Suppr超能文献

托洛萨-亨特综合征:一种罕见的单侧头痛和疼痛性眼肌麻痹病因的非典型表现。

Tolosa-Hunt Syndrome: A Non-Classical Presentation of a Rare Cause of Unilateral Headache and Painful Ophthalmoplegia.

作者信息

Douedi Steven, Awad Mark, Shenouda Daniel, Mack Prinze, Carson Michael P

机构信息

Department of Medicine, Jersey Shore University Medical Center, Hackensack Meridian Health, Neptune, NJ 07753, USA.

St. George University School of Medicine, St George, Grenada.

出版信息

J Clin Med Res. 2020 Apr;12(4):266-268. doi: 10.14740/jocmr4123. Epub 2020 Mar 30.

Abstract

Tolosa-Hunt syndrome is a rare condition involving the orbital and retro-orbital space. The typical symptoms are orbital pain, swelling, headache, palsies of the cranial nerves, and sensory loss in the distribution of the trigeminal nerve. Tolosa-Hunt syndrome relapses and remits with episodes separated by months to years. It is a diagnosis of exclusion after ruling out other causes of painful ophthalmoplegia and is treated with high-dose steroids. We present a case of a 43-year-old woman with a history of recurrent headaches and vision disturbances for the past 4 years presenting with worsening left-eye pain that radiated to the back of her head, swelling around the left eye, double vision, and a unilateral left-sided headache. Visual acuity was decreased in the left eye compared to the right and the patient reported left-eye pain when at extreme medial and lateral gaze. Erythrocyte sedimentation rate (ESR) was found to be elevated with all other laboratory testing within normal limits. Computed tomography (CT) scan of the orbits was unremarkable. Ophthalmology excluded other differential diagnoses and she was treated with intravenous methylprednisolone with significant improvement of symptoms. The triad of one or more episodes of unilateral orbital pain, paresis of one or more of the cranial nerves, and granulomas by magnetic resonance imaging (MRI) or biopsy is 95-100% sensitive at diagnosing the syndrome; however, our patient did not present with the "classic" triad. Initial treatment of Tolosa-Hunt is with high-dose steroids which as in our case lead to rapid and significant improvement of symptoms.

摘要

托洛萨-亨特综合征是一种累及眼眶及眶后间隙的罕见病症。典型症状包括眼眶疼痛、肿胀、头痛、颅神经麻痹以及三叉神经分布区域的感觉丧失。托洛萨-亨特综合征呈复发缓解型,发作间期为数月至数年。它是在排除其他导致疼痛性眼肌麻痹的病因后做出的诊断,治疗方法为使用大剂量类固醇。我们报告一例43岁女性病例,该患者在过去4年中有复发性头痛和视力障碍病史,此次表现为左眼疼痛加剧并放射至后脑勺、左眼周围肿胀、复视以及单侧左侧头痛。与右眼相比,左眼视力下降,患者报告在向最内侧和最外侧注视时左眼疼痛。红细胞沉降率(ESR)升高,其他所有实验室检查均在正常范围内。眼眶计算机断层扫描(CT)未发现异常。眼科排除了其他鉴别诊断,患者接受静脉注射甲泼尼龙治疗,症状有显著改善。单侧眼眶疼痛发作一次或多次、一条或多条颅神经麻痹以及磁共振成像(MRI)或活检显示肉芽肿这三者构成的三联征在诊断该综合征时敏感性为95%-100%;然而,我们的患者并未出现“经典”三联征。托洛萨-亨特综合征的初始治疗是使用大剂量类固醇,就像我们的病例一样,这导致症状迅速且显著改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4330/7188369/6797f788a810/jocmr-12-266-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验