This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Polymyositis and dermatomyositis

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Polymyositis and dermatomyositis are systemic connective tissue diseases which are characterised by acute and chronic inflammation of striated muscle. In dermatomyositis there is an accompanying dermatitis. The limb girdle or proximal muscles are most severely affected but their bulk is preserved beyond that expected from their weakness: this is an important sign distinguishing this condition from a limb girdle dystrophy.

Myositis is usually the initial presentation. Some patients present with dermatitis and later develop muscle weakness; rarely, only dermatitis occurs.

The aetiology is unknown but there is an association with HLA-B8 and HLA-DR3.

Dermatomyositis in males over the age of 60 years may be suggestive of an underlying systemic malignancy.

Clinical features of dermatomyositis include:

  • possible dermatological features include
    • a heliotrope rash (a red-to-violet - colored rash around the eyes that might be accompanied by swelling)
    • Gottron papules (red bumps most prominently seen on the knuckles of the hands)
    • other characteristic dermatological findings include:
      • red purplish discoloration on the face, exposed surfaces of the arms, forearms and hands, scalp, upper chest, upper back (known as a Shawl sign), and the lateral hips (known as the holster sign) in addition to changes around the cuticles of the fingernails
      • photosensitivity may occur (1)
  • myopathic symptoms
    • muscle inflammation tends to affect larger muscles and can present as difficulty raising the arms above the shoulder or trouble rising from a chair or climbing stairs (1)
    • occasionally there is muscle tenderness, fatigue, and low-grade fever
  • dermatomyositis can also affect the oesophagus, lungs, or heart

Treatment options include:

  • glucocorticoids with or without second-line immunosuppressive agents including methotrexate, azathioprine, mycophenolate mofetil, and, in refractory cases, IVIG (intravenous immunoglobulin) or rituximab
  • in a 16-week trial involving adults with dermatomyositis, the percentage of patients with a response of at least minimal improvement based on a composite score of disease activity was significantly greater among those who received IVIG than among those who received placebo (2)

Click here for example images of this condition

Reference:

  • Callen JP. Dermatomyositis. JAMA Dermatol. Published online July 05, 2023. doi:10.1001/jamadermatol.2023.1013
  • Aggarwal R et al. Trial of Intravenous Immune Globulin in Dermatomyositis N Engl J Med 2022; 387:1264-1278.

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.