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Dermatomyositis (DM)/Polymyositis (PM)

Polymyostitis is severe inflammation of proximal striated muscle. DM – when skin is also affected

Etiology

  • Virus – coxsachie, rubella, influenza
  • HLA DR3 (others = Myasthenia gravis, Hashimoto, T1DM, primary sclerosing cholangitis)
  • Can be associated w/ sjogrens, SSc, SLE

CF

  • Adult PM
    • Female, insidious, malaise, fever, WL, proximal muscle weakness (shoulder)
    • Face and distal limbs spared. Larynx/pharynx/respire muscles in advanced disease
  • Adult DM
      • Characteristic rash – eyes have purple discolouration and periorbital edema. Gottrons papules – vasculitis patches over knuckles
    • Myalgia, polyarthritis, raynauds
    • Ulcerative vasculitis and calcinosis of subcutaneous tissue
  • Antisynthase syndrome
    • tRNA synthase antibody = poor prognosis, pts develop pulmonary interstitial fibrosis and hand contractures. Dysphagia is also common.
  • Childhood DM
    • 4-10y, features same as above

Diagnosis

  • Creatinine kinase, LDH, aldolase – muscle damage
  • Antibodies – tRNA-ab, ANA, RF
  • EMG – triad for myositis = 1. spontaneous fibrillations at rest, 2.short PO on contraction, 3. repetitive PO on mechanical nerve stimulation
  • PET/malignancy screening

DDx

  • All haematological conditions. Auto antibodies and EMG strong evidence for diagnosis.

Treatment

  • Prednisolone [0.5-1 mg/kg] until no myositis
  • If advanced features use methylprednisolone 1g/day for 3 days
  • Steroid sparring – methotrexate [25mg/week], azathioprine, cyclosporin, mycophenolate
  • IVIG
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