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[功能性血管性肢端综合征]

[Functional vascular acrosyndromes].

作者信息

Klein-Weigel Peter, Ruttloff Andreas, König Dana, Nielitz Jessica, Steindl Julia, Sander Oliver, Richter Jutta G

机构信息

Klinik für Angiologie, Klinikum Ernst von Bergmann, Charlottenstr. 72, 14467, Potsdam, Deutschland.

Poliklinik und Funktionsbereich für Rheumatologie & Hiller-Forschungszentrum für Rheumatologie, Universitätsklinikum Düsseldorf, Medizinische Fakultät, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Deutschland.

出版信息

Inn Med (Heidelb). 2022 Jun;63(6):591-600. doi: 10.1007/s00108-022-01340-w. Epub 2022 May 16.

Abstract

Vascular acrosyndromes are characterized by sparse, uniform clinical manifestations and a variety of possible pathomechanisms. The present article focuses on the functional entities. Raynaud phenomenon is based on cold- or stress-induced vasospasms of acral arteries. It is defined by the color changes of the skin, in the typical case white-blue-red (tricolore). The long fingers are most commonly affected. The etiology is unknown, and the pathophysiology is poorly understood. A distinction is made between primary and a secondary Raynaud phenomenon. The most important underlying diseases include collagenosis, primarily systemic sclerosis, and malignancies; furthermore, medications and drugs may promote vasospasm. Treatment is aimed at preventing or breaking the vasospasm, but has been only partially effective in doing so. Acrocyanosis is a vasospastic dystonic acral disorder that results in permanent reddish-livid discoloration, especially of the hands and feet. Secondary forms occur in collagenosis, malignancies, and myelodysplastic syndromes. The etiology and pathophysiology are virtually unknown. Targeted pharmacological intervention is not possible. Unlike all other vascular acrosyndromes, erythromelalgia is characterized by hyperemia. The primary form is a genetic sodium channelopathy, while secondary forms include malignancies, connective tissue diseases, and myelodysplastic syndromes. The symptoms are often distressing and disabling. Therapy requires a multimodal approach that includes both nonpharmacological and pharmacological strategies. Close interdisciplinary collaboration is essential for the management of this disease.

摘要

血管性肢端综合征的特点是临床表现稀少且一致,有多种可能的发病机制。本文重点关注功能实体。雷诺现象基于寒冷或压力诱导的肢端动脉血管痉挛。它由皮肤颜色变化定义,典型病例为白-蓝-红(三色)。手指长的人最常受累。病因不明,病理生理学也知之甚少。原发性和继发性雷诺现象有所区分。最重要的潜在疾病包括胶原病,主要是系统性硬化症和恶性肿瘤;此外,药物可能会促进血管痉挛。治疗旨在预防或打破血管痉挛,但仅部分有效。手足发绀症是一种血管痉挛性张力障碍性肢端疾病,会导致永久性的微红-青紫变色,尤其是手和脚。继发性形式见于胶原病、恶性肿瘤和骨髓增生异常综合征。病因和病理生理学几乎未知。无法进行有针对性的药物干预。与所有其他血管性肢端综合征不同,红斑性肢痛症的特征是充血。原发性形式是一种遗传性钠通道病,而继发性形式包括恶性肿瘤、结缔组织病和骨髓增生异常综合征。症状往往令人痛苦且致残。治疗需要多模式方法,包括非药物和药物策略。密切的跨学科合作对于管理这种疾病至关重要。

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