Hannerz J, Ericson K, Bergstrand G
Cephalalgia. 1986 Mar;6(1):59-63. doi: 10.1046/j.1468-2982.1986.0601059.x.
The Tolosa-Hunt syndrome is characterized by recurrent periods of painful ophthalmoplegia, dramatically ameliorated by steroid treatment. In half of the cases orbital phlebography shows characteristic changes. Ninety-six patients with orbital pain characteristic of the Tolosa-Hunt syndrome were submitted to orbital phlebography regardless of the existence of other symptoms. A pathologic phlebogram with changes typical of the Tolosa-Hunt syndrome was found in 50 patients. In 17 of these 50 patients the symptoms consisted of orbital pain only and no ophthalmoplegia. Twenty patients had pain and ipsilateral decrease of vision but no ophthalmoplegia, and 13 had painful ophthalmoplegia. Of 41 patients treated with steroid medication 39 responded dramatically with regard to the pain. Earlier findings indicate that the phlebographic changes are due to venous vasculitis, which thus may cause irreversible visual impairment but also chronic headache without ophthalmoplegia. It is concluded that the Tolosa-Hunt syndrome may be only one manifestation of a not uncommon disease.
托洛萨-亨特综合征的特征是反复出现疼痛性眼肌麻痹,类固醇治疗可使其显著改善。半数病例的眼眶静脉造影显示有特征性改变。96例有托洛萨-亨特综合征典型眼眶疼痛的患者接受了眼眶静脉造影,无论是否存在其他症状。50例患者发现有典型托洛萨-亨特综合征改变的病理性静脉造影。在这50例患者中,17例症状仅为眼眶疼痛,无眼肌麻痹。20例有疼痛及同侧视力下降但无眼肌麻痹,13例有疼痛性眼肌麻痹。在41例接受类固醇药物治疗的患者中,39例疼痛症状得到显著缓解。早期研究结果表明,静脉造影改变是由静脉血管炎引起的,因此可能导致不可逆的视力损害,也可能导致无眼肌麻痹的慢性头痛。结论是,托洛萨-亨特综合征可能只是一种并不罕见疾病的一种表现形式。