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Predictive factors and unfavourable prognostic factors of interstitial lung disease in patients with polymyositis or dermatomyositis: a retrospective study. Patients who presented with fever tended to have a higher frequency of PM/DM-associated ILD. A Hamman-Rich-like presentation, ADM-ILD, cardiac involvement and hypoalbuminemia were poor The unfavourable prognostic factors of ILD were Gottron' s rash (chi2 = 5.35, P <0.05), cardiac impairment (chi2 = 5.68, P < 0.05) and pulmonary fibrosis (chi2 = 5.42, P <0.05) by survival analysis. CONCLUSION: The occurrence of ILD in PM/ DM patients was closely correlated to Gottron's rash, age > or = 40 years, arthralgia and fever. 2014-06-06 2018-12-01 Polymyositis is an idiopathic inflammatory myopathy characterized by symmetrical, proximal muscle weakness, elevated skeletal muscle enzyme levels, and characteristic electromyography, and muscle biopsy findings.

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in treatment of refractory polymyositis (PM) and dermatomyositis (DM). Två specifika typer av denna sjukdom är polymyositis och dermatomyositis. riskfaktorer. http://myonet.eu/myositis/genetic-and-environmental-risk-factors/. http://www.webmd.com/a-to-z-guides/myositis-symptoms-treatments-prognosis#1.

Polymyositis following Vogt-KoyanagiHarada-like syndrome in a jack Complications and prognostic factors in Vogt-Koyanagi-Harada disease.

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Independent unfavorable prognostic signs were: failure to induce remission, leukocytosis, fever, older age, a shorter disease history, and dysphagia. PMID: 3977973 findings as prognostic factors for PM/DM-ILD, such as old age [4], skin ulcer, ILD with low serum creatine kinase (CK) [5], non-Caucasian race, male sex [6], and Dermatomyositis and polymyositis subgroups had slightly different significant prognostic factors for death: old age, cancer, pulmonary interstitial fibrosis and asthenia-anorexia for dermatomyositis; old age, failure to improve muscle strength in response to treatment after one month, and the absence of myalgia as presenting symptom for polymyositis.

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Like all types of myositis, it is thought to be down to a number of factors both genetic and environmental, and nothing a particular individual has done themselves. Many doctors and researchers worldwide are looking into the cause of myositis. Polymyositis. Spierontstekingsziekte die aanleiding geeft tot spierzwakte en Men moet steeds bedacht zijn op een begeleidende kanker als voorbeschikkende factor. Univariate and multivariate analyses for potential prognostic factors of patients with DM/PM were performed by Cox proportional hazards model.

Independent unfavorable prognostic signs were: failure to induce remission, leukocytosis, fever, older age, a shorter disease history, and dysphagia. PMID: 3977973 2018-01-11 · The predictive prognostic factors for polymyositis/dermatomyositis-associated interstitial lung disease Abstract. Interstitial lung disease (ILD) is the principal cause of death in polymyositis/dermatomyositis (PM/DM).
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Conclusion: The poor prognostic factors in anti-ARS-positive patients were anti-PL-7 Ab, old age at onset , male , high dose of maintenance glucocorticoid , no use of immunosuppressant. Moreover, anti-EJ have poorest survival after more than 15 years follow-up as well as anti-PL-7. 2014-06-06 · Interstitial lung disease (ILD) is a common manifestation of polymyositis (PM), dermatomyositis (DM), and clinically amyopathic dermatomyositis (CADM); however, little is known about the factors influencing the prognosis for PM/DM/CADM-associated ILD. (PM/DM/CADM-ILD). The aim of the present study is to assess prognostic factors for PM/DM/CADM-ILD.

2021-01-05 · The factors triggering a T-cell–mediated process in polymyositis are unclear. Viruses have been implicated; so far, however, the only viruses that have been etiologically connected with the disease are the human retroviruses human immunodeficiency virus (HIV) and human T-cell lymphotrophic virus type I (HTLV-I), the simian retroviruses, and coxsackievirus B. Polymyositis is another paraneoplastic syndrome associated with lung cancer and presents clinically as a subacute myopathy that evolves over weeks to months, along with weakness of the proximal muscles.
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Polymyositis shares many symptoms with autoimmune diseases. 2021-03-03 · Other prognostic factors included ground glass opacity/attenuation (GGO/GGA) and extent of radiological abnormality. The quality of the presented evidence was rated as either low or very low. Polymyositis is an idiopathic inflammatory myopathy characterized by symmetrical, proximal muscle weakness, elevated skeletal muscle enzyme levels, and characteristic electromyography, and muscle biopsy findings. Polymyositis and dermatomyositis have many shared clinical features but have unique features on biopsy. Clinical features. Most common reported feature is muscle weakness (97%), typically proximal symmetric weakness that progresses slowly.