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瓦登伯革氏综合征的颞骨组织病理学发现:一例报告

Temporal bone histopathologic findings of Waardenburg's syndrome: a case report.

作者信息

Nakashima S, Sando I, Takahashi H, Hashida Y

机构信息

Elizabeth McCullough Knowles Otopathology Laboratory, University of Pittsburgh School of Medicine, PA.

出版信息

Laryngoscope. 1992 May;102(5):563-7. doi: 10.1288/00005537-199205000-00016.

Abstract

A histopathological study of the temporal bones of a 3-year-old black girl who had bilateral deafness associated with Waardenburg's syndrome type II showed a similar pattern of pathology in both ears. The most striking findings were an absence of pigmentation in the inner ear and cochleosaccular abnormality. This is, to our knowledge, only the third report on human temporal bone histopathology in Waardenburg's syndrome and the first report of such a case with absence of pigment (melanin) in the inner ear. A possible association of hearing loss with absence of inner ear pigment in this case is discussed.

摘要

对一名患有与II型瓦登伯革氏综合征相关的双侧耳聋的3岁黑人女孩的颞骨进行的组织病理学研究显示,双耳的病理模式相似。最显著的发现是内耳无色素沉着以及耳蜗球囊异常。据我们所知,这是关于瓦登伯革氏综合征中人类颞骨组织病理学的第三篇报告,也是首例内耳无色素(黑色素)的此类病例报告。本文讨论了该病例中听力损失与内耳无色素沉着之间可能的关联。

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