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特纳综合征中的蒙迪尼畸形。一篇颞骨报告。

The Mondini defect in Turner's syndrome. A temporal bone report.

作者信息

Windle-Taylor P C, Buchanan G, Michaels L

出版信息

Clin Otolaryngol Allied Sci. 1982 Apr;7(2):75-80. doi: 10.1111/j.1365-2273.1982.tb01566.x.

Abstract

The histopathology of the right temporal bone of a 47 year old deaf woman with Turner's Syndrome (gonadal dysgenesis) is described. The appearances are of the Mondini deformity, the cochlea consisting of a single basal turn with a bulbous apical dilatation. The organ of Corti was absent. The remainder of the bony labyrinth save for the cochlear aqueduct was normal. The patient's death was due to a cerebral astrocytoma. Previous reports concerning the co-existence of gonadal dysgenesis, congenital deafness and non-gonadal neoplasia are discussed.

摘要

描述了一名患有特纳综合征(性腺发育不全)的47岁失聪女性右颞骨的组织病理学情况。其表现为蒙迪尼畸形,耳蜗由单一的基底转和球根状的顶端扩张组成。柯蒂氏器缺失。除蜗水管外,骨迷路的其余部分正常。患者死于脑星形细胞瘤。文中讨论了此前关于性腺发育不全、先天性耳聋和非性腺肿瘤并存的报告。

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