Although polymyositis and dermatomyositis are regarded as treatable disorders, prognosis is not well known, as in the literature long-term outcome and prognostic factors vary widely.

Other medications prescribed for polymyositis include mycophenolate mofetil (CellCept), cyclosporine and tacrolimus. Rituximab (Rituxan). More commonly used to treat rheumatoid arthritis, rituximab is an option if initial therapies don't adequately control your polymyositis symptoms.

Usually, polymyositis affects the muscles that are closest to the trunk of the body. Eventually, people with polymyositis have trouble when rising from a sitting position, climbing stairs, lifting objects, or reaching overhead. Hello! I hope this is the right place to post. A good friend of mine was diagnosed with polymyositis last month, and I am hoping someone can tell me what this means in terms of prognosis.

One hundred and seventy-six patients with PM and 72 patients with DM diagnosed in Finland in 1969–1985 were selected from the national hospital To date, only a few investigators have assessed the long‐term outcome of ILD in PM/DM patients (5, 7, 9, 10). One study of 27 DM patients found pulmonary involvement to be the most frequent cause of death over a 10‐year followup period . In the present study, 7.5% of our patients died, mainly of ILD complications (87.5% of cases). Polymyositis is a rare autoimmune, at times considered paraneoplastic, inflammatory condition characterized by proximal muscle weakness . It is considered a form of idiopathic inflammatory myopathy (IIM).

doi: 10.3109/14397595.2015.1054081. Epub 2015 Jun 13. Long-term follow-up of 124 patients with polymyositis and dermatomyositis: Statistical analysis of prognostic factors.

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Arthritis Rheum. 1971;14:249-258. http://www.ncbi.nlm.nih.gov/pubmed/5549971?tool=bestpractice.com [106] Maugar YM, Berthelot JM, Abbas AA, et al.

Time between salivary gland biopsy and NHL diagnosis was in median 8 yrs Long-chain polyunsaturated fatty acid composition in plasma, adipose tissue and Objectives: To investigate whether Caucasian patients with polymyositis (PM)

It is considered a form of idiopathic inflammatory myopathy (IIM).

The hands, feet, and face are not usually affected. Although there is no cure for polymyositis, treatment can improve muscle strength and function. With treatment, prognosis has improved with 5-year survival of 95% and 10-year survival of 84%. Marie I, Hachulla E, Hatron PY, et al. Polymyositis and dermatomyositis: short term and longterm outcome, and predictive factors of prognosis. Polymyositis is a chronic illness featuring progressive muscle weakness with periods of increased symptoms, called flares or relapses, and minimal or no symptoms, known as remissions.
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Abstract. Objective. To assess the long-term outcome in polymyositis (PM) The prognosis for polymyositis varies.

Marie I, Hachulla E, Hatron PY, et al.
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ASS was associated with decreased quality of life at long-term follow-up: only 69.2% of patients considered to be in remission experienced a return to previous normal activities; and 24.7% of

It affects all age groups, although its onset is most common in middle childhood and in the 20s. The prognosis of dermatomyositis and polymyositis was poor before the availability of corticosteroids.