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Published in: Skeletal Radiology 5/2019

01-05-2019 | Review Article

Whole-body MRI and pathological findings in adult patients with myopathies

Authors: Xavier Tomas, Jose Cesar Milisenda, Ana Isabel Garcia-Diez, Sergio Prieto-Gonzalez, Marie Faruch, Jaime Pomes, Josep Maria Grau-Junyent

Published in: Skeletal Radiology | Issue 5/2019

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Abstract

Magnetic resonance imaging (MRI) is considered the most sensitive and specific imaging technique for the detection of muscle diseases related to myopathies. Since 2008, the use of whole-body MRI (WBMRI) to evaluate myopathies has improved due to technical advances such as rolling table platform and parallel imaging, which enable rapid assessment of the entire musculoskeletal system with high-quality images. WBMRI protocols should include T1-weighted and short-tau inversion recovery (STIR), which provide the basic pulse sequences for studying myopathies, in order to detect fatty infiltration/muscle atrophy and muscle edema, respectively. High signal intensity in T1-weighted images shows chronic disease with fatty infiltration, whereas high signal intensity in STIR indicates an acute stage with muscle edema. Additional sequences such as diffusion-weighted imaging (DWI) can be readily incorporated into routine WBMRI study protocols. Contrast-enhanced sequences have not been done. This article reviews WBMRI as an imaging method to evaluate different myopathies (idiopathic inflammatory, dystrophic, non-dystrophic, metabolic, and channelopathies). WBMRI provides a comprehensive estimate of the total burden with a single study, seeking specific distribution patterns, including clinically silent involvement of muscle areas. Furthermore, WBMRI may help to select the “target muscle area” for biopsy during patient follow-up. It may be also be used to detect related and non-related pathological conditions, such as tumors.
Literature
1.
go back to reference Findlay AR, Goyal NA, Mozaffar T. An overview of polymyositis and dermatomyositis. Muscle Nerve. 2015;51(5):638–56.CrossRefPubMed Findlay AR, Goyal NA, Mozaffar T. An overview of polymyositis and dermatomyositis. Muscle Nerve. 2015;51(5):638–56.CrossRefPubMed
3.
go back to reference Pipitone N. Value of MRI in diagnostics and evaluation of myositis. Curr Opin Rheumatol. 2016;28(6):625–30.CrossRefPubMed Pipitone N. Value of MRI in diagnostics and evaluation of myositis. Curr Opin Rheumatol. 2016;28(6):625–30.CrossRefPubMed
4.
go back to reference Curiel RV, Jones R, Brindle K. Magnetic resonance imaging of the idiopathic inflammatory myopathies: structural and clinical aspects. Ann N Y Acad Sci. 2009;1154:101–14.CrossRefPubMed Curiel RV, Jones R, Brindle K. Magnetic resonance imaging of the idiopathic inflammatory myopathies: structural and clinical aspects. Ann N Y Acad Sci. 2009;1154:101–14.CrossRefPubMed
5.
go back to reference Schmidt GP, Reiser MF, Baur-Melnyk A. Whole-body imaging of the musculoskeletal system: the value of MR imaging. Skelet Radiol. 2007;36(12):1109–19.CrossRef Schmidt GP, Reiser MF, Baur-Melnyk A. Whole-body imaging of the musculoskeletal system: the value of MR imaging. Skelet Radiol. 2007;36(12):1109–19.CrossRef
6.
go back to reference Filli L, Maurer B, Manoliu A, Andreisek G, Guggenberger R. Whole-body MRI in adult inflammatory myopathies: do we need imaging of the trunk? Eur Radiol. 2015;25(12):3499–07.CrossRefPubMed Filli L, Maurer B, Manoliu A, Andreisek G, Guggenberger R. Whole-body MRI in adult inflammatory myopathies: do we need imaging of the trunk? Eur Radiol. 2015;25(12):3499–07.CrossRefPubMed
7.
go back to reference Del Grande F, Carrino JA, Del Grande M, Mammen AL, Christopher Stine L. Magnetic resonance imaging of inflammatory myopathies. Top Magn Reson Imaging. 2011;22(2):39–43.CrossRefPubMed Del Grande F, Carrino JA, Del Grande M, Mammen AL, Christopher Stine L. Magnetic resonance imaging of inflammatory myopathies. Top Magn Reson Imaging. 2011;22(2):39–43.CrossRefPubMed
8.
go back to reference Yao L, Yip AL, Shrader JA, et al. Magnetic resonance measurement of muscle T2, fat-corrected T2 and fat fraction in the assessment of idiopathic inflammatory myopathies. Rheumatology (Oxford). 2016;55(3):441–9. Yao L, Yip AL, Shrader JA, et al. Magnetic resonance measurement of muscle T2, fat-corrected T2 and fat fraction in the assessment of idiopathic inflammatory myopathies. Rheumatology (Oxford). 2016;55(3):441–9.
