Protocolo diagnóstico de las miositis

I. Calatayud Marín , N. Abdilla Bonías , M. Calabuig Ballester , C. Arévalo-Cañas
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引用次数: 0

Abstract

Idiopathic inflammatory myopathies (IIM) are systemic autoimmune diseases characterized by progressive muscle weakness and variable extramuscular involvement. This diagnostic protocol offers a structured approach that includes a detailed clinical assessment, identification of specific autoantibodies, imaging studies, and muscle biopsy. The integration of these tools improves diagnostic accuracy, facilitates disease classification, and optimizes clinical management.
肌炎诊断方案
特发性炎症性肌病(IIM)是一种以进行性肌肉无力和可变肌外受累为特征的全身自身免疫性疾病。该诊断方案提供了一种结构化的方法,包括详细的临床评估、特异性自身抗体的鉴定、影像学研究和肌肉活检。这些工具的集成提高了诊断准确性,促进了疾病分类,并优化了临床管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
0.30
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