Dermatomyositis. Diagnostic and therapeutic recommendations of the Polish Dermatological Society

Dermatomyositis is an autoimmune disease characterized by skin lesions and/or symptoms of myositis. In addition to the so-called classic dermatomyositis the following forms of dermatomyositis are distinguished based on the clinical presentation: pediatric, paraneoplastic, drug-induced and amyopathic...

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Main Authors: Adam Reich (Author), Anna Lis-Święty (Author), Dorota Krasowska (Author), Joanna Maj (Author), Joanna Narbutt (Author), Anna Sysa-Jedrzejowska (Author), Anna Wojas-Pelc (Author), Anna Woźniacka (Author), Lidia Rudnicka (Author)
Format: Book
Published: Termedia Publishing House, 2021-06-01T00:00:00Z.
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100 1 0 |a Adam Reich  |e author 
700 1 0 |a Anna Lis-Święty  |e author 
700 1 0 |a Dorota Krasowska  |e author 
700 1 0 |a Joanna Maj  |e author 
700 1 0 |a Joanna Narbutt  |e author 
700 1 0 |a Anna Sysa-Jedrzejowska  |e author 
700 1 0 |a Anna Wojas-Pelc  |e author 
700 1 0 |a Anna Woźniacka  |e author 
700 1 0 |a Lidia Rudnicka  |e author 
245 0 0 |a Dermatomyositis. Diagnostic and therapeutic recommendations of the Polish Dermatological Society 
260 |b Termedia Publishing House,   |c 2021-06-01T00:00:00Z. 
500 |a 0033-2526 
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500 |a 10.5114/dr.2021.107278 
520 |a Dermatomyositis is an autoimmune disease characterized by skin lesions and/or symptoms of myositis. In addition to the so-called classic dermatomyositis the following forms of dermatomyositis are distinguished based on the clinical presentation: pediatric, paraneoplastic, drug-induced and amyopathic. A number of disease-specific autoantibodies are identified in dermatomyositis (including anti-Mi2, anti-TIF1, anti-NXP2, anti-SAE or anti-MDA5), presence of which may be associated with a specific clinical phenotype. The diagnosis of the severity of muscle involvement is currently based mainly on physical examination, deviations in results of laboratory investigations, electromyographic examination and imaging examination, mainly with the use of magnetic resonance imaging. Systemic glucocorticosteroids administered as monotherapy or in combination with other immunosuppressants remain the mainstay of dermatomyositis treatment, and in the absence of satisfactory improvement, intravenous immunoglobulins are used. In addition, in case of interstitial lung disease, the use of cyclophosphamide may be necessary. The choice of a therapy, as well as the rate of dose reduction, depend on the dynamics of the disease, symptoms, diagnosed immunological disorders, as well as comorbidities and the drugs used. Each diagnostic and therapeutic decision must take into account the individual clinical data of the patient and current scientific reports. 
546 |a EN 
546 |a PL 
690 |a dermatomyositis 
690 |a  idiopathic inflammatory myopathies 
690 |a  autoimmune diseases of connective tissue 
690 |a  treatment. 
690 |a Medicine 
690 |a R 
690 |a Dermatology 
690 |a RL1-803 
655 7 |a article  |2 local 
786 0 |n Przegląd Dermatologiczny, Vol 108, Iss 2, Pp 85-104 (2021) 
787 0 |n https://www.termedia.pl/Dermatomyositis-Diagnostic-and-therapeutic-recommendations-r-nof-the-Polish-Dermatological-Society,56,44511,1,1.html 
787 0 |n https://doaj.org/toc/0033-2526 
787 0 |n https://doaj.org/toc/2084-9893 
856 4 1 |u https://doaj.org/article/cacbaa1c3f1b47a19a69d4c35b337ffd  |z Connect to this object online.