9.
go back to reference Zaidman C, Hobson-Webb L. Imaging of skeletal muscle in neuromuscular disease: a clinical perspective. In: Weber MA, editor. Magnetic resonance imaging of the skeletal musculature. Berlin: Springer-Verlag; 2013. p. 3–22.CrossRef Zaidman C, Hobson-Webb L. Imaging of skeletal muscle in neuromuscular disease: a clinical perspective. In: Weber MA, editor. Magnetic resonance imaging of the skeletal musculature. Berlin: Springer-Verlag; 2013. p. 3–22.CrossRef
10.
go back to reference Dobloug C, Garen T, Bitter H, et al. Prevalence and clinical characteristics of adult polymyositis and dermatomyositis; data from a large and unselected Norwegian cohort. Ann Rheum Dis. 2015;74(8):1551–6.CrossRefPubMed Dobloug C, Garen T, Bitter H, et al. Prevalence and clinical characteristics of adult polymyositis and dermatomyositis; data from a large and unselected Norwegian cohort. Ann Rheum Dis. 2015;74(8):1551–6.CrossRefPubMed
11.
go back to reference Van De Vlekkert J, Maas M, Hoogendijk JE, De Visser M, Van Schaik IN. Combining MRI and muscle biopsy improves diagnostic accuracy in subacute-onset idiopathic inflammatory myopathy. Muscle Nerve. 2015;51(2):253–8.CrossRef Van De Vlekkert J, Maas M, Hoogendijk JE, De Visser M, Van Schaik IN. Combining MRI and muscle biopsy improves diagnostic accuracy in subacute-onset idiopathic inflammatory myopathy. Muscle Nerve. 2015;51(2):253–8.CrossRef
12.
go back to reference McCann LJ, Juggins AD, Maillard SM, et al. The juvenile dermatomyositis national registry and repository (UK and Ireland)—clinical characteristics of children recruited within the first 5 years. Rheumatology (Oxford). 2006;45(10):1255–60.CrossRef McCann LJ, Juggins AD, Maillard SM, et al. The juvenile dermatomyositis national registry and repository (UK and Ireland)—clinical characteristics of children recruited within the first 5 years. Rheumatology (Oxford). 2006;45(10):1255–60.CrossRef
13.
go back to reference Gowdie PJ, Allen RC, Kornberg AJ, Akikusa JD. Clinical features and disease course of patients with juvenile dermatomyositis. Int J Rheum Dis. 2013;16(5):561–7.CrossRefPubMed Gowdie PJ, Allen RC, Kornberg AJ, Akikusa JD. Clinical features and disease course of patients with juvenile dermatomyositis. Int J Rheum Dis. 2013;16(5):561–7.CrossRefPubMed
14.
go back to reference Maurer B, Walker UA. Role of MRI in diagnosis and management of idiopathic inflammatory myopathies. Curr Rheumatol Rep. 2015;17(11):67.CrossRefPubMed Maurer B, Walker UA. Role of MRI in diagnosis and management of idiopathic inflammatory myopathies. Curr Rheumatol Rep. 2015;17(11):67.CrossRefPubMed
15.
go back to reference Day J, Patel S, Limaye V. The role of magnetic resonance imaging techniques in evaluation and management of the idiopathic inflammatory myopathies. Semin Arthritis Rheum. 2017;46(5):642–9.CrossRefPubMed Day J, Patel S, Limaye V. The role of magnetic resonance imaging techniques in evaluation and management of the idiopathic inflammatory myopathies. Semin Arthritis Rheum. 2017;46(5):642–9.CrossRefPubMed
17.
go back to reference Malattia C, Damasio MB, Madeo A, et al. Whole-body MRI in the assessment of disease activity in juvenile dermatomyositis. Ann Rheum Dis. 2014;73(6):1083–90.CrossRefPubMed Malattia C, Damasio MB, Madeo A, et al. Whole-body MRI in the assessment of disease activity in juvenile dermatomyositis. Ann Rheum Dis. 2014;73(6):1083–90.CrossRefPubMed
18.
go back to reference Barsotti S, Zampa V, Talarico R, et al. Thigh magnetic resonance imaging for the evaluation of disease activity in patients with idiopathic inflammatory myopathies followed in a single center. Muscle Nerve. 2016;54(4):666–72.CrossRefPubMed Barsotti S, Zampa V, Talarico R, et al. Thigh magnetic resonance imaging for the evaluation of disease activity in patients with idiopathic inflammatory myopathies followed in a single center. Muscle Nerve. 2016;54(4):666–72.CrossRefPubMed
19.
go back to reference Linklater H, Pipitone N, Rose MR, et al. Classifying idiopathic inflammatory myopathies: comparing the performance of six existing criteria. Clin Exp Rheumatol. 2013;31(5):767–9.PubMed Linklater H, Pipitone N, Rose MR, et al. Classifying idiopathic inflammatory myopathies: comparing the performance of six existing criteria. Clin Exp Rheumatol. 2013;31(5):767–9.PubMed
20.
21.
go back to reference Hoogendijk JE, Amato AA, Lecky BR, Choy EH, Lundberg IE, Rose MR, et al. 119th ENMC international workshop: trial design in adult idiopathic inflammatory myopathies, with the exception of inclusion body myositis, 10-12 October 2003, Naarden, The Netherlands. Neuromuscular disorders : NMD. England; 2004. p. 337–45. Hoogendijk JE, Amato AA, Lecky BR, Choy EH, Lundberg IE, Rose MR, et al. 119th ENMC international workshop: trial design in adult idiopathic inflammatory myopathies, with the exception of inclusion body myositis, 10-12 October 2003, Naarden, The Netherlands. Neuromuscular disorders : NMD. England; 2004. p. 337–45.
