Idiopathic inflammatory myopathy / 中华神经科杂志
Chinese Journal of Neurology
; (12): 410-422,中插1, 2019.
Article
en Zh
| WPRIM
| ID: wpr-745947
Biblioteca responsable:
WPRO
ABSTRACT
Idiopathic inflammatory myopathies (IIM) are a group of acquired immune myopathy,which mainly include polymyositis,dermatomyositis,amyopathic dermatomyositis,sporadic inclusion body myosistis (sIBM) and immune-mediated necrotizing myopathy,as well as some special types of antisynthetase syndrome,anti-signal recognition particle antibody positive necrotizing myopathy (NM),anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibody positive NM.The diagnosis of these different types of IIM mainly depends on clinical manifestations,antibody detection and muscle pathological techniques.Different types of IIM have different clinical manifestations,or overlapping manifestations.This article systematically describes the evolution of IIM types,the main antibodies to myositis,the pathological characteristics of muscles,the manifestations of various types and the treatment of myositis.In addition to sIBM,patients with most of the other types of IIM have good outcomes by early diagnosis,timely,correct and adequate drug treatment.
Texto completo:
1
Índice:
WPRIM
Tipo de estudio:
Screening_studies
Idioma:
Zh
Revista:
Chinese Journal of Neurology
Año:
2019
Tipo del documento:
Article