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与肾发育不全和免疫缺陷疾病相关的耳部异常。一项组织病理学研究。

Ear anomalies associated with renal dysplasia and immunodeficiency disease. A histopathological study.

作者信息

Lindsay J R, Hinojosa R

出版信息

Ann Otol Rhinol Laryngol. 1978 Jan-Feb;87(1 Pt 1):10-7. doi: 10.1177/000348947808700103.

Abstract

The histopathologic study of the temporal bones of a case with low-set rudimentary auricles, without preauricular pits or cervical fistula is presented. Abnormalities of the middle and inner ear, fusion of the kidneys, hydrocephalus, short-limbed dwarfism and immunodeficiency are described. An abnormally low position of the middle cranial fossa in relation to the petrous pyramid was observed. The cochlea was of normal length. The modiolus was poorly developed with apparently normal population of ganglion cells and moderate diffuse hydrops of the cochlear duct and saccule. The stria vascularis was partially degenerated in the upper apical coil. Vestibular abnormalities included bilateral absence of common crus of the vertical canals and unusually high origin of endolymphatic aqueduct with no medial dilation present, the convoluted portion of the sac located beneath the dura.

摘要

本文报告了一例双侧耳廓低位且发育不全、无耳前凹或颈瘘患者颞骨的组织病理学研究。描述了中耳和内耳的异常、肾脏融合、脑积水、短肢侏儒症和免疫缺陷。观察到中颅窝相对于岩锥的位置异常低。耳蜗长度正常。蜗轴发育不良,神经节细胞数量明显正常,耳蜗管和球囊有中度弥漫性积水。血管纹在上部顶圈部分退化。前庭异常包括双侧垂直半规管总脚缺如,内淋巴管起始异常高且无内侧扩张,囊的盘曲部分位于硬脑膜下方。

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