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CT 和 MRI 中耳蜗发育不全的表现:一种新的分类。

Appearance of hypoplastic cochleae in CT and MRI: a new subclassification.

机构信息

Department of Diagnostic and Interventional Neuroradiology, Hannover Medical School, Hannover, Germany.

出版信息

Neuroradiology. 2011 Jan;53(1):49-61. doi: 10.1007/s00234-010-0777-3. Epub 2010 Oct 20.

Abstract

INTRODUCTION

Hypoplastic cochleae are among the inner ear malformations more frequently encountered by radiologists; little detailed information is available on these, however. We present the first large series of hypoplastic cochleae and document imaging findings to better characterize this anomaly radiologically.

METHODS

We used our electronic database to search for inner ear malformations described between 1995 and 2009 and extracted 81 ears (of 47 patients) with hypoplastic cochleae out of 289 patients with inner ear malformations. Two neuroradiologists evaluated the available CT and MRI data. Measurements of all inner ear structures were performed. Accompanying findings were listed.

RESULTS

Cochlear hypoplasia (58 ears, 32 patients) often involves not only the apical turn being reduced in size but also the basal turn being smaller in length. Additionally, 11 ears (eight patients) of hypoplastic cochleae with only a basal turn and five ears (four patients) of cochleae with only a small bud were identified. Non-classifiable hypoplastic cochleae (seven ears, five patients) were those with either a rudimentary or an absent basal turn or a "dwarf appearance" with no further partition.

CONCLUSIONS

The term "hypoplastic cochlea" is very general; a further division into severe and less severe forms based on the length and existence of cochlea turns is possible and can help enhance the comparison of CI outcome data. Measurements can help the less experienced radiologist to detect them more easily.

摘要

引言

发育不全耳蜗是放射科医生经常遇到的内耳畸形之一;然而,关于这些畸形的详细信息却很少。我们首次报告了一系列发育不全耳蜗,并记录了影像学表现,以便更好地对这种异常进行放射学特征描述。

方法

我们使用电子数据库检索了 1995 年至 2009 年间描述的内耳畸形,并从 289 例内耳畸形患者中提取了 81 例(47 例患者)发育不全耳蜗。两位神经放射科医生评估了现有的 CT 和 MRI 数据。对所有内耳结构进行了测量。列出了伴随的发现。

结果

耳蜗发育不全(58 例,32 例患者)不仅涉及到耳蜗顶圈的缩小,而且还涉及到基底圈的长度减小。此外,还发现了 11 例(8 例患者)仅有基底圈的发育不全耳蜗和 5 例(4 例患者)仅有小芽的发育不全耳蜗。无法分类的发育不全耳蜗(7 例,5 例患者)是指基底圈发育不全或缺失,或呈“矮小外观”,无进一步分隔。

结论

“发育不全耳蜗”一词非常笼统;根据耳蜗圈的长度和存在情况,进一步划分为严重和不严重的形式是可能的,并且可以帮助增强对人工耳蜗结果数据的比较。测量可以帮助经验较少的放射科医生更容易地检测到它们。

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