22.
go back to reference Kubínová K, Mann H, Vencovský J. MRI scoring methods used in evaluation of muscle involvement in patients with idiopathic inflammatory myopathies. Curr Opin Rheumatol. 2017;29(6):623–31.PubMed Kubínová K, Mann H, Vencovský J. MRI scoring methods used in evaluation of muscle involvement in patients with idiopathic inflammatory myopathies. Curr Opin Rheumatol. 2017;29(6):623–31.PubMed
23.
go back to reference Dallaudière B, Lecouvet F, Vande Berg B, et al. Diffusion-weighted MR imaging in musculoskeletal diseases: current concepts. Diagn Interv Imaging. 2015;96(4):327–40.CrossRefPubMed Dallaudière B, Lecouvet F, Vande Berg B, et al. Diffusion-weighted MR imaging in musculoskeletal diseases: current concepts. Diagn Interv Imaging. 2015;96(4):327–40.CrossRefPubMed
24.
25.
go back to reference Qi J, Olsen NJ, Price RR, Winston JA, Park JH. Diffusion-weighted imaging of inflammatory myopathies: polymyositis and dermatomyositis. J Magn Reson Imaging. 2008;27(1):212–7.CrossRefPubMed Qi J, Olsen NJ, Price RR, Winston JA, Park JH. Diffusion-weighted imaging of inflammatory myopathies: polymyositis and dermatomyositis. J Magn Reson Imaging. 2008;27(1):212–7.CrossRefPubMed
26.
go back to reference Ai T, Yu K, Gao L, et al. Diffusion tensor imaging in evaluation of thigh muscles in patients with polymyositis and dermatomyositis. Br J Radiol. 2014;87(1043):20140261.CrossRefPubMedPubMedCentral Ai T, Yu K, Gao L, et al. Diffusion tensor imaging in evaluation of thigh muscles in patients with polymyositis and dermatomyositis. Br J Radiol. 2014;87(1043):20140261.CrossRefPubMedPubMedCentral
27.
go back to reference Hill CL, Zhang Y, Sigurgeirsson B, et al. Frequency of specific cancer types in dermatomyositis and polymyositis: a population-based study. Lancet. 2001;357(9250):96–100.CrossRefPubMed Hill CL, Zhang Y, Sigurgeirsson B, et al. Frequency of specific cancer types in dermatomyositis and polymyositis: a population-based study. Lancet. 2001;357(9250):96–100.CrossRefPubMed
28.
go back to reference Chen Y-J, Wu C-Y, Huang Y-L, Wang C-B, Shen J-L, Chang Y-T. Cancer risks of dermatomyositis and polymyositis: a nationwide cohort study in Taiwan. Arthritis Res Ther. 2010;12(2):R70.CrossRefPubMedPubMedCentral Chen Y-J, Wu C-Y, Huang Y-L, Wang C-B, Shen J-L, Chang Y-T. Cancer risks of dermatomyositis and polymyositis: a nationwide cohort study in Taiwan. Arthritis Res Ther. 2010;12(2):R70.CrossRefPubMedPubMedCentral
29.
go back to reference Garcia J. MRI in inflammatory myopathies. Skelet Radiol. 2000;29(8):425–38.CrossRef Garcia J. MRI in inflammatory myopathies. Skelet Radiol. 2000;29(8):425–38.CrossRef
30.
go back to reference O’Connell MJ, Powell T, Brennan D, Lynch T, McCarthy CJ, Eustace SJ. Whole-body MR imaging in the diagnosis of polymyositis. AJR Am J Roentgenol. 2002;179(4):967–71.CrossRefPubMed O’Connell MJ, Powell T, Brennan D, Lynch T, McCarthy CJ, Eustace SJ. Whole-body MR imaging in the diagnosis of polymyositis. AJR Am J Roentgenol. 2002;179(4):967–71.CrossRefPubMed
31.
go back to reference Harris-Love MO, Shrader JA, Koziol D, et al. Distribution and severity of weakness among patients with polymyositis, dermatomyositis and juvenile dermatomyositis. Rheumatology (Oxford). 2009;48(2):134–9.CrossRef Harris-Love MO, Shrader JA, Koziol D, et al. Distribution and severity of weakness among patients with polymyositis, dermatomyositis and juvenile dermatomyositis. Rheumatology (Oxford). 2009;48(2):134–9.CrossRef
32.
go back to reference Cantwell C, Ryan M, O’Connell M, et al. A comparison of inflammatory myopathies at whole-body turbo STIR MRI. Clin Radiol. 2005;60(2):261–7.CrossRefPubMed Cantwell C, Ryan M, O’Connell M, et al. A comparison of inflammatory myopathies at whole-body turbo STIR MRI. Clin Radiol. 2005;60(2):261–7.CrossRefPubMed
34.
go back to reference Dion E, Cherin P, Payan C, et al. Magnetic resonance imaging criteria for distinguishing between inclusion body myositis and polymyositis. J Rheumatol. 2002;29(9):1897–06.PubMed Dion E, Cherin P, Payan C, et al. Magnetic resonance imaging criteria for distinguishing between inclusion body myositis and polymyositis. J Rheumatol. 2002;29(9):1897–06.PubMed
35.
