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关于耳蜗 - 肾综合征发病机制的思考(作者译)

[Considerations on the pathogenesis of the cochleo-renal syndrome (author's transl)].

作者信息

Arnold W

出版信息

Acta Otolaryngol. 1980 Mar-Apr;89(3-4):330-41. doi: 10.3109/00016488009127145.

Abstract

The histological findings in two cases of Alport's syndrome are presented. Damage within the inner ear is mainly represented in the vascular stria region and it seems that the inner ear damage pattern tallies with the renal alterations. Glomerular basement thickening and splitting are the first and pathognomonic findings together with confluence of the epithelial feet. Later on, the increase in volume in the epithelial cells and the tremendous enlargement of the glomerular basement membranes leads to an obliteration of glomerular capillaries. In the first described case a subtotal loss of stria vascularis seems to be the reason for a degeneration of the inner and outer hair cells as well as of some spiral ganglion cells. The second case revealed only a slight edema of the stria vascularis and apical protrusions of cytoplasm, sometimes vacuolated. Whereas in the basal turn most of the inner hair cells had disappeared, in the upper turns we observed a slight degeneration of the inner hair cell but intact outer hair cell system. Although in Alport's syndrom there are--according to the literature--no constant findings, our observations allow us to assume that inner ear damage in the cochleo-renal syndrome is secondary to the kidney disease.

摘要

本文报告了两例Alport综合征的组织学研究结果。内耳损伤主要表现在血管纹区域,且内耳损伤模式似乎与肾脏病变相符。肾小球基底膜增厚和分层是最早出现的特征性表现,同时伴有上皮足突融合。随后,上皮细胞体积增大以及肾小球基底膜极度增厚导致肾小球毛细血管闭塞。在首例病例中,血管纹大部分缺失似乎是内、外毛细胞以及部分螺旋神经节细胞退变的原因。第二例仅显示血管纹轻度水肿以及细胞质顶端突起,有时呈空泡状。在蜗管底部,大部分内毛细胞消失,而在上部蜗管,我们观察到内毛细胞轻度退变,但外毛细胞系统完整。尽管根据文献报道,Alport综合征并无固定表现,但我们的观察结果使我们推测,肾-耳综合征中的内耳损伤是肾脏疾病的继发表现。

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