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继发于眼眶结构异常的非典型限制性斜视:鉴别诊断

Atypical restrictive strabismus secondary to an anomalous orbital structure: differential diagnosis.

作者信息

Merino Pilar, de Liaño Pilar Gómez, Ruiz Yolanda, Franco Gema

机构信息

Ocular Motility Section, Department of Ophthalmology, Hospital Gregorio Marañón, Madrid, Spain.

出版信息

Strabismus. 2012 Dec;20(4):162-5. doi: 10.3109/09273972.2012.702326.

DOI:10.3109/09273972.2012.702326
PMID:23211141
Abstract

Anomalous orbital structures are very rare causes of restrictive strabismus. Of the 3 types described in the literature, one involves accessory muscle fibers that are innervated by the III and/or VI cranial nerves originating in the posterior orbit and inserting on the globe, optic nerve, or extraocular muscles. Although these structures do not cause specific symptoms that enable us to make a diagnosis, we must take them into account in patients with atypical restrictive strabismus. Computed tomography and, particularly, orbital magnetic resonance imaging are essential for correct diagnosis and treatment, as the only other way to diagnose this condition is through casual findings during surgery to correct strabismus. Our patient was a child who were initially diagnosed as Duane syndrome. Magnetic resonance imaging revealed an anomalous unilateral orbital structure that limited all ocular movements except adduction, and possibly contributed to globe retraction. Surgery for strabismus did not resolve the problem: the posterior location of the orbital structure rendered surgery impossible.

摘要

异常眼眶结构是限制性斜视非常罕见的病因。在文献中描述的3种类型中,有一种涉及副肌纤维,这些纤维由起源于眼眶后部并插入眼球、视神经或眼外肌的Ⅲ和/或Ⅵ颅神经支配。尽管这些结构不会引起能让我们做出诊断的特定症状,但对于非典型限制性斜视患者,我们必须考虑到它们。计算机断层扫描,尤其是眼眶磁共振成像对于正确诊断和治疗至关重要,因为诊断这种疾病的唯一其他方法是在斜视矫正手术中偶然发现。我们的患者是一名儿童,最初被诊断为杜安综合征。磁共振成像显示一个异常的单侧眼眶结构,限制了除内收以外的所有眼球运动,并可能导致眼球后缩。斜视手术未能解决问题:眼眶结构位于后部使得手术无法进行。

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