Introduction: Dermatomyositis (DM) is an inflammatory disease classified among
autoimmune diseases affecting young and older individuals. Due to its nonspecific
symptoms and insidious onset, patients and primary care physicians
often overlook it. Delayed diagnosis postpones the initiation of effective
treatment and causes irreversible damage to the body. Aim of the study: This study
reviews the current literature on the clinical presentation, diagnosis, and
treatment of dermatomyositis. It also summarises existing knowledge in this
field. Summary of knowledge: Diagnosis of DM relies on clinical symptoms,
including muscle weakness and skin lesions. Decreased strength in the shoulder
and hip muscles hinders basic tasks like combing hair or climbing stairs. Late
diagnosis can lead to severe musculoskeletal issues. Optimizing treatment
outcomes involves tailoring the regimen to the lesion type, muscle involvement,
specific autoantibodies, and the patient’s age. Conclusion: Early diagnosis and
timely initiation of treatment are crucial for managing dermatomyositis and
enhancing the quality of life for patients. Despite the availability of various
treatments, achieving clinical remission remains challenging for many patients.
This highlights the need for continued research to develop more effective
therapies and strategies for managing this complex disease.
Keywords: Dermatomyositis; Idiopathic Inflammatory Myopathy; Motor activity
impact; Symmetrical muscle weakness
