Inclusion Body Myositis

被引：73

作者：

Dimachkie, Mazen M. ^{[1
]}

Barohn, Richard J. ^{[2
]}

机构：

[1] Univ Kansas, Med Ctr, Dept Neurol, Neurophysiol Div,Neuromuscular Sect, Kansas City, KS 66160 USA

[2] Univ Kansas, Med Ctr, Dept Neurol, Kansas City, KS 66160 USA

来源：

NEUROLOGIC CLINICS | 2014年 / 32卷 / 03期

关键词：

Inclusion body myositis; Idiopathic inflammatory myopathies; Polymyositis; Diagnosis; Pathology; Pathophysiology; Treatment; Prognosis; CYTOSOLIC 5'-NUCLEOTIDASE 1A; QUANTITATIVE ASSESSMENT; PILOT TRIAL; CLINICAL-COURSE; MUSCLE; BETA; EPIDEMIOLOGY; EXPLANATION; PREVALENCE; DISEASE;

D O I：

10.1016/j.ncl.2014.04.001

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

The idiopathic inflammatory myopathies (IIMs) are a heterogenous group of rare disorders that share many similarities. In addition to sporadic inclusion body myositis (IBM), these include dermatomyositis, polymyositis, and autoimmune necrotizing myopathy. IBM is the most common IIM after age 50 years. Muscle histopathology shows endomysial inflammatory exudates surrounding and invading nonnecrotic muscle fibers often accompanied by rimmed vacuoles and protein deposits. It is likely that IBM has a prominent degenerative component. This article reviews the evolution of knowledge in IBM, with emphasis on recent developments in the field, and discusses ongoing clinical trials.

引用

页码：629 / +

页数：19

共 50 条

[31] Treatment for inclusion body myositis
Rose, Michael R.
Jones, Katherine
Leong, Kevin
Walter, Maggie C.
Miller, James
Dalakas, Marinos C.
Brassington, Ruth
Griggs, Robert
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2015, (06):
[32] INCLUSION BODY MYOSITIS - REPLY
NEVILLE, HE
RINGEL, SP
SUJANSKY, E
BAUMBACH, LL
RUSSO, LP
GARCIA, C
NEUROLOGY, 1992, 42 (11) : 2232 - 2232
[33] Inclusion body myositis: update
Lahouti, Arash H.
Amato, Anthony A.
Christopher-Stine, Lisa
CURRENT OPINION IN RHEUMATOLOGY, 2014, 26 (06) : 690 - 696
[34] SPECTRUM OF INCLUSION BODY MYOSITIS
RINGEL, S
KENNY, C
NEVILLE, H
GILDEN, D
MUSCLE & NERVE, 1986, 9 (05) : 218 - 218
[35] DYSPHAGIA IN INCLUSION BODY MYOSITIS
WINTZEN, AR
BOTS, GTAM
DEBAKKER, HM
HULSHOF, JH
PADBERG, GW
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1988, 51 (12): : 1542 - 1545
[36] INCLUSION BODY MYOSITIS AND PARAMYXOVIRUSES
KALLAJOKI, M
HYYPIA, T
HALONEN, P
ORVELL, C
RIMA, BK
KALIMO, H
HUMAN PATHOLOGY, 1991, 22 (01) : 29 - 32
[37] Inclusion-body myositis
Benveniste, O.
REVUE DE MEDECINE INTERNE, 2014, 35 (07): : 472 - 479
[38] Inclusion body myositis, a review
Carpenter, S
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1996, 55 (11): : 1105 - 1114
[39] Inclusion body myositis (IBM)
Gayathri, N
Anisya-Vasanth
Kumar, MV
Das, S
Santosh, V
Yasha, TC
Ramamohan, Y
Taly, AB
Gourie-Devi, M
Shankar, SK
CLINICAL NEUROPATHOLOGY, 2000, 19 (01) : 13 - 20
[40] Update on Inclusion Body Myositis
Jabari, Duaa
Vedanarayanan, V. V.
Barohn, Richard J.
Dimachkie, Mazen M.
CURRENT RHEUMATOLOGY REPORTS, 2018, 20 (08)

← 1 2 3 4 5 →