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[眼眶肌炎和托洛萨-亨特综合征的临床及神经放射学研究]

[Clinical and neuroradiological studies on orbital myositis and Tolosa-Hunt syndrome].

作者信息

Yoritaka A, Kogahara K, Yoshino H, Imai H, Mizuno Y

机构信息

Department of Neurology, Juntendo University School of Medicine.

出版信息

Rinsho Shinkeigaku. 1992 Jun;32(6):593-9.

PMID:1424337
Abstract

Tolosa-Hunt syndrome and orbital myositis have common features such as ocular pain, ophthalmoplegia and exophthalmos. Both syndromes are thought to be caused by a granulomatous inflammation involving the cavernous sinus area in the former and the orbital cavity in the latter. The question whether these two conditions represent different presentations of a single disease, or they belong to different entities has not been settled. To address this question, we reviewed our cases having clinical diagnosis of either Tolosa-Hunt syndrome or orbital myositis. Six cases were diagnosed as Tolosa-Hunt syndrome, and 7 orbital myositis. In the thin-slice enlarged orbital CT, hypertrophic and high-density changes of at least one of the extraocular muscles were found in all cases with orbital myositis, but in none of the patients with Tolosa-Hunt syndrome. The age of onset was younger and the duration of the disease before admission was shorter in Tolosa-Hunt syndrome. They responded to steroid therapy better than those with orbital myositis. These findings lead us to conclude that Tolosa-Hunt syndrome and orbital myositis belong to different syndromes, although clinical manifestations have many similarities. Then we studied the relationship between the hypertrophic change of the extraocular muscle and the direction of the oculomotor restriction. For this purpose four additional cases with dysthyroid ophthalmopathy were also studied. We found that the presence of hypertrophic change was frequently associated with the restriction of ocular movement to the direction not only of the hypertrophic muscle but also of the opposite muscle.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

托洛萨-亨特综合征和眼眶肌炎有共同特征,如眼痛、眼肌麻痹和眼球突出。这两种综合征被认为分别是由累及海绵窦区域的肉芽肿性炎症(前者)和眼眶腔的肉芽肿性炎症(后者)引起的。这两种情况是单一疾病的不同表现,还是属于不同的疾病实体,这个问题尚未解决。为了解决这个问题,我们回顾了临床诊断为托洛萨-亨特综合征或眼眶肌炎的病例。6例被诊断为托洛萨-亨特综合征,7例为眼眶肌炎。在眼眶薄层增强CT中,所有眼眶肌炎病例均发现至少一条眼外肌有肥厚和高密度改变,而托洛萨-亨特综合征患者均未出现这种情况。托洛萨-亨特综合征的发病年龄较轻,入院前病程较短。他们对类固醇治疗的反应比眼眶肌炎患者更好。这些发现使我们得出结论,尽管临床表现有许多相似之处,但托洛萨-亨特综合征和眼眶肌炎属于不同的综合征。然后我们研究了眼外肌肥厚改变与眼球运动受限方向之间的关系。为此,还研究了另外4例甲状腺功能异常性眼病患者。我们发现,肥厚改变的存在不仅常与肥厚肌肉方向的眼球运动受限有关,还与对侧肌肉方向的眼球运动受限有关。(摘要截短于250字)

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