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Wheeless' Textbook of Orthopaedics
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Dermatomyositis and Polymyositis



- See:
      - Myopathic Disorders
      - Ossification of Soft Tissue and Periosteum:

- Discussion:
    - most common collagen vascular diseases which affect muscle;
    - pts may be affected at any age;
    - may be due to viral infection;
    - in adults, note possible concomitant occult neoplasm;

- Clinical Findings:
    - systemic illness;
    - muscle and joint tenderness;
    - progressive weakness which begins in proximal girdle;
    - dermatomyositis:
          - look for skin involvement w/ heliotrope rash around eyelids &
                  erythematous changes, especially over nail beds & knuckles;
          - in contrast to systemic lupus, in which phalanges are involved
                  & knuckles are spared, dermatomyositis will spare phalanges;

- Labs: CPK & Sed rate are frequently elevated;
   
- EMG:
    - EMG of myopathic disorders:
    - useful for excluding neurogenic disorders;
    - reveals short-duration, low-amplitude polyphasic units on voluntary activation;
    - increased spontaneous activity with fibrillations & positive sharp waves;
    - polyphasic units of short & long duration may be present w/ chronic disease;

- Radiographs:
    - types of dystrophic calcification: (see ossification of soft tissue)
          - superficial masses (small circumscribed nodules) within skin;
          - deep discrete subcutaneous nodular masses near joints that can impair movement (calcinosis circumscripta);
          - deep linear sheetlike deposits within intramuscular fascial planes (calcinosis universalis);

- Treatment:
    - steroid & immunosuppressive medications are useful;




Review Article: Medical Progress: Polymyositis, Dermatomyositis, And Inclusion-Body Myositis.

Patterns of calcification in childhood dermatomyositis.
      CE Blane et al.   AJR. Vol 142. 1984.   p 397-400.
















Original Text by Clifford R. Wheeless, III, MD.