go back to reference Zheng Y, Liu L, Wang L, et al. Magnetic resonance imaging changes of thigh muscles in myopathy with antibodies to signal recognition particle. Rheumatology (Oxford). 2015;54(6):1017–24.CrossRef Zheng Y, Liu L, Wang L, et al. Magnetic resonance imaging changes of thigh muscles in myopathy with antibodies to signal recognition particle. Rheumatology (Oxford). 2015;54(6):1017–24.CrossRef
36.
go back to reference Luo Y-B, Mastaglia FL. Dermatomyositis, polymyositis and immune-mediated necrotising myopathies. Biochim Biophys Acta. 2015;1852(4):622–32.CrossRefPubMed Luo Y-B, Mastaglia FL. Dermatomyositis, polymyositis and immune-mediated necrotising myopathies. Biochim Biophys Acta. 2015;1852(4):622–32.CrossRefPubMed
37.
go back to reference Badrising UA, Maat-Schieman M, van Duinen SG, et al. Epidemiology of inclusion body myositis in the Netherlands: a nationwide study. Neurology. 2000;55(9):1385–7.CrossRefPubMed Badrising UA, Maat-Schieman M, van Duinen SG, et al. Epidemiology of inclusion body myositis in the Netherlands: a nationwide study. Neurology. 2000;55(9):1385–7.CrossRefPubMed
38.
go back to reference Wilson FC, Ytterberg SR, St Sauver JL, Reed AM. Epidemiology of sporadic inclusion body myositis and polymyositis in Olmsted County, Minnesota. J Rheumatol. 2008;35(3):445–7.PubMed Wilson FC, Ytterberg SR, St Sauver JL, Reed AM. Epidemiology of sporadic inclusion body myositis and polymyositis in Olmsted County, Minnesota. J Rheumatol. 2008;35(3):445–7.PubMed
39.
go back to reference Askanas V, Engel WK, Nogalska A. Sporadic inclusion-body myositis: a degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagy. Biochim Biophys Acta. 2015;1852(4):633–43.CrossRefPubMed Askanas V, Engel WK, Nogalska A. Sporadic inclusion-body myositis: a degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagy. Biochim Biophys Acta. 2015;1852(4):633–43.CrossRefPubMed
40.
go back to reference Needham M, Mastaglia FL. Inclusion body myositis: current pathogenetic concepts and diagnostic and therapeutic approaches. Lancet Neurol. 2007;6(7):620–31.CrossRefPubMed Needham M, Mastaglia FL. Inclusion body myositis: current pathogenetic concepts and diagnostic and therapeutic approaches. Lancet Neurol. 2007;6(7):620–31.CrossRefPubMed
41.
go back to reference Cox FM, Titulaer MJ, Sont JK, Wintzen AR, Verschuuren JJGM, Badrising UA. A 12-year follow-up in sporadic inclusion body myositis: an end stage with major disabilities. Brain. 2011;134(Pt 11):3167–75.CrossRefPubMed Cox FM, Titulaer MJ, Sont JK, Wintzen AR, Verschuuren JJGM, Badrising UA. A 12-year follow-up in sporadic inclusion body myositis: an end stage with major disabilities. Brain. 2011;134(Pt 11):3167–75.CrossRefPubMed
42.
go back to reference Kissel JT. Misunderstandings, misperceptions, and mistakes in the management of the inflammatory myopathies. Semin Neurol. 2002;22(1):41–51.CrossRefPubMed Kissel JT. Misunderstandings, misperceptions, and mistakes in the management of the inflammatory myopathies. Semin Neurol. 2002;22(1):41–51.CrossRefPubMed
43.
go back to reference Cox FM, Reijnierse M, van Rijswijk CSP, Wintzen AR, Verschuuren JJ, Badrising UA. Magnetic resonance imaging of skeletal muscles in sporadic inclusion body myositis. Rheumatology (Oxford). 2011;50(6):1153–61.CrossRef Cox FM, Reijnierse M, van Rijswijk CSP, Wintzen AR, Verschuuren JJ, Badrising UA. Magnetic resonance imaging of skeletal muscles in sporadic inclusion body myositis. Rheumatology (Oxford). 2011;50(6):1153–61.CrossRef
44.
go back to reference Tasca G, Monforte M, De Fino C, Kley RA, Ricci E, Mirabella M. Magnetic resonance imaging pattern recognition in sporadic inclusion-body myositis. Muscle Nerve. 2015;52(6):956–62.CrossRefPubMed Tasca G, Monforte M, De Fino C, Kley RA, Ricci E, Mirabella M. Magnetic resonance imaging pattern recognition in sporadic inclusion-body myositis. Muscle Nerve. 2015;52(6):956–62.CrossRefPubMed
45.
go back to reference van der Meulen MFG, Bronner IM, Hoogendijk JE, Burger H, van Venrooij WJ, Voskuyl AE, et al. Polymyositis: an overdiagnosed entity. Neurology. 2003;61(3):316–21.CrossRefPubMed van der Meulen MFG, Bronner IM, Hoogendijk JE, Burger H, van Venrooij WJ, Voskuyl AE, et al. Polymyositis: an overdiagnosed entity. Neurology. 2003;61(3):316–21.CrossRefPubMed
46.
