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Autoimmune and Connective Tissue Disease

Recognize and manage systemic lupus, scleroderma, vasculitis, and inflammatory myopathies with a structured, evidence-based approach.

What this track covers

This track covers the recognition, workup, and management of major connective tissue diseases, including systemic lupus erythematosus, scleroderma, vasculitis syndromes, and inflammatory myopathies. It emphasizes classification criteria, autoantibody interpretation, and multi-system disease patterns that shape diagnosis and treatment decisions.

What you will practice

  • Distinguish limited versus diffuse scleroderma and their organ involvement patterns
  • Apply classification criteria to differentiate SLE from other connective tissue diseases
  • Interpret ANA patterns and disease-specific autoantibodies in clinical context
  • Classify vasculitis syndromes by vessel size and presentation
  • Differentiate dermatomyositis, polymyositis, and immune-mediated necrotizing myopathy

Simulator scenario

A patient presents with new proximal muscle weakness, a rash, and elevated muscle enzymes, requiring the clinician to work through the differential of inflammatory myopathies and select appropriate confirmatory testing.

Board question topics

  • SLE classification criteria and disease activity assessment
  • Scleroderma subtypes and organ involvement screening
  • Vasculitis classification by vessel size
  • Autoantibody patterns in connective tissue disease

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