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先天性耳道闭锁合并染色体畸变的颞骨组织病理学

Temporal bone histopathology of atresia auris congenita with chromosome aberration.

作者信息

Saito R, Fujimoto A, Fujita A, Takata N, Tomotsu T

出版信息

Acta Otolaryngol Suppl. 1983;393:96-104. doi: 10.3109/00016488309129584.

Abstract

Temporal bone findings in two infants demonstrating congenital aural atresia with microtia were presented focusing mainly on the external and middle ears. These two cases were proved to have chromosome aberration that is, 13-15 trisomy and extra chromosome in group G individually. Temporal bones showed the multiple anomalies through the external, middle and internal ears. The external canals were filled with connective tissue in one case and with bony plate in the other to form aural atresia. There were no development of the tubotympanic recess in a case of 13-15 trisomy. The oval window area in both cases was poorly developed resulting in a connective tissue fissure in the lateral wall of the vestibule except for one ear, while the round windows were normally formed in all ears. The facial nerves showed an abnormal running course without forming the geniculate ganglion and the horizontal segment. These findings indicate that the structures derived from the second branchial arch might be more deeply involved than the first one in the congenital aural atresia.

摘要

展示了两名患有先天性耳道闭锁伴小耳畸形婴儿的颞骨检查结果,主要聚焦于外耳和中耳。这两例被证实存在染色体畸变,即分别为13 - 15三体和G组额外染色体。颞骨在外耳、中耳和内耳呈现出多种异常。其中一例外耳道被结缔组织填充,另一例被骨板填充,形成耳道闭锁。在一例13 - 15三体病例中,咽鼓管鼓室隐窝未发育。两例的卵圆窗区域发育不良,除一只耳朵外,前庭侧壁形成结缔组织裂隙,而所有耳朵的圆窗均正常形成。面神经走行异常,未形成膝状神经节和水平段。这些发现表明,在先天性耳道闭锁中,源自第二鳃弓的结构可能比源自第一鳃弓的结构受累更深。

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