Inflammatory myopathies, autoimmune necrotizing myopathies and adult-onset genetic myopathies: Differential diagnosis

被引：10
作者：
Dimitri, D. [1 ]
Eymard, B. [2 ]
机构：
[1] CHU Henri Mondor, AP HP, Ctr Reference Malad Neuromusculaires Garches N, Serv Histol, F-94010 Creteil, France
[2] CHU Pitie Salpetriere, AP HP, Ctr reference Malad Neuromusculaires Paris Est, F-75651 Paris, France
来源：
REVUE DE MEDECINE INTERNE | 2012年 / 33卷 / 03期
关键词：
Inflammatory myopathies; Autoimmune necrotizing myopathy; Muscular dystrophies; Dysferlinopathy; Late-onset nemaline myopathy; INCLUSION-BODY MYOSITIS; BENT SPINE SYNDROME; MUSCULAR-DYSTROPHY; NEMALINE MYOPATHY; DISTAL MYOPATHY; MYOTONIC-DYSTROPHY; UP-REGULATION; POLYMYOSITIS; MUTATIONS; DISEASE;
D O I：
10.1016/j.revmed.2011.11.018
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
The inflammatory myopathies are an important and treatable group of disorders. The diagnostic criteria and the classifications are complex and subject to debate. Furthermore, there is clinical and histopathological overlap between the features of inflammatory myopathies and those of adult-onset genetic myopathies. In this review, we will discuss the two more common pitfalls in inflammatory myopathies diagnosis: firstly, the misdiagnosis between different types of inflammatory myopathies and uncommon myopathies; secondly, the confusion between inflammatory myopathies and genetic myopathies. Among the group of limb-girdle dystrophies, dysferlinopathies are the more common confounding myopathies. An accurate diagnosis is essential for an optimal management in patients with myopathies. (C) 2011 Societe nationale francaise de medecine interne (SNFMI). Publie par Elsevier Masson SAS. Tous droits reserves.
引用
收藏
页码：134 / 142
页数：9
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