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耳廓正常或I级小耳畸形且外耳道单侧轻度狭窄患儿的高分辨率CT表现

High-resolution CT findings in children with a normal pinna or grade I microtia and unilateral mild stenosis of the external auditory canal.

作者信息

Jacob R, Gupta S, Isaacson B, Kutz J W, Roland P, Xi Y, Booth T N

机构信息

From the Departments of Radiology (R.J., Y.X., T.N.B.).

Otolaryngology (S.G., B.I., J.W.K., P.R.), Children's Medical Center of Dallas, University of Texas, Southwestern Medical Center, Dallas, Texas.

出版信息

AJNR Am J Neuroradiol. 2015 Jan;36(1):176-80. doi: 10.3174/ajnr.A4067. Epub 2014 Aug 14.

Abstract

A subset of patients presents with unilateral conductive hearing loss, a normal pinna or grade I microtia, and mild external auditory canal stenosis. The physical findings of microtia and a small external canal are commonly absent or subtle in this group of patients, who are being commonly referred for imaging to evaluate isolated conductive hearing loss. We present a case series of patients with unilateral conductive hearing loss and characteristic ossicular abnormalities, commonly anterior fixation of the malleus. All patients had a significantly increased distance from the cochlear promontory to the handle of the malleus and an abnormal incudostapedial angle, indicative of an abnormal ossicular position and/or morphology. Successful surgical reconstruction of the ossicular chain was attempted and accomplished in 3 patients.

摘要

一部分患者表现为单侧传导性听力损失、耳廓正常或 I 级小耳畸形以及轻度外耳道狭窄。在这组患者中,小耳畸形和外耳道狭小的体格检查结果通常不明显或很细微,他们通常因孤立性传导性听力损失而被转诊进行影像学检查。我们报告了一组单侧传导性听力损失且伴有特征性听骨链异常(通常为锤骨前方固定)的患者病例系列。所有患者从蜗窗岬到锤骨柄的距离均显著增加,砧镫关节角异常,提示听骨链位置和/或形态异常。3 例患者尝试并成功完成了听骨链的手术重建。

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本文引用的文献

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Otolaryngol Head Neck Surg. 2012 Aug;147(2):323-8. doi: 10.1177/0194599812442866. Epub 2012 Mar 30.
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Isolated congenital ossicular anomalies.孤立性先天性听小骨异常
Acta Otolaryngol. 2009 Apr;129(4):419-22. doi: 10.1080/00016480802587846.
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Surgical management of conductive hearing loss in children.
Otolaryngol Clin North Am. 2002 Aug;35(4):853-75. doi: 10.1016/s0030-6665(02)00054-3.

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