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筛窦静息性窦综合征致眼眶内移:病例报告

Ethmoid silent sinus syndrome causing inward displacement of the orbit: case report.

作者信息

McArdle B, Perry C

机构信息

Division of Surgery, Gold Coast Hospital, Southport, Australia.

出版信息

J Laryngol Otol. 2010 Feb;124(2):206-8. doi: 10.1017/S0022215109990521. Epub 2009 Jul 17.

Abstract

OBJECTIVE

We describe a previously unreported case of ethmoid silent sinus syndrome.

METHOD

Case report and review of the world literature regarding silent sinus syndrome.

RESULTS

A 33-year-old woman developed medial displacement of the left orbital contents in the absence of trauma, surgery or other significant pathology. Imaging showed opacification of the left ethmoid sinus and implosion of the medial orbital wall. Previously reported cases of silent sinus syndrome have all involved the maxillary sinus, with subsequent implosion of the orbital floor. Computed tomography scans of our patient showed wide, flat ethmoidal bulla and surrounding cells, with few horizontal bony septae reinforcing the area of collapse.

CONCLUSION

This case represents the first report of ethmoid silent sinus syndrome. We argue that, in anatomically susceptible individuals, the silent sinus syndrome can present due to chronic ethmoidal sinusitis.

摘要

目的

我们描述一例此前未报道过的筛窦隐匿性鼻窦综合征病例。

方法

病例报告及对有关隐匿性鼻窦综合征的世界文献进行综述。

结果

一名33岁女性在无外伤、手术或其他重大病变的情况下出现左眶内容物向内侧移位。影像学检查显示左侧筛窦混浊及眶内侧壁内陷。此前报道的隐匿性鼻窦综合征病例均累及上颌窦,随后眶底内陷。我们患者的计算机断层扫描显示筛泡宽大扁平,周围气房较少,水平骨隔较少,难以加固塌陷区域。

结论

该病例是筛窦隐匿性鼻窦综合征的首例报告。我们认为,在解剖结构易患个体中,隐匿性鼻窦综合征可能由慢性筛窦炎引起。

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