go back to reference Stenzel W, Goebel H-H, Aronica E. Review: immune-mediated necrotizing myopathies—a heterogeneous group of diseases with specific myopathological features. Neuropathol Appl Neurobiol. 2012;38(7):632–46.CrossRefPubMed Stenzel W, Goebel H-H, Aronica E. Review: immune-mediated necrotizing myopathies—a heterogeneous group of diseases with specific myopathological features. Neuropathol Appl Neurobiol. 2012;38(7):632–46.CrossRefPubMed
47.
go back to reference Mammen AL, Chung T, Christopher-Stine L, et al. Autoantibodies against 3-hydroxy-3-methylglutaryl-coenzyme a reductase in patients with statin-associated autoimmune myopathy. Arthritis Rheum. 2011;63(3):713–21.CrossRefPubMedPubMedCentral Mammen AL, Chung T, Christopher-Stine L, et al. Autoantibodies against 3-hydroxy-3-methylglutaryl-coenzyme a reductase in patients with statin-associated autoimmune myopathy. Arthritis Rheum. 2011;63(3):713–21.CrossRefPubMedPubMedCentral
48.
49.
go back to reference Ernste FC, Reed AM. Idiopathic inflammatory myopathies: current trends in pathogenesis, clinical features, and up-to-date treatment recommendations. Mayo Clin Proc. 2013;88(1):83–105.CrossRefPubMed Ernste FC, Reed AM. Idiopathic inflammatory myopathies: current trends in pathogenesis, clinical features, and up-to-date treatment recommendations. Mayo Clin Proc. 2013;88(1):83–105.CrossRefPubMed
50.
go back to reference Pinal-Fernandez I, Casal-Dominguez M, Carrino JA, et al. Thigh muscle MRI in immune-mediated necrotising myopathy: extensive oedema, early muscle damage and role of anti-SRP autoantibodies as a marker of severity. Ann Rheum Dis. 2017;76(4):681–7.CrossRefPubMed Pinal-Fernandez I, Casal-Dominguez M, Carrino JA, et al. Thigh muscle MRI in immune-mediated necrotising myopathy: extensive oedema, early muscle damage and role of anti-SRP autoantibodies as a marker of severity. Ann Rheum Dis. 2017;76(4):681–7.CrossRefPubMed
51.
go back to reference Low AHL, Lax M, Johnson SR, Lee P. Magnetic resonance imaging of the hand in systemic sclerosis. J Rheumatol. 2009;36(5):961–4.CrossRefPubMed Low AHL, Lax M, Johnson SR, Lee P. Magnetic resonance imaging of the hand in systemic sclerosis. J Rheumatol. 2009;36(5):961–4.CrossRefPubMed
52.
go back to reference Schanz S, Henes J, Ulmer A, et al. Magnetic resonance imaging findings in patients with systemic scleroderma and musculoskeletal symptoms. Eur Radiol. 2013;23(1):212–21.CrossRefPubMed Schanz S, Henes J, Ulmer A, et al. Magnetic resonance imaging findings in patients with systemic scleroderma and musculoskeletal symptoms. Eur Radiol. 2013;23(1):212–21.CrossRefPubMed
53.
go back to reference Schanz S, Fierlbeck G, Ulmer A, et al. Localized scleroderma: MR findings and clinical features. Radiology. 2011;260(3):817–24.CrossRefPubMed Schanz S, Fierlbeck G, Ulmer A, et al. Localized scleroderma: MR findings and clinical features. Radiology. 2011;260(3):817–24.CrossRefPubMed
54.
go back to reference Whitlock JB, Dimberg EL, Selcen D, Rubin DI. Eosinophilic fasciitis with subjacent myositis. Muscle Nerve. 2017;56(3):525–9.CrossRefPubMed Whitlock JB, Dimberg EL, Selcen D, Rubin DI. Eosinophilic fasciitis with subjacent myositis. Muscle Nerve. 2017;56(3):525–9.CrossRefPubMed
55.
56.
go back to reference Mazori DR, Femia AN, Vleugels RA. Eosinophilic fasciitis: an updated review on diagnosis and treatment. Curr Rheumatol Rep. 2017;19(12):74.CrossRefPubMed Mazori DR, Femia AN, Vleugels RA. Eosinophilic fasciitis: an updated review on diagnosis and treatment. Curr Rheumatol Rep. 2017;19(12):74.CrossRefPubMed
58.
go back to reference Chaudhry AA, Baker KS, Gould ES, Gupta R. Necrotizing fasciitis and its mimics: what radiologists need to know. AJR Am J Roentgenol. 2015;204(1):128–39.CrossRefPubMed Chaudhry AA, Baker KS, Gould ES, Gupta R. Necrotizing fasciitis and its mimics: what radiologists need to know. AJR Am J Roentgenol. 2015;204(1):128–39.CrossRefPubMed
59.
go back to reference Finanger EL, Russman B, Forbes SC, Rooney WD, Walter GA, Vandenborne K. Use of skeletal muscle MRI in diagnosis and monitoring disease progression in Duchenne muscular dystrophy. Phys Med Rehabil Clin N Am. 2012;23(1):1–10 ix.CrossRefPubMed Finanger EL, Russman B, Forbes SC, Rooney WD, Walter GA, Vandenborne K. Use of skeletal muscle MRI in diagnosis and monitoring disease progression in Duchenne muscular dystrophy. Phys Med Rehabil Clin N Am. 2012;23(1):1–10 ix.CrossRefPubMed
60.
