Inflammatory myopathies and overlap syndromes: Update on histological and serological profile

被引：19

作者：

Colafrancesco, Serena ^{[1
]}

Priori, Roberta ^{[1
]}

Valesini, Guido ^{[1
]}

机构：

[1] Univ Roma La Sapienza, Dipartimento Med Interna & Specialita Med, UOC Reumatol, Policlin Umberto 1,Viale Policlin 155, I-00161 Rome, Italy

来源：

BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY | 2015年 / 29卷 / 06期

关键词：

Myositis; Overlap; Autoantibodies; Biopsy; Histology; PRIMARY SJOGRENS-SYNDROME; INCLUSION-BODY MYOSITIS; CANCER-ASSOCIATED DERMATOMYOSITIS; PROGRESSIVE SYSTEMIC-SCLEROSIS; MUSCLE INVOLVEMENT; SKELETAL-MUSCLE; RHEUMATOID-ARTHRITIS; LUPUS-ERYTHEMATOSUS; AUTOANTIBODIES; POLYMYOSITIS;

D O I：

10.1016/j.berh.2016.02.005

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

The term 'inflammatory myopathies' (IMs) comprise a group of muscle diseases formed by four main categories known as polymyositis (PM), dermatomyositis (DM), inclusion body myositis (IBM) and immune-mediated necrotizing myopathy (IMNM). Due to the increasing evidence of IMs over the course of different autoimmune diseases, the overlap myositis (OM) has been recently recognized as a possible stand-alone entity. IMs are characterized by a wide spectrum of autoantibodies, and the panel of myositis-associated autoantibodies (MAA) has dramatically increased over the last years giving the clinicians a further crucial support to differentiate the different types of myositis. This study aims to collect the most relevant evidence published up to date on the most commonly described OM with a particular emphasis on their histological aspects and also serological features. (C) 2016 Elsevier Ltd. All rights reserved.

引用

页码：810 / 825

页数：16

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