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Marie I, Hachulla E, Hatron PY, et al. Polymyositis and dermatomyositis: short term and longterm outcome, and predictive factors of prognosis. Heterogeneous group of muscular disorders characterised by progressive muscle weakness. Presentation is sub-acute or chronic and rarely acute. May be associated with dysphagia, fatigue, difficulties with breathing, and skin lesions. Diagnosis is confirmed by … Polymyositis is a connective tissue disease that triggers inflammation and muscular weakness.

Osteoporosis, a common complication of long-term corticosteroid therapy, may cause significant morbidity. Poor prognostic factors are. Advanced age; Female sex; Interstitial lung disease 2021-01-04 Polymyositis prognosis The prognosis for polymyositis varies. Most people respond fairly well to therapy, but some have a more severe disease that does not respond adequately to therapies and are left with significant disability. In rare cases individuals with severe and progressive muscle weakness will develop respiratory failure or pneumonia. 2020-07-02 Polymyositis (PM) is an idiopathic inflammatory myopathy (IIM) long-term prognosis, and activity limitations. Data is limited on the efficacy and long-term toxicity of immunosuppressants in IIM in the pediatric population.

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9 Polymyositis prognosis The prognosis for polymyositis varies. Most people respond fairly well to therapy, but some have a more severe disease that does not respond adequately to therapies and are left with significant disability.

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Long-term follow-up of 124 patients with polymyositis and dermatomyositis: Statistical analysis of prognostic factors. 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. 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. Polymyositis causes muscles to become irritated and inflamed.

Several years of treatment to suppress the immune system may be necessary to achieve these results. Polymyositis and Dermatomyositis: Short Term and Longterm Outcome, and Predictive Factors of Prognosis ISABELLE MARIE, ERIC HACHULLA, PIERRE-YVES HATRON, MARIE-FRANCE HELLOT, HERVE LEVESQUE, BERNARD DEVULDER, and HUBERT COURTOIS ABSTRACT. Objective. To assess short term and longterm outcome of polymyositis (PM) and dermatomyositis Hi,I have had Polymyositis for 3.5 years now .I am 74..I lost a lot of weight in first 5 months & a lot of muscle wasting ,as well as swallowing problems.I have fairly well gotten over the swallowing problem & by building a big extension onto our house ,building frames,putting up gyprock,tiling ,painting ,etc & using my upper body to help me It is also related to mortality. Previous studies have highlighted that the acute form of PM/DM/CADM-associated ILD (PM/DM/CADM-ILD) has a poor short-term prognosis. However, little is known about the long-term clinical features of patients with PM/DM/CADM-ILD. Background: 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.
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Se hela listan på mayoclinic.org Polymyositis, which affects many different muscles, particularly the shoulders, hips and thigh muscles. It's more common in women and tends to affect people aged 30 to 60. Dermatomyositis, which affects several muscles and causes a rash. It's more common in women and can also affect children (juvenile dermatomyositis).

The condition can affect swallowing and breathing. Although it can't be cured, the symptoms of polymyositis can be managed. Next steps. Tips to help you get the most from a visit to your healthcare provider: Maugars YM, Berthelot JM, Abbas AA, Mussini JM, Nguyen JM, Prost AM: Long-term prognosis of 69 patients with dermatomyositis or polymyositis.
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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).