go back to reference Tasca G, Iannaccone E, Monforte M, et al. Muscle MRI in Becker muscular dystrophy. Neuromuscul Disord. 2012;22(Suppl 2):S100–6.CrossRefPubMed Tasca G, Iannaccone E, Monforte M, et al. Muscle MRI in Becker muscular dystrophy. Neuromuscul Disord. 2012;22(Suppl 2):S100–6.CrossRefPubMed
61.
go back to reference Sookhoo S, Mackinnon I, Bushby K, Chinnery PF, Birchall D. MRI for the demonstration of subclinical muscle involvement in muscular dystrophy. Clin Radiol. 2007;62(2):160–5.CrossRefPubMed Sookhoo S, Mackinnon I, Bushby K, Chinnery PF, Birchall D. MRI for the demonstration of subclinical muscle involvement in muscular dystrophy. Clin Radiol. 2007;62(2):160–5.CrossRefPubMed
62.
go back to reference Mercuri E, Talim B, Moghadaszadeh B, et al. Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1). Neuromuscul Disord. 2002;12(7-8):631–8.CrossRefPubMed Mercuri E, Talim B, Moghadaszadeh B, et al. Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1). Neuromuscul Disord. 2002;12(7-8):631–8.CrossRefPubMed
63.
go back to reference Marden FA, Connolly AM, Siegel MJ, Rubin DA. Compositional analysis of muscle in boys with Duchenne muscular dystrophy using MR imaging. Skelet Radiol. 2005;34(3):140–8.CrossRef Marden FA, Connolly AM, Siegel MJ, Rubin DA. Compositional analysis of muscle in boys with Duchenne muscular dystrophy using MR imaging. Skelet Radiol. 2005;34(3):140–8.CrossRef
64.
go back to reference Degardin A, Morillon D, Lacour A, Cotten A, Vermersch P, Stojkovic T. Morphologic imaging in muscular dystrophies and inflammatory myopathies. Skelet Radiol. 2010;39(12):1219–27.CrossRef Degardin A, Morillon D, Lacour A, Cotten A, Vermersch P, Stojkovic T. Morphologic imaging in muscular dystrophies and inflammatory myopathies. Skelet Radiol. 2010;39(12):1219–27.CrossRef
65.
go back to reference Lamminen AE. Magnetic resonance imaging of primary skeletal muscle diseases: patterns of distribution and severity of involvement. Br J Radiol. 1990;63(756):946–50.CrossRefPubMed Lamminen AE. Magnetic resonance imaging of primary skeletal muscle diseases: patterns of distribution and severity of involvement. Br J Radiol. 1990;63(756):946–50.CrossRefPubMed
66.
go back to reference Faridian-Aragh N, Wagner KR, Leung DG, Carrino JA. Magnetic resonance imaging phenotyping of Becker muscular dystrophy. Muscle Nerve. 2014;50(6):962–7.CrossRefPubMed Faridian-Aragh N, Wagner KR, Leung DG, Carrino JA. Magnetic resonance imaging phenotyping of Becker muscular dystrophy. Muscle Nerve. 2014;50(6):962–7.CrossRefPubMed
67.
go back to reference Polavarapu K, Manjunath M, Preethish-Kumar V, et al. Muscle MRI in Duchenne muscular dystrophy: evidence of a distinctive pattern. Neuromuscul Disord. 2016;26(11):768–74.CrossRefPubMed Polavarapu K, Manjunath M, Preethish-Kumar V, et al. Muscle MRI in Duchenne muscular dystrophy: evidence of a distinctive pattern. Neuromuscul Disord. 2016;26(11):768–74.CrossRefPubMed
68.
go back to reference Sugie K, Kumazawa A, Ueno S. Sporadic inclusion body myositis presenting with Beevor’s sign. Intern Med. 2015;54(21):2793–4.CrossRefPubMed Sugie K, Kumazawa A, Ueno S. Sporadic inclusion body myositis presenting with Beevor’s sign. Intern Med. 2015;54(21):2793–4.CrossRefPubMed
69.
go back to reference Milisenda JC, Rico Caballero V, García AI, Tomás X, Grau JM. "Extended" Beevor’s sing as a new clinical sign in sporadic inclusion body myositis. Med Clin (Barc). 2017;148(8):e43.CrossRef Milisenda JC, Rico Caballero V, García AI, Tomás X, Grau JM. "Extended" Beevor’s sing as a new clinical sign in sporadic inclusion body myositis. Med Clin (Barc). 2017;148(8):e43.CrossRef
70.
go back to reference Kornblum C, Lutterbey G, Bogdanow M, et al. Distinct neuromuscular phenotypes in myotonic dystrophy types 1 and 2: a whole-body highfield MRI study. J Neurol. 2006;253(6):753–61.CrossRefPubMed Kornblum C, Lutterbey G, Bogdanow M, et al. Distinct neuromuscular phenotypes in myotonic dystrophy types 1 and 2: a whole-body highfield MRI study. J Neurol. 2006;253(6):753–61.CrossRefPubMed
71.
