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  • Management of inclusion body myositis - UpToDate
    INTRODUCTION Sporadic inclusion body myositis (IBM) is classified along with polymyositis, dermatomyositis, and autoimmune necrotizing myopathy as one of the idiopathic inflammatory myopathies
  • Management of inclusion body myositis - UpToDate
    INTRODUCTION Sporadic inclusion body myositis (IBM) is classified along with polymyositis, dermatomyositis, and autoimmune necrotizing myopathy as one of the idiopathic inflammatory myopathies
  • Diagnostic approach to patients with suspected muscle disorders . . .
    INTRODUCTION AND TERMINOLOGY Muscle disorders encompass a clinically heterogeneous group of primary diseases affecting skeletal muscle with varying degrees of extramuscular involvement These conditions are commonly referred to as myopathies Myositis, or inflammatory myopathy, typically describes a group of immune-mediated myopathies that classically show prominent inflammatory cell
  • Diagnosis and differential diagnosis of dermatomyositis and . . . - UpToDate
    The pathogenesis, clinical manifestations, and treatment of these diseases and of the related disorders that occur in children (known as juvenile DM and PM); malignancy in patients with DM and PM; and the clinical manifestations, diagnosis, and treatment of inclusion body myositis (IBM) are discussed separately
  • 包涵体肌炎的处理 - UpToDate
    引言 散发性包涵体肌炎 (inclusion body myositis, IBM)与多发性肌炎、皮肌炎和自身免疫性坏死性肌病一起归为特发性炎性肌病。然而，尽管组织学上有相似之处，但IBM的临床病理表现、治疗和预后与其他疾病明显不同 (表 1)。 (参见 “成人皮肌炎与多发性肌炎的临床表现” 和 “成人皮肌炎和多发性肌炎的
  • 特发性炎性肌病的概述 - UpToDate
    引言 特发性炎性肌病 (idiopathic inflammatory myopathy, IIM)包括皮肌炎 (dermatomyositis, DM)、多发性肌炎 (polymyositis, PM)、风湿病重叠综合征肌炎、抗合成酶综合征肌炎、免疫介导的坏死性肌病 (immune-mediated necrotizing myopathy, IMNM)及包涵体肌炎 (inclusion body myositis, IBM)。这些疾病的临床表现为进行性肌无力，组织
  • Clinical manifestations of dermatomyositis and polymyositis . . . - UpToDate
    The three other major immune-mediated myopathies are antisynthetase syndrome, immune-mediated necrotizing myopathy (IMNM), and inclusion body myositis (IBM) IMNM shares clinical findings and some serologic markers with DM and PM, while both IMNM and IBM have histopathologic findings on muscle biopsy that distinguish them from DM and PM
  • Overview of and approach to the idiopathic inflammatory myopathies
    INTRODUCTION The idiopathic inflammatory myopathies (IIMs) include dermatomyositis (DM), myositis of the antisynthetase syndrome, immune-mediated necrotizing myopathy (IMNM), inclusion body myositis (IBM), and myositis as part of a rheumatic disease overlap syndrome
  • 包涵体肌炎的处理 - UpToDate
    引言 散发性包涵体肌炎 (inclusion body myositis, IBM)与多发性肌炎、皮肌炎和自身免疫性坏死性肌病一起归为特发性炎性肌病。然而，尽管组织学上有相似之处，但IBM的临床病理表现、治疗和预后与其他疾病明显不同 (表 1)。 (参见 “成人皮肌炎与多发性肌炎的临床表现” 和 “成人皮肌炎和多发性肌炎的
  • Diagnosis and differential diagnosis of dermatomyositis and . . . - UpToDate
    Inclusion body myositis – Inclusion body myositis (IBM) is the inflammatory myopathy most commonly misdiagnosed as PM, and, in cases of "refractory PM," the correct diagnosis often proves to be IBM In contrast to PM, IBM generally has a more insidious onset, asymmetric weakness, and more prominent forearm muscles (table 2)





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