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Polymyositis/Dermatomyositis

Christopher M. Wise, MD and Nehal R. Shah, MD Reviewed 05/2023
 


BASICS

DESCRIPTION

  • Systemic connective tissue disease characterized by inflammatory and degenerative changes in proximal muscles, sometimes accompanied by characteristic skin rash

    • If skin manifestations...

DIAGNOSIS

HISTORY

  • Symmetric proximal muscle weakness causing difficulty when

    • Arising from sitting or lying positions

    • Climbing stairs

    • Raising arms

  • Joint pain/swelling

  • Dysphagia

  • Dyspnea

  • Rash on face, eyelids, h...

TREATMENT

GENERAL MEASURES

T Approach to treatment has varied by specialty involved (dermatology, rheumatology, neurology). Treatment approach should be informed by lesion type, degree of muscle involv...

ONGOING CARE

FOLLOW-UP RECOMMENDATIONS

Patient Monitoring

  • Follow muscle enzymes along with muscle strength and functional capacity.

  • Monitor for steroid-induced complications (e.g., hypokalemia, hypertens...

REFERENCES

1
Senécal  JL, Raynauld  JP, Troyanov  Y. Editorial: a new classification of adult autoimmune myositis. Arthritis Rheumatol.  2017;69(5):878–884. [View Abstract ...

ADDITIONAL READING

 Mammen AL. Statin-associated autoimmune myopathy.  N Engl J Med. 2016;374(7):664–669  

CODES

ICD10

  • M33.20 Polymyositis, organ involvement unspecified

  • M33.90 Dermatopolymyositis, unspecified, organ involvement unspecified

  • M33.92 Dermatopolymyositis, unspecified with myopathy

  • M33.22 Polymyosi...

CLINICAL PEARLS

  • Corticosteroids alone may be sufficient in patients who have rapid improvement in weakness and muscle enzymes. However, most patients require azathioprine, methotrexate, or other immun...

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