Suppr超能文献

表现为布朗综合征的眼外肌囊尾蚴病。

Extraocular muscle cysticercosis presenting as Brown syndrome.

作者信息

Pandey P K, Chaudhuri Z, Bhatia A

机构信息

Department of Ophthalmology, Guru Nanak Eye Centre, New Delhi, India.

出版信息

Am J Ophthalmol. 2001 Apr;131(4):526-7. doi: 10.1016/s0002-9394(00)00818-7.

Abstract

PURPOSE

Report of a case of acquired Brown syndrome caused by infestation of the superior oblique muscle by Cysticercus cellulosae.

METHOD

Case seen in a referral practice. A 20-year-old man presented with recurrent attacks of conjunctivitis and diplopia in upgaze. Clinical examination of ocular motility established a diagnosis of acquired Brown syndrome of the right eye. Computed tomography of the right orbit unequivocally established the diagnosis of superior oblique muscle cysticercosis. The patient was started on systemic steroids and albendazole in the prescribed doses for a month.

RESULT

Serial computed tomography scans of the orbit revealed resolution of the cystic lesion after a month. Clinically, although there was restoration of ocular motility in upgaze, mild restriction of movement of the right eye in levoelevation persisted. However, the patient was symptomatically better with amelioration of the recurrent conjunctivitis and diplopia in primary gaze.

CONCLUSION

Extraocular muscle cysticercosis should be considered in the differential diagnosis of acquired motility disorder. The presentation of extraocular muscle cysticercosis as an acquired Brown syndrome is unusual. Response to medical therapy was satisfactory.

摘要

目的

报告一例由猪囊尾蚴感染上斜肌导致的后天性布朗综合征病例。

方法

在转诊诊所见到的病例。一名20岁男性出现复发性结膜炎及上视时复视。眼部运动的临床检查确诊为右眼后天性布朗综合征。右眼眼眶计算机断层扫描明确诊断为上斜肌囊尾蚴病。患者开始按规定剂量服用全身性类固醇和阿苯达唑,持续一个月。

结果

眼眶的系列计算机断层扫描显示一个月后囊性病变消退。临床上,虽然上视时眼球运动恢复,但左眼上抬时右眼仍有轻度运动受限。然而,患者症状有所改善,原发性凝视时复发性结膜炎和复视有所减轻。

结论

在后天性运动障碍的鉴别诊断中应考虑眼外肌囊尾蚴病。眼外肌囊尾蚴病表现为后天性布朗综合征并不常见。药物治疗反应令人满意。

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