Tolosa-Hunt syndrome: a review of diagnostic criteria based on a case series.

Postepy psychiatrii neurologii Pub Date : 2024-03-01 Epub Date: 2024-02-12 DOI:10.5114/ppn.2023.135176
Piotr R Chądzyński, Katarzyna Stopińska, Izabela Domitrz
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Abstract

Purpose: Tolosa-Hunt syndrome (THS) is a rare cause of painful ophtalmoplegia with different clinical manifestations. It is described as a unilateral periorbital headache with concomitant dysfunction of at least one out of the IIIrd, IVth and VIth cranial nerves due to the granulomatous inflammation of periorbital structures, but no underlying cause has been established.

Case description: We present six patients referred to the Neurology Department due to a unilateral headache with ipsilateral paresis of at least one cranial nerve responsible for eye movements. The THS diagnostic criteria of the International Headache Disorders Classification (ICHD-3) were applied and analysed. Few patients had atypical clinical manifestations according to these criteria.

Comment: Diagnosing THS may prove very challenging. There is a lack of specific markers for the disorder, whereas diagnostic criteria leave a wide area for misdiagnosis. The diagnostic approach should be focused on the exclusion of other pathologies because typical steroid therapy may prove fatal in otherwise benign cases.

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托洛萨-亨特综合征:基于系列病例的诊断标准回顾。
目的:托罗莎-亨特综合征(THS)是一种罕见的引起疼痛性眼睑麻痹的疾病,临床表现各不相同。它被描述为由于眶周结构肉芽肿性炎症引起的单侧眶周头痛,同时伴有第 III、IV 和 VI 颅神经中至少一条神经的功能障碍,但其根本原因尚未确定:我们介绍了六名因单侧头痛且同侧至少有一条负责眼球运动的颅神经瘫痪而转诊至神经内科的患者。我们采用了国际头痛疾病分类(ICHD-3)的 THS 诊断标准并对其进行了分析。根据这些标准,极少数患者有不典型的临床表现:评论:THS 的诊断可能极具挑战性。评论:THS 的诊断可能非常具有挑战性,因为这种疾病缺乏特异性的标记物,而诊断标准又为误诊留下了广阔的空间。诊断方法应侧重于排除其他病症,因为典型的类固醇治疗可能会对原本良性的病例造成致命伤害。
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