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通过关注主要临床线索对小脑性共济失调、神经病、前庭无反射综合征(CANVAS)进行早期诊断:超越共济失调和前庭功能障碍

Early Diagnosis in Cerebellar Ataxia, Neuropathy, Vestibular Areflexia Syndrome (CANVAS) by Focusing on Major Clinical Clues: Beyond Ataxia and Vestibular Impairment.

作者信息

Magy Laurent, Chazelas Pauline, Richard Laurence, Deschamps Nathalie, Frachet Simon, Vallat Jean-Michel, Magdelaine Corinne, Favreau Frédéric, Bessaguet Flavien, Lia Anne-Sophie, Duchesne Mathilde

机构信息

UR20218-NEURIT, Limoges University, 87000 Limoges, France.

Service de Neurologie-CHU Limoges, 87000 Limoges, France.

出版信息

Biomedicines. 2022 Aug 22;10(8):2046. doi: 10.3390/biomedicines10082046.

Abstract

CANVAS, a rare disorder responsible for late-onset ataxia of autosomal recessive inheritance, can be misdiagnosed. We investigated a series of eight patients with sensory neuropathy and/or an unexplained cough, who appeared to suffer from CANVAS, and we emphasized the clinical clues for early diagnosis. Investigations included clinical and routine laboratory analyses, skin biopsy, nerve biopsy and molecular genetics. The eight patients had clinical and/or laboratory evidence of sensory neuronopathy. All but one had neuropathic pain that had started in an asymmetric fashion in two patients. A chronic cough was a prominent feature in our eight patients and had started years before neuropathic symptoms in all but one. The course of the disease was slow, and ataxia remained mild in all. Five patients were initially thought to have immune-mediated sensory neuronopathy and received immunotherapy. Skin biopsies showed a near complete and non-length-dependent loss of intraepidermal nerve fibers. Moreover, nerve biopsy findings suggested a prominent involvement of small myelinated and unmyelinated fibers. The burden of CANVAS extends far beyond cerebellar ataxia and vestibular manifestations. Indeed, our study shows that a chronic cough and neuropathic pain may represent a major source of impairment in these patients and should not be overlooked to allow an early diagnosis and prevent unnecessary immunotherapy.

摘要

伴小脑萎缩和周围神经病的常染色体隐性遗传性感觉神经病(CANVAS)是一种罕见疾病,易被误诊。我们调查了一系列8例疑似患有CANVAS的感觉神经病和/或不明原因咳嗽患者,并强调了早期诊断的临床线索。调查包括临床和常规实验室分析、皮肤活检、神经活检和分子遗传学检查。这8例患者有感觉神经元病的临床和/或实验室证据。除1例患者外,其余患者均有神经性疼痛,其中2例患者疼痛呈不对称性发作。慢性咳嗽是我们这8例患者的一个突出特征,除1例患者外,其余患者的慢性咳嗽均在神经性症状出现数年前就已开始。疾病进展缓慢,所有患者共济失调症状均较轻。5例患者最初被认为患有免疫介导的感觉神经元病并接受了免疫免疫治疗。皮肤活检显示表皮内神经纤维几乎完全缺失且与长度无关。此外,神经活检结果提示有髓鞘小纤维和无髓鞘纤维明显受累。CANVAS的影响远不止小脑共济失调和前庭表现。事实上,我们的研究表明,慢性咳嗽和神经性疼痛可能是这些患者功能障碍的主要来源,不应被忽视,以便早期诊断并避免不必要的免疫治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4626/9405877/557ed9b2859c/biomedicines-10-02046-g001.jpg

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