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模仿眼肌麻痹性偏头痛的动眼神经鞘瘤

Oculomotor nerve schwannoma mimicking ophthalmoplegic migraine.

作者信息

Murakami T, Funatsuka M, Komine M, Hirayama Y, Suzuki H, Shishikura K, Aihara Y, Shibata K, Hori T, Kobayashi M, Osawa M

机构信息

Department of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan.

出版信息

Neuropediatrics. 2005 Dec;36(6):395-8. doi: 10.1055/s-2005-873056.

Abstract

Ophthalmoplegic migraine (OM) is a rare variant of migraine characterized by recurrent attacks of severe headache followed by oculomotor nerve palsy. The recent revision of the International Headache Classification has reclassified OM from a subtype of migraine, defined as a functional headache, to the neuralgia category. We describe a case of an 11-year-old girl with pathologically confirmed oculomotor nerve schwannoma who had been suffering from symptoms mimicking OM. For five years, she has been under treatment for OM, an initial diagnosis which was corroborated by brain magnetic resonance imaging (MRI). Usually, most OM attacks occur during one period in a lifetime and remit completely. In contrast, however, her attacks became more frequent and were not controlled by medication. After surgery, the frequency of OM attacks was reduced. From this experience, we hypothesize that optic nerve tumor is one condition that can mimic OM, without apparent signs suggestive of intracranial mass. To our knowledge, this is the first report to describe a pathologically confirmed case of oculomotor nerve schwannoma mimicking OM.

摘要

眼肌麻痹性偏头痛(OM)是偏头痛的一种罕见变异型,其特征为严重头痛反复发作,随后出现动眼神经麻痹。国际头痛分类的最新修订已将OM从偏头痛的一个亚型(定义为功能性头痛)重新分类到神经痛类别。我们描述了一例11岁女孩,经病理证实患有动眼神经鞘瘤,她一直有类似OM的症状。五年来,她一直在接受OM的治疗,最初的诊断得到了脑磁共振成像(MRI)的证实。通常,大多数OM发作在一生中的某个时期出现一次,并完全缓解。然而,与之相反的是,她的发作变得更加频繁,且药物无法控制。手术后,OM发作的频率降低了。从这一经验中,我们推测视神经肿瘤是一种可模拟OM的疾病,且无明显提示颅内肿块的体征。据我们所知,这是第一份描述经病理证实的动眼神经鞘瘤模拟OM病例的报告。

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