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双侧后半规管发育不全与非典型阵发性位置性眩晕:一例报告

Bilateral posterior semicircular canal aplasia and atypical paroxysmal positional vertigo: a case report.

作者信息

Walther L E, Nath V, Krombach G A, Di Martino E

机构信息

Centre of Otorhinolaryngology, Sulzbach, Germany.

出版信息

Acta Otorhinolaryngol Ital. 2008 Apr;28(2):79-82.

Abstract

Isolated congenital malformations of semicircular canals are rare abnormalities. Most inner ear abnormalities occur in syndromes and are associated with hearing loss. Unilateral or bilateral single aplasia of one semicircular canal does not usually result in vertigo, but these become clinically important if there are clinical complaints of vertigo. Computed tomography imaging and high resolution magnetic resonance imaging may reveal inner ear abnormalities. The case is presented here of a 46-year-old male with a 10-year history of recurrent positional vertigo with strong onset when changing position to the left side. Magnetic resonance imaging of the inner ear showed a bilateral posterior semicircular canal aplasia as well as an enlarged vestibule on both sides. Dix-Hallpike positional manoeuvre revealed a positional nystagmus in the left head-hanging position of short duration and latency of a few seconds. When rising, vertigo occurred, but no nystagmus was visible. The fast phase of the nystagmus was mainly vertical down-beating with a slight torsional component to the uppermost ear. Although benign paroxysmal vertigo of the anterior canal was suspected, physical therapy was not effective using a modified liberatory manoeuvre. Brandt-Daroff therapy was effective permanently.

摘要

孤立性半规管先天性畸形是罕见的异常情况。大多数内耳异常发生于综合征中,并与听力损失相关。单侧或双侧单个半规管发育不全通常不会导致眩晕,但如果有眩晕的临床主诉,这些情况就具有临床重要性。计算机断层扫描成像和高分辨率磁共振成像可能会揭示内耳异常。本文介绍了一例46岁男性患者,有10年复发性位置性眩晕病史,向左翻身时发作强烈。内耳磁共振成像显示双侧后半规管发育不全以及双侧前庭扩大。Dix-Hallpike位置试验显示在左侧悬头位出现持续时间短、潜伏期为几秒的位置性眼震。起身时出现眩晕,但未观察到眼震。眼震的快相主要为垂直向下跳动,向最高耳侧有轻微扭转成分。尽管怀疑是前半规管良性阵发性眩晕,但采用改良的Epley法进行物理治疗无效。Brandt-Daroff训练法有永久性疗效。

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A new classification for cochleovestibular malformations.一种新的耳蜗前庭畸形分类法。
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