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Clinical heterogeneity and treatment response in inclusion body myositis
Inclusion body myositis has been described as an inflammatory myopathy with distinctive clinical and pathologic features that is refractory to treatment. Ten cases of inclusion body myositis, as defined by histopathologic findings, were reviewed to determine whether the clinical characteristics are...
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Published in: | Arthritis and rheumatism 1989-06, Vol.32 (6), p.734-740 |
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container_title | Arthritis and rheumatism |
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creator | Cohen, Miriam Richter Sulaiman, A. R. Garancis, John C. Wortmann, Robert L. |
description | Inclusion body myositis has been described as an inflammatory myopathy with distinctive clinical and pathologic features that is refractory to treatment. Ten cases of inclusion body myositis, as defined by histopathologic findings, were reviewed to determine whether the clinical characteristics are different in patients whose disease has been defined by light and electron microscopic studies compared with those whose disease has been defined by light microscopic studies alone. The clinical characteristics of both groups of patients were similar, and 2 patients have had excellent responses to treatment. Although inclusion body myositis represents a histologic subset of polymyositis, from a clinical perspective, it must be considered a nonspecific designation. Despite a generally poor prognosis, therapeutic intervention is still warranted. |
doi_str_mv | 10.1002/anr.1780320611 |
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Although inclusion body myositis represents a histologic subset of polymyositis, from a clinical perspective, it must be considered a nonspecific designation. 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R.</creatorcontrib><creatorcontrib>Garancis, John C.</creatorcontrib><creatorcontrib>Wortmann, Robert L.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Arthritis and rheumatism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cohen, Miriam Richter</au><au>Sulaiman, A. 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The clinical characteristics of both groups of patients were similar, and 2 patients have had excellent responses to treatment. Although inclusion body myositis represents a histologic subset of polymyositis, from a clinical perspective, it must be considered a nonspecific designation. Despite a generally poor prognosis, therapeutic intervention is still warranted.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>2544185</pmid><doi>10.1002/anr.1780320611</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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ispartof | Arthritis and rheumatism, 1989-06, Vol.32 (6), p.734-740 |
issn | 0004-3591 1529-0131 |
language | eng |
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source | Wiley-Blackwell Journals (Backfile Content) |
subjects | Adult Aged Azathioprine - therapeutic use Biological and medical sciences Female Humans Inclusion Bodies - pathology Inclusion Bodies - ultrastructure Male Medical sciences Microscopy, Electron Middle Aged Myositis - drug therapy Myositis - pathology Neurology Prednisone - therapeutic use Time Factors |
title | Clinical heterogeneity and treatment response in inclusion body myositis |
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