Muscle biopsy features of idiopathic inflammatory myopathies and differential diagnosis

Springer Science and Business Media LLC - Tập 5 Số 3 - Trang 77-85 - 2014
Gaetano Vattemi1, Massimiliano Mirabella2, Valeria Guglielmi1, Matteo Lucchini2, Giuliano Tomelleri1, Anna Ghirardello3, Andrea Doria3
1Department of Neurological and Movement Sciences, Section of Clinical Neurology, University of Verona, Verona, Italy
2Istituto di Neurologia-Policlinico “A. Gemelli”, Università Cattolica, Rome, Italy
3Division of Rheumatology, Department of Medicine, University of Padua, Via Giustiniani, 35128 PADOVA, Padua, Italy

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Dimachkie MM (2011) Idiopathic inflammatory myopathies. J Neuroimmunol 231:32–42

Luo YB, Mastaglia FL (2014) Dermatomyositis, polymyositis and immune-mediated necrotising myopathies. Biochim Biophys Acta

Hoogendijk JE, Amato AA, Lecky BR, Choy EH, Lundberg IE, Rose MR et al (2004) 119th ENMC international workshop: trial design in adult idiopathic inflammatory myopathies, with the exception of inclusion body myositis. Neuromuscul Disord 14:337–345

Engel AG, Hohlfeld R, Banker BQ (2006) The polymyositis and dermatomyositis syndrome. In: Engel AG, Franzini-Armstrong C (eds) Myology. McGraw-Hill, New York, pp 1335–1383

Dalakas MC (2011) An update on inflammatory and autoimmune myopathies. Neuropathol Appl Neurobiol 37:226–242

Emslie-Smith AM, Engel AG (1990) Microvascular changes in early and advanced dermatomyositis: a quantitative study. Ann Neurol 27:343–356

De Visser M, Emslie-Smith AM, Engel AG (1989) Early ultrastructural alterations in adult dermatomyositis. Capillary abnormalities precede other structural changes in muscle. J Neurol Sci 94:181–192

Liang C, Needham M (2011) Necrotizing autoimmune myopathy. Curr Opin Rheumatol 23:612–619

Askanas V, Engel WK (2008) Inclusion-body myositis: muscle-fiber molecular pathology and possible pathogenic significance of its similarity to Alzheimer’s and Parkinson’s disease brains. Acta Neuropathol 116:583–595

Askanas V, Engel WK, Nogalska A (2012) Pathogenic considerations in sporadic inclusion-body myositis, a degenerative muscle disease associated with aging and abnormalities of myoproteostasis. J Neuropathol Exp Neurol 71:680–693

Nirmalananthan N, Holton JL, Hanna MG (2004) Is it really myositis? A consideration of the differential diagnosis. Curr Opin Rheumatol 16:684–691

Mohassel P, Mammen AL (2013) Statin-associated autoimmune myopathy and anti-HMGCR autoantibodies. Muscle Nerve 48:477–483

Stenzel W, Goebel HH, Aronica E (2012) Review: immune-mediated necrotizing myopathies–a heterogeneous group of diseases with specific myopathological features. Neuropathol Appl Neurobiol 38(7):632–646

Pestronk A, Kos K, Lopate G, Al-Lozi MT (2006) Brachio-cervical inflammatory myopathies: clinical, immune, and myopathologic features. Arthritis Rheum 54:1687–1696

Selva-O’Callaghan A, Trallero-Araguás E, Grau JM (2014) Eosinophilic myositis: An updated review. Autoimmun Rev 13:375–378

Prieto-González S, Grau JM (2014) Diagnosis and classification of granulomatous myositis. Autoimmun Rev 13:372–374

Chahin N, Selcen D, Engel AG (2005) Sporadic late onset nemaline myopathy. Neurology 65:1158–1164

Madariaga MG (2002) Polymyositis-like syndrome in hypothyroidism: review of cases reported over the past twenty-five years. Thyroid 12:331–336

Yoon J, Kim SH, Ki CS et al (2011) Carrier woman of duchenne muscular dystrophy mimicking inflammatory myositis. J Korean Med Sci 26:587–591

Schüller A, Wenninger S, Strigl-Pill N, Schoser B (2012) Toward deconstructing the phenotype of late-onset pompe disease. Am J Med Genet C Semin Med Genet 160C(1):80–88