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首页> 外文期刊>The neurologist. >Peripheral nervous system manifestations of Sjogren syndrome: clinical patterns, diagnostic paradigms, etiopathogenesis, and therapeutic strategies.
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Peripheral nervous system manifestations of Sjogren syndrome: clinical patterns, diagnostic paradigms, etiopathogenesis, and therapeutic strategies.

机译:Sjogren综合征的周围神经系统表现:临床模式,诊断范式,病因和治疗策略。

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摘要

Sjogren syndrome is among the most common autoimmune diseases affecting adults in the United States, and is frequently regarded as an immune-mediated exocrinopathy exclusively causing dry eyes and dry mouth. However, as a systemic rheumatic disease, there can be various "extraglandular" complications. The eclectic permutation of peripheral nervous system (PNS) syndromes which occur in Sjogren patients are among the most common and severe extraglandular complications. This review article highlights the evaluation, differential diagnosis, immunopathogenic mechanisms, and potential treatment options of these PNS complications encountered by neurologists. The sensory neuropathies constitute the most frequent PNS complication. Sjogren patients can suffer from severe neuropathic pain, with small-fiber neuropathy causing lancinating or burning pain which can disproportionately affect the proximal torso or extremities, and the face (ie, in a "non-length-dependent distribution"). The technique of skin biopsy, assessing for the intraepidermal nerve fiber density of unmyelinated nerves, provides a useful technique for neurologists to diagnose small-fiber neuropathies, especially when there is such a non-length-dependent distribution. Other diagnostic techniques (ie, electromyographyerve-conduction studies, evoked potentials, nerve and muscle biopsy) may be useful in specific subtypes of neuropathies. A rational approach to treatment requires a careful appraisal of the clinical subtype of the neuropathy, as well as a familiarity with such discriminating immunopathogenic mechanisms. The application of the traditional armamentarium used for neuropathic pain can be especially challenging. Sjogren patients can suffer from debilitating fatigue, sicca symptoms, and autonomic findings; as such manifestations can be complications of various neuropathic agents, neurologists should understand how to minimize such iatrogenic complications. Therefore, this article will empower neurologists to more effectively collaborate with rheumatologists, in the diagnosis and treatment of Sjogren patients with PNS complications.
机译:干燥综合征是在美国影响成年人的最常见的自身免疫疾病之一,通常被认为是一种免疫介导的外分泌病,仅引起眼睛干燥和口干。但是,作为系统性风湿病,可能会出现各种“腺外”并发症。 Sjogren患者中发生的周围神经系统(PNS)综合征折衷排列是最常见和最严重的腺外并发症之一。这篇综述文章重点介绍了神经科医生对这些PNS并发症的评估,鉴别诊断,免疫病理机制和潜在的治疗选择。感觉神经病是最常见的PNS并发症。干燥的患者可能会遭受严重的神经病性疼痛,小纤维神经病会导致变瘦或灼痛,这会严重影响近端躯干或四肢以及面部(即“非长度依赖性分布”)。皮肤活检技术,评估无髓神经的表皮内神经纤维密度,为神经科医生诊断小纤维神经病提供了一种有用的技术,特别是当存在这种非长度依赖性分布时。其他诊断技术(即肌电图/神经传导研究,诱发电位,神经和肌肉活检)可能对特定的神经病亚型有用。合理的治疗方法需要仔细评估神经病变的临床亚型,并熟悉这种区分性免疫病原性机制。传统武器库用于神经性疼痛的应用可能尤其具有挑战性。 Sjogren患者可能会出现虚弱的疲劳,干燥症状和自主神经发现。由于这种表现可能是各种神经性疾病的并发症,神经科医生应了解如何最大程度地减少此类医源性并发症。因此,本文将使神经科医生能够更有效地与风湿病学家合作,以诊断和治疗Sjogren患有PNS并发症的患者。

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