go back to reference Kornblum C, Lutterbey GG, Czermin B, et al. Whole-body high-field MRI shows no skeletal muscle degeneration in young patients with recessive myotonia congenita. Acta Neurol Scand. 2010;121(2):131–5.CrossRefPubMed Kornblum C, Lutterbey GG, Czermin B, et al. Whole-body high-field MRI shows no skeletal muscle degeneration in young patients with recessive myotonia congenita. Acta Neurol Scand. 2010;121(2):131–5.CrossRefPubMed
72.
go back to reference Kan HE, Klomp DWJ, Wohlgemuth M, et al. Only fat infiltrated muscles in resting lower leg of FSHD patients show disturbed energy metabolism. NMR Biomed. 2010;23(6):563–8.CrossRefPubMed Kan HE, Klomp DWJ, Wohlgemuth M, et al. Only fat infiltrated muscles in resting lower leg of FSHD patients show disturbed energy metabolism. NMR Biomed. 2010;23(6):563–8.CrossRefPubMed
73.
go back to reference Kesper K, Kornblum C, Reimann J, Lutterbey G, Schröder R, Wattjes MP. Pattern of skeletal muscle involvement in primary dysferlinopathies: a whole-body 3.0-T magnetic resonance imaging study. Acta Neurol Scand. 2009;120(2):111–8.CrossRefPubMed Kesper K, Kornblum C, Reimann J, Lutterbey G, Schröder R, Wattjes MP. Pattern of skeletal muscle involvement in primary dysferlinopathies: a whole-body 3.0-T magnetic resonance imaging study. Acta Neurol Scand. 2009;120(2):111–8.CrossRefPubMed
74.
go back to reference Sarkozy A, Deschauer M, Carlier RY, et al. Muscle MRI findings in limb girdle muscular dystrophy type 2L. Neuromuscul Disord. 2012;22(Suppl 2):S122–9.CrossRefPubMed Sarkozy A, Deschauer M, Carlier RY, et al. Muscle MRI findings in limb girdle muscular dystrophy type 2L. Neuromuscul Disord. 2012;22(Suppl 2):S122–9.CrossRefPubMed
75.
go back to reference Mercuri E, Bushby K, Ricci E, et al. Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures. Neuromuscul Disord. 2005;15(2):164–71.CrossRefPubMed Mercuri E, Bushby K, Ricci E, et al. Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures. Neuromuscul Disord. 2005;15(2):164–71.CrossRefPubMed
76.
go back to reference Fischer D, Walter MC, Kesper K, et al. Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs. J Neurol. 2005;252(5):538–47.CrossRefPubMed Fischer D, Walter MC, Kesper K, et al. Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs. J Neurol. 2005;252(5):538–47.CrossRefPubMed
77.
go back to reference Bönnemann CG, Brockmann K, Hanefeld F. Muscle ultrasound in Bethlem myopathy. Neuropediatrics. 2003;34(6):335–6.CrossRefPubMed Bönnemann CG, Brockmann K, Hanefeld F. Muscle ultrasound in Bethlem myopathy. Neuropediatrics. 2003;34(6):335–6.CrossRefPubMed
78.
go back to reference Mercuri E, Lampe A, Allsop J, et al. Muscle MRI in Ullrich congenital muscular dystrophy and Bethlem myopathy. Neuromuscul Disord. 2005;15(4):303–10.CrossRefPubMed Mercuri E, Lampe A, Allsop J, et al. Muscle MRI in Ullrich congenital muscular dystrophy and Bethlem myopathy. Neuromuscul Disord. 2005;15(4):303–10.CrossRefPubMed
79.
go back to reference Filli L, Winklhofer S, Andreisek G, Del Grande F. Imaging of myopathies. Radiol Clin N Am. 2017;55(5):1055–70.CrossRefPubMed Filli L, Winklhofer S, Andreisek G, Del Grande F. Imaging of myopathies. Radiol Clin N Am. 2017;55(5):1055–70.CrossRefPubMed
80.
go back to reference Fischer D, Wattjes MP. MRI in muscle dystrophies and primary myopathies. In: Weber MA, editor. Magnetic resonance imaging of the skeletal musculature. Berlin: Springer-Verlag; 2013. p. 241–4.CrossRef Fischer D, Wattjes MP. MRI in muscle dystrophies and primary myopathies. In: Weber MA, editor. Magnetic resonance imaging of the skeletal musculature. Berlin: Springer-Verlag; 2013. p. 241–4.CrossRef
81.
go back to reference Quijano-Roy S, Carlier RY, Fischer D. Muscle imaging in congenital myopathies. Semin Pediatr Neurol. 2011;18(4):221–9.CrossRefPubMed Quijano-Roy S, Carlier RY, Fischer D. Muscle imaging in congenital myopathies. Semin Pediatr Neurol. 2011;18(4):221–9.CrossRefPubMed
82.
go back to reference Jungbluth H, Davis MR, Müller C, et al. Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations. Neuromuscul Disord. 2004;14(12):785–90.CrossRefPubMed Jungbluth H, Davis MR, Müller C, et al. Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations. Neuromuscul Disord. 2004;14(12):785–90.CrossRefPubMed
83.
