Publication details

Dermatomyozititida asociovaná s cytomegalovirovou infekcí

Title in English Dermatomyositis associated with cytomegalovirus infection
Authors

NOVÁKOVÁ Michaela JEDLIČKOVÁ Hana TVRDÍKOVÁ Eliška VAŠKŮ Vladimír

Year of publication 2017
Type Article in Periodical
Magazine / Source Česká dermatovenerologie
MU Faculty or unit

Faculty of Medicine

Citation
Field Dermatovenerology
Keywords inflammatory myopathies; dermatomyositis; cytomegalovirus; methylprednisolon; methotrexate
Description Inflammatory myopathies are acquired autoimmune diseases, clinically characterized by weakness and soreness of muscles and elevated muscle enzymes - creatine kinase and lactate dehydrogenase, his-topathologically by myonecrosis and mo- nonuclear inflammatory infiltrate. The most common inflammatory myopathies are dermatomyositis, polymyositis, and inclusion body myositis. Dermatomyositis is a rare inflammatory disease with autoimmune features marked by muscle weakness and a distinctive skin rash - a heliotrope rash on the face, fleeting erythema on the extensor surfaces, erythematous papules over the small knuckles (Gottron's sign) etc. Other frequent symptoms are muscle contractu-res, subcutaneous calcification, intestinal ulceration. Dermatomyositis affects adults and children alike. In children, the disease most often appears between 5 and 15 years of age. In adults, dermatomyositis usually occurs from the late 30s to early 60s. Dermatomyositis affects more females than males. The case of dermatomyositis in a 37-year old woman with acute cytomegalovirus infection, succesfully treated with combination od methylprednisolon and me-thotrexate, is described in the presented case study.

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