MAGNETIC RESONANCE IMAGING PATTERN RECOGNITION IN SPORADIC INCLUSION-BODY MYOSITIS

被引:94
|
作者
Tasca, Giorgio [1 ]
Monforte, Mauro [2 ]
De Fino, Chiara [2 ]
Kley, Rudolf A. [3 ]
Ricci, Enzo [2 ]
Mirabella, Massimiliano [2 ]
机构
[1] Don Carlo Gnocchi ONLUS Fdn, Milan, Italy
[2] Univ Cattolica Sacro Cuore, Sch Med, Inst Neurol, I-00168 Rome, Italy
[3] Ruhr Univ Bochum, Dept Neurol, Univ Hosp Bergmannsheil, Bochum, Germany
关键词
MUSCULAR-DYSTROPHY; SKELETAL-MUSCLES; DIAGNOSIS; MYOPATHIES; MRI;
D O I
10.1002/mus.24661
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: In sporadic inclusion-body myositis (IBM), additional tools are needed to confirm the diagnosis, particularly in clinically atypical or pathologically unproven patients. The aims of this study were to define the pattern of muscle MRI in IBM and to assess its accuracy in differentiating IBM from other myopathies that overlap with it clinically or pathologically. Methods: Blind assessment was done on the scans of 17 definite IBM, 2 possible IBM, and 118 patients with other myopathies. Results: The diagnostic accuracy to detect definite IBM was 95% for the typical pattern (with 100% specificity) and 97% for both typical and consistent patterns (with 97% specificity). Conclusions: Muscle MRI is an accurate tool for diagnostic work-up of suspected IBM patients and may be particularly helpful in patients with early disease or who lack the classical IBM pathology.
引用
收藏
页码:956 / 962
页数:7
相关论文
共 50 条
  • [21] Pilot trial of simvastatin in the treatment of sporadic inclusion-body myositis
    Sancricca, Cristina
    Mora, Marina
    Ricci, Enzo
    Tonali, Pietro Attilio
    Mantegazza, Renato
    Mirabella, Massimiliano
    NEUROLOGICAL SCIENCES, 2011, 32 (05) : 841 - 847
  • [22] Mitochondrial DNA abnormalities and the pathogenesis of sporadic inclusion-body myositis
    Horvath, R
    Fu, K
    Genge, A
    Karpati, G
    Shoubridge, EA
    NEUROLOGY, 1996, 46 (02) : 1007 - 1007
  • [23] Difference in expression of phosphorylated tau epitopes between sporadic inclusion-body myositis and hereditary inclusion-body myopathies
    Mirabella, M
    Alvarez, RB
    Bilak, M
    Engel, WK
    Askanas, V
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1996, 55 (07): : 774 - 786
  • [24] Multiparametric Cardiac Magnetic Resonance Imaging of Cardiac Involvement Associated With Sporadic Inclusion Body Myositis
    Hayashi, Hidetaka
    Oda, Seitaro
    Kidoh, Masafumi
    Jyo, Aki
    Kobayashi, Naoki
    Okada, Yujiro
    Matsubara, Soichiro
    Ueda, Mitsuharu
    Hirai, Toshinori
    CIRCULATION-CARDIOVASCULAR IMAGING, 2021, 14 (12) : 1155 - 1156
  • [25] Association between muscle strength, histopathology, and magnetic resonance imaging in sporadic inclusion body myositis
    Dahlbom, Kathe
    Geijer, Mats
    Oldfors, Anders
    Lindberg, Christopher
    ACTA NEUROLOGICA SCANDINAVICA, 2019, 139 (02): : 177 - 182
  • [26] A perspective on sporadic inclusion-body myositis - The role of aging and inflammatory processes
    Finch, CE
    NEUROLOGY, 2006, 66 : S1 - S6
  • [27] Neurodegeneration-associated proteins and inflammation in sporadic inclusion-body myositis
    Lampe, JB
    Walter, MC
    Reichmann, H
    NEUROPATHOLOGY AND GENETICS OF DEMENTIA, 2001, 487 : 219 - 228
  • [28] Upregulation of antioxidative enzyme peroxiredoxin 5 in sporadic inclusion-body myositis
    Yang, F
    Wang, M
    Wei, A
    Knoops, B
    Ouvrier, R
    Pollard, J
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2002, 199 : S51 - S51
  • [29] Increased aging in primary muscle cultures of sporadic inclusion-body myositis
    Morosetti, Roberta
    Broccolini, Aldobrando
    Sancricca, Cristina
    Gliubizzi, Carla
    Gidaro, Teresa
    Tonali, Pietro A.
    Ricci, Enzo
    Mirabella, Massimiliano
    NEUROBIOLOGY OF AGING, 2010, 31 (07) : 1205 - 1214
  • [30] Sporadic inclusion-body myositis: Recent advances and the state of the art in 2016
    Gallay, L.
    Petiot, P.
    REVUE NEUROLOGIQUE, 2016, 172 (10) : 581 - 586