Dornan T L, Espir M L, Gale E A, Tattersall R B, Worthington B S
J Neurol Neurosurg Psychiatry. 1979 Mar;42(3):270-5. doi: 10.1136/jnnp.42.3.270.
Seven patients with remittent painful ophthalmoplegia for which no specific local cause was found were seen during a period of five years. One had coincidental rheumatoid arthritis, and another had actinomycosis of the ipsilateral middle ear and contralateral parotid gland. The other five had no evidence of generalised autoimmune disease nor any other systemic disorder, two having separate episodes affecting each side. A history of relapsing and remitting painful ophthalmoplegia is suggestive of the Tolosa-Hunt syndrome, but it is rarely possible to confirm that the lesion in the cavernous sinus is the result of non-specific granulomatous infiltration so that the diagnosis remains one of exclusion. Carotid arteriography may show narrowing of the intracavernous part of the internal carotid artery. Orbital venography may also be helpful, particularly when the carotid arteriogram is normal. We believe that the Tolosa-Hunt syndrome is more common in England than is generally realised, but that its clinical features do not necessarily indicate a single pathological entity. Its recognition is important since the response to steroids, although not specific, is rapid in most patients, and the prognosis for complete recovery is relatively good.
在五年期间,我们诊治了7例缓解期疼痛性眼肌麻痹患者,未发现明确的局部病因。其中1例合并类风湿性关节炎,另1例同侧中耳及对侧腮腺放线菌病。其余5例无全身性自身免疫性疾病证据或其他任何全身性疾病,其中2例双侧均有单独发作。复发性缓解期疼痛性眼肌麻痹病史提示为托洛萨-亨特综合征,但很少能证实海绵窦病变是由非特异性肉芽肿浸润所致,因此诊断仍为排除性诊断。颈动脉造影可能显示颈内动脉海绵窦段狭窄。眼眶静脉造影也可能有帮助,尤其是当颈动脉造影正常时。我们认为托洛萨-亨特综合征在英国比普遍认为的更为常见,但其临床特征不一定表明是单一的病理实体。认识到这一点很重要,因为尽管对类固醇的反应不具有特异性,但大多数患者反应迅速,完全恢复的预后相对较好。