Inzitari D, Sità D, Marconi G P, Barontini F
J Neurol. 1981;224(3):221-8. doi: 10.1007/BF00313284.
The Tolosa-Hunt syndrome (THS) is characterized by remittent and sometimes recurring episodes of painful ophthalmoplegia. The etiopathogenesis is still unclear and is an object of controversy. A non-specific granulomatous process of the wall of the cavernous sinus is claimed by many authors as the possible cause, on the basis of a few pathological studies. Other authors suggest the possible role of autoimmune or specific inflammatory processes localized in the retroorbital perineural tissues. The clinical, laboratory and radiological findings of the eight cases reported in the agreement with those previously described in the literature. However, the visual evoked potentials (VEP) were delayed in three of the four cases in which they had been studied. This finding, together with the observation that some analogies exist between THS and other well known neuritic processes of the cranial nerves, may suggest that at least in some cases THS may be related to an ocular polyneuritis.
托洛萨-亨特综合征(THS)的特征是间歇性且有时反复出现的疼痛性眼肌麻痹发作。其发病机制仍不清楚,是一个存在争议的话题。许多作者基于一些病理学研究认为,海绵窦壁的非特异性肉芽肿性过程可能是病因。其他作者则提出自身免疫或局限于眶后神经周围组织的特异性炎症过程可能起作用。所报告的8例病例的临床、实验室和影像学检查结果与文献中先前描述的结果一致。然而,在接受研究的4例病例中,有3例的视觉诱发电位(VEP)延迟。这一发现,连同观察到THS与其他已知的颅神经神经炎过程之间存在一些相似之处,可能表明至少在某些情况下,THS可能与眼部多发性神经炎有关。