医学
鉴别诊断
疾病
病理
重症监护医学
颅神经
外科
血管疾病
罕见病
皮肤病科
退行性疾病
体征和症状
全身性疾病
生物信息学
作者
L.V. Reznikova,M.B. Kuchminskaya,Л В Шерстнева,A.E. Aslamazova
标识
DOI:10.17116/oftalma2025141061114
摘要
Tolosa-Hunt syndrome (THS) is a rare neuro-ophthalmological pathology caused by nonspecific granulomatous inflammation in the area of the cavernous sinus, which leads to painful ocular motility restrictions and ophthalmoplegia. The disease is characterized by lesions of the III, IV, and VI cranial nerves, with possible extension to branches of the V nerve and oculosympathetic fibers. This review analyses current data on this disease, with emphasis on its clinical presentation, diagnostic criteria and treatment methods. Taking into account the complexity of identifying THS, emphasis is made on the need for careful differential diagnosis with other clinically similar conditions, such as brain tumors, vascular aneurysms, inflammatory processes, etc. Timely detection of the syndrome and initiation of appropriate treatment, including the use of glucocorticoid hormones, can help prevent serious complications in the form of vision loss or permanent impairment of ocular motor function.
科研通智能强力驱动
Strongly Powered by AbleSci AI