头痛伴脑神经麻痹——三例诊断和治疗的挑战

Jakab Erika, Rokaly Gabriella, Balla Antal, Albert Orsolya, Mihály István, Szász József Attila, Szatmári Szabolcs
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摘要

头痛是神经内科最常见的主诉之一。作为一种症状,头痛不仅是患者的问题,也是医生的问题,因为除了原发性头痛之外,继发性头痛可以有各种病因。在原发性头痛中,偏头痛和丛集性头痛可表现为颅神经症状。继发性头痛的鉴别诊断是困难的。我们必须包括血管、肿瘤、感染、炎症、毒性、自身免疫等原因,这些原因的诊断需要复杂的实验室和/或影像学检查,而没有异常发现往往提示自身免疫或不明原因。在我们的回顾中,我们的目的是提出三个病例,其中头痛与颅神经受累,主要是眼麻痹。3例患者病程均较长,特点为无症状期交替出现阵发性头痛和多种脑神经麻痹。最常见的是动眼神经和外展脑神经麻痹,但三叉神经和面神经也会受累。根据症状,这三个病例都怀疑海绵窦病变,然而,这无法通过先进的神经影像学技术证实。除了对症治疗外,类固醇治疗改善了症状,但并非所有病例的神经症状都消失了。此外,这些症状在短时间内或不同的脑神经受累后再次出现。缺乏积极的诊断,疾病的波动过程和类固醇治疗的副作用需要长期随访,这只有通过适当的医患关系才能实现。由于这些病例的指导方针难以详细说明,因此需要不断重新评估诊断和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Headache with cranial nerve palsy – a diagnostic and therapeutic challenge in three cases
Abstract Headaches are among the most common complaints in the Neurology Clinic. As a symptom, headache is often a problem not only for the patient, but also for the doctor, as in addition to primary headaches, secondary headaches can have various etiologies. Among the primary headaches, migraine and cluster headaches may present cranial nerve symptoms. The differential diagnosis of secondary headaches can be difficult. We have to include vascular, neoplastic, infectious, inflammatory, toxic, autoimmune causes, where diagnosis requires complex laboratory and/or imaging studies, while the absence of abnormal findings often suggests autoimmune or unknown origin. In our review, we aim to present three cases where the headache was associated with cranial nerve involvement, mainly ophthalmoparesis. The course of the disease was long in all three cases, characterized by symptom-free periods alternating with paroxysmal headaches and diverse cranial nerve palsies. Most frequently, the oculomotor and abducent cranial nerve palsies were observed, but the involvement of trigeminal and facial nerves occurred as well. Based on the symptoms, there was a suspicion of a lesion of the cavernous sinus in all three cases, however, this couldn’t be confirmed by advanced neuroimaging techniques. In addition to symptomatic treatment, steroid therapy improved the complaints, but neurological signs did not disappear in all cases. Furthermore, the signs reappeared after a short time or a different cranial nerve was involved. The lack of a positive diagnosis, the fluctuating course of the disease, and the side effects of steroid therapy demand a long-term follow-up, which is possible only through an appropriate doctor-patient relationship. As guidelines are difficult to elaborate on for such cases, continuous re-evaluation of diagnosis and treatment are required.
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