go back to reference Klein A, Jungbluth H, Clement E, et al. Muscle magnetic resonance imaging in congenital myopathies due to ryanodine receptor type 1 gene mutations. Arch Neurol. 2011;68(9):1171–9.CrossRefPubMed Klein A, Jungbluth H, Clement E, et al. Muscle magnetic resonance imaging in congenital myopathies due to ryanodine receptor type 1 gene mutations. Arch Neurol. 2011;68(9):1171–9.CrossRefPubMed
84.
go back to reference van der Ploeg AT, Clemens PR, Corzo D, et al. A randomized study of alglucosidase alfa in late-onset Pompe’s disease. N Engl J Med. 2010;362(15):1396–406.CrossRefPubMed van der Ploeg AT, Clemens PR, Corzo D, et al. A randomized study of alglucosidase alfa in late-onset Pompe’s disease. N Engl J Med. 2010;362(15):1396–406.CrossRefPubMed
85.
go back to reference Del Gaizo A, Banerjee S, Terk M. Adult onset glycogen storage disease type II (adult onset Pompe disease): report and magnetic resonance images of two cases. Skelet Radiol. 2009;38(12):1205–8.CrossRef Del Gaizo A, Banerjee S, Terk M. Adult onset glycogen storage disease type II (adult onset Pompe disease): report and magnetic resonance images of two cases. Skelet Radiol. 2009;38(12):1205–8.CrossRef
86.
go back to reference Pichiecchio A, Uggetti C, Ravaglia S, et al. Muscle MRI in adult-onset acid maltase deficiency. Neuromuscul Disord. 2004;14(1):51–5.CrossRefPubMed Pichiecchio A, Uggetti C, Ravaglia S, et al. Muscle MRI in adult-onset acid maltase deficiency. Neuromuscul Disord. 2004;14(1):51–5.CrossRefPubMed
87.
go back to reference Carlier R-Y, Laforet P, Wary C, et al. Whole-body muscle MRI in 20 patients suffering from late onset Pompe disease: involvement patterns. Neuromuscul Disord. 2011;21(11):791–9.CrossRefPubMed Carlier R-Y, Laforet P, Wary C, et al. Whole-body muscle MRI in 20 patients suffering from late onset Pompe disease: involvement patterns. Neuromuscul Disord. 2011;21(11):791–9.CrossRefPubMed
88.
go back to reference Argov Z, Löfberg M, Arnold DL. Insights into muscle diseases gained by phosphorus magnetic resonance spectroscopy. Muscle Nerve. 2000;23(9):1316–34.CrossRefPubMed Argov Z, Löfberg M, Arnold DL. Insights into muscle diseases gained by phosphorus magnetic resonance spectroscopy. Muscle Nerve. 2000;23(9):1316–34.CrossRefPubMed
89.
go back to reference Witting N, Duno M, Piraud M, Vissing J. Severe axial myopathy in McArdle disease. JAMA Neurol. 2014;71(1):88–90.CrossRefPubMed Witting N, Duno M, Piraud M, Vissing J. Severe axial myopathy in McArdle disease. JAMA Neurol. 2014;71(1):88–90.CrossRefPubMed
90.
go back to reference Jurkatt-Rott K, Weber MA. Lehmann-horn F. MRI in muscle channelopathies. In: Weber MA, editor. Magnetic resonance imaging of the skeletal musculature. Berlin: Springer-Verlag; 2013. p. 271–88.CrossRef Jurkatt-Rott K, Weber MA. Lehmann-horn F. MRI in muscle channelopathies. In: Weber MA, editor. Magnetic resonance imaging of the skeletal musculature. Berlin: Springer-Verlag; 2013. p. 271–88.CrossRef
91.
go back to reference Amarteifio E, Nagel AM, Weber M-A, Jurkat-Rott K, Lehmann-Horn F. Hyperkalemic periodic paralysis and permanent weakness: 3-T MR imaging depicts intracellular 23Na overload—initial results. Radiology. 2012;264(1):154–63.CrossRefPubMed Amarteifio E, Nagel AM, Weber M-A, Jurkat-Rott K, Lehmann-Horn F. Hyperkalemic periodic paralysis and permanent weakness: 3-T MR imaging depicts intracellular 23Na overload—initial results. Radiology. 2012;264(1):154–63.CrossRefPubMed
92.
go back to reference Tomasová Studynková J, Charvát F, Jarosová K, Vencovsky J. The role of MRI in the assessment of polymyositis and dermatomyositis. Rheumatology (Oxford). 2007;46(7):1174–9.CrossRef Tomasová Studynková J, Charvát F, Jarosová K, Vencovsky J. The role of MRI in the assessment of polymyositis and dermatomyositis. Rheumatology (Oxford). 2007;46(7):1174–9.CrossRef
Metadata
Title
Whole-body MRI and pathological findings in adult patients with myopathies
Authors
Xavier Tomas
Jose Cesar Milisenda
Ana Isabel Garcia-Diez
Sergio Prieto-Gonzalez
Marie Faruch
Jaime Pomes
Josep Maria Grau-Junyent
Publication date
01-05-2019
Publisher
Springer Berlin Heidelberg
Published in
Skeletal Radiology / Issue 5/2019
Print ISSN: 0364-2348
Electronic ISSN: 1432-2161
DOI
https://doi.org/10.1007/s00256-018-3107-1

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