo University School of Medicine, Tokyo. Japan.
Ear Nose Throat J. 1998 Aug;77(8):662-6, 668.
The temporal bones of two patients with profound bilateral deafness from infancy were studied immunohistochemically, using a neurofilament protein antibody to detect the cochlear neuronal elements. One patient exhibited Mondini dysplasia of the inner ear, with the organ of Corti almost completely deteriorated. The other patient is the first reported case involving complete aplasia of the organ of Corti in all turns. In both cases, the immunohistochemical staining clearly revealed a severe reduction in the number of afferent neurons, such as dendrites, spiral ganglion cells and cochlear axons. The number of efferent spiral bundles in the osseous spiral lamina and intraganglionic portion also decreased in parallel with the reduction in the number of cochlear afferent neurons. Our results are inconsistent with previously reported cases of presbycusis and acquired deafness induced by the measles virus, in which efferent neurons were preserved while afferent neurons degenerated. The loss of both the efferent and afferent neurons might be characteristics of congenital deafness.
对两名自幼患有双侧重度耳聋患者的颞骨进行了免疫组织化学研究,使用神经丝蛋白抗体检测耳蜗神经元成分。一名患者表现为内耳Mondini发育异常,柯蒂氏器几乎完全退化。另一名患者是首例报道的所有蜗管均出现柯蒂氏器完全缺如的病例。在这两个病例中,免疫组织化学染色均清楚显示传入神经元数量严重减少,如树突、螺旋神经节细胞和耳蜗轴突。骨螺旋板和神经节内部分的传出螺旋束数量也随着耳蜗传入神经元数量的减少而平行减少。我们的结果与先前报道的老年性耳聋和麻疹病毒所致后天性耳聋病例不一致,在这些病例中,传出神经元得以保留而传入神经元发生退化。传出和传入神经元均缺失可能是先天性耳聋的特征。