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颅内脑膜瘤切除术后阵发性偏侧头痛缓解

Resolution of paroxysmal hemicrania after resection of intracranial meningioma.

作者信息

Dafer Rima M, Hocker Sara, Kumar Ragasri, McGee Jan, Jay Walter M

机构信息

Loyola University, Chicago, IL, USA.

出版信息

Semin Ophthalmol. 2010 Jan-Mar;25(1-2):34-5. doi: 10.3109/08820531003635505.

Abstract

Paroxysmal hemicrania is a trigeminal autonomic cephalalgia first described in 1976, characterized by episodic attacks of excruciating unilateral periorbital and temporal stabbing, pulsatile, craw-like, or boring headaches lasting 2 - 30 minutes, accompanied by autonomic features, and alleviated by indomethacin. Paroxysmal hemicrania is divided into an episodic or chronic form, depending on the duration and frequency of the attacks. We describe a case of paroxysmal hemicrania in a patient with a contralateral anterior clinoid meningioma, which resolved after tumor resection. Most cases of autonomic cephalgias are primary headaches and not caused by underlying intracranial structural lesions. Based on our patient and a literature review of secondary causes of trigeminal autonomic cephalalgias, we recommend that all patients with trigeminal autonomic cephalalgias including paroxysmal hemicrania undergo neuroimaging studies. The preferred neuro-radiologic procedure should be a cranial MRI to exclude underlying structural intracranial lesions, particularly in the sellar and parasellar regions.

摘要

发作性偏侧头痛是一种三叉神经自主性头痛,于1976年首次被描述,其特征为反复发作的单侧眶周和颞部剧痛,呈刺痛、搏动性、爬行样或钻痛,持续2至30分钟,伴有自主神经症状,且可通过吲哚美辛缓解。发作性偏侧头痛根据发作的持续时间和频率分为发作性或慢性形式。我们报告一例患有对侧前床突脑膜瘤的发作性偏侧头痛患者,肿瘤切除后症状缓解。大多数自主性头痛病例为原发性头痛,并非由潜在的颅内结构病变引起。基于我们的患者以及对三叉神经自主性头痛继发原因的文献综述,我们建议所有患有三叉神经自主性头痛(包括发作性偏侧头痛)的患者都应接受神经影像学检查。首选的神经放射学检查方法应为头颅MRI,以排除潜在的颅内结构病变,尤其是鞍区和鞍旁区域的病变。

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