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皮肌炎:实用指南与未满足的需求

Dermatomyositis: Practical Guidance and Unmet Needs.

作者信息

Cassard Lydia, Seraly Noelle, Riegert Maureen, Patel Aditi, Fernandez Anthony P

机构信息

Cleveland Clinic Lerner College of Medicine at Case Western Reserve University, Cleveland, OH, USA.

Department of Dermatology, Cleveland Clinic, Cleveland, OH, USA.

出版信息

Immunotargets Ther. 2024 Mar 6;13:151-172. doi: 10.2147/ITT.S381472. eCollection 2024.

Abstract

Dermatomyositis is a heterogeneous idiopathic inflammatory myopathy associated with various cutaneous manifestations and variable presence of myositis, interstitial lung disease, and other visceral organ involvement. An accurate diagnosis of dermatomyositis requires correlating clinical examination findings with serological and histological findings. Familiarity with pathognomonic and common cutaneous manifestations of dermatomyositis, which are highlighted here, can be especially helpful in making an accurate diagnosis. Additionally, evaluating patients for presence of myositis-specific autoantibodies can further support or refute a dermatomyositis diagnosis. When present, myositis-specific autoantibodies can also help guide workups for various dermatomyositis-associated manifestations, as each is associated with relatively distinct clinical characteristics. Evaluating patients for various systemic manifestations often relies on expert opinion recommendations; however, societal guideline statements concerning the evaluation of some manifestations have recently been described. Although malignancy-associated dermatomyositis is a well-accepted subtype, there is limited evidence to support extensive malignancy screening has a favorable benefit-risk ratio in most dermatomyositis patients. However, recent research has uncovered novel associations between dermatomyositis and malignancy, suggesting the possibility of identifying high-risk subsets of dermatomyositis patients in whom malignancy screening may have a high value. Treatment for dermatomyositis has remained largely unchanged over the past several decades. Although many dermatomyositis patients can be effectively treated with current options, either as monotherapy or with combination regimens, there is a need for more targeted and effective DM therapies, in general, and for MDA5(+) dermatomyositis-associated rapidly progressive interstitial lung disease. Fortunately, significant current and emerging research activities evaluating various novel medications for dermatomyositis provide hope for exciting future advances in patients with this intriguing immune-mediated disease.

摘要

皮肌炎是一种异质性特发性炎性肌病,伴有各种皮肤表现以及肌炎、间质性肺病和其他内脏器官受累情况的不同程度存在。皮肌炎的准确诊断需要将临床检查结果与血清学和组织学结果相关联。熟悉本文重点介绍的皮肌炎的特征性和常见皮肤表现,对准确诊断尤其有帮助。此外,评估患者是否存在肌炎特异性自身抗体可进一步支持或反驳皮肌炎的诊断。当存在肌炎特异性自身抗体时,还可帮助指导针对各种皮肌炎相关表现的检查,因为每种自身抗体都与相对独特的临床特征相关。评估患者的各种全身表现通常依赖专家意见建议;然而,最近已有关于某些表现评估的社会指南声明。虽然恶性肿瘤相关皮肌炎是一种公认的亚型,但在大多数皮肌炎患者中,支持广泛进行恶性肿瘤筛查具有良好获益风险比的证据有限。然而,最近的研究发现了皮肌炎与恶性肿瘤之间的新关联,提示有可能识别出恶性肿瘤筛查可能具有高价值的皮肌炎高危亚组患者。在过去几十年里,皮肌炎的治疗基本没有变化。尽管许多皮肌炎患者可以通过目前的治疗方案,无论是单药治疗还是联合治疗方案,得到有效治疗,但总体上仍需要更有针对性和更有效的皮肌炎治疗方法,尤其是针对MDA5(+)皮肌炎相关的快速进展性间质性肺病。幸运的是,目前正在进行的大量评估各种新型皮肌炎药物的研究活动以及新出现的研究活动为这种引人入胜的免疫介导疾病患者带来了令人兴奋的未来进展希望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd8/10924937/091b313e6264/ITT-13-151-g0001.jpg

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