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与卡恩斯-塞尔综合征相关的内耳组织病理学特征。

Histopathologic features of the inner ear associated with Kearns-Sayre syndrome.

作者信息

Lindsay J R, Hinojosa R

机构信息

Department of Surgery, Pritzker School of Medicine, University of Chicago, IL 60637.

出版信息

Arch Otolaryngol. 1976 Dec;102(12):747-52. doi: 10.1001/archotol.1976.00780170065011.

Abstract

We describe the histopathologic features of the inner ear in a 19-year-old girl with bilateral total deafness associated with Kearns-Sayre syndrome. The inner ear shows advanced degree of cochleo-saccular degeneration, with almost complete absence of the organ of Corti in all turns. The spiral ganglion shows a reduction of about 60% to 70% of cells, with almost complete degeneration of nerve fibers in the bony spiral lamina. PAS-positive material was found accumulated in globules between the collapsed Reissner membrane and remains of marginal cells of the stria and in the degenerated sensory cell area of the saccular macula.

摘要

我们描述了一名19岁患有与卡恩斯-塞尔综合征相关的双侧全聋女孩内耳的组织病理学特征。内耳呈现出耳蜗-球囊的高级别退化程度,各圈几乎完全没有柯蒂氏器。螺旋神经节细胞减少约60%至70%,骨螺旋板中的神经纤维几乎完全退化。在塌陷的瑞氏膜与血管纹边缘细胞残余之间的小球以及球囊斑的退化感觉细胞区域发现有PAS阳性物质积聚。

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