Differential diagnosis of idiopathic inflammatory myopathies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Rheumatology
Link
http://link.springer.com/content/pdf/10.1007/s11926-996-0023-5.pdf
Reference52 articles.
1. Dalakas MC: Muscle biopsy findings in inflammatory myopathies. Rheum Dis Clin North Am 2002, 28:779–798. An excellent summary of the key histopathologic features of dermatomyositis, polymyositis, and IBM. The author does not adequately address the classification of myositis patients who lack the specific histopathologic features of these three forms of IIM.
2. Zampieri S, Ghirardello A, Iaccarino L, et al.: Anti-Jo-1 antibodies. Autoimmunity 2005, 38:73–78.
3. van der Meulen MF, Bronner IM, Hoogendijk JE, et al.: Polymyositis: an overdiagnosed entity. Neurology 2003, 61:316–321. In this retrospective follow-up study of 165 patients with autoimmune myositis, polymyositis was the least common form when defined pathologically by the presence of lymphocytes surrounding and preferably invading non-necrotic muscle fibers. Most of the patients had a myositis with strictly perimysial/perivascular infiltrates or a non-inflammatory necrotizing myopathy that could not be further categorized.
4. Tsokos GC, Moutsopoulos HM, Steinberg AD: Muscle involvement in systemic lupus erythematosus. JAMA 1981, 246:766–768.
5. Ghirardello A, Zampieri S, Iaccarino L, et al.: Anti-Mi-2 antibodies. Autoimmunity 2005, 38:79–83.
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