M33.13
BillableOther dermatomyositis without myopathy
HCC Category Mapping
V28HCC 93 — Rheumatoid Arthritis and Inflammatory Connective Tissue Disease
0.175V24HCC 40 — Rheumatoid Arthritis and Inflammatory Connective Tissue Disease
0.307ESRDHCC 40 — Rheumatoid Arthritis and Inflammatory Connective Tissue Disease
0.000RxHCCHCC 83 — Rheumatoid Arthritis and Inflammatory Connective Tissue Disease
0.000What This Code Means
A rare autoimmune disease causing a characteristic skin rash and inflammation without significant muscle weakness or damage.
Coding Tips
- •Confirm documentation explicitly states absence of myopathy or muscle involvement
- •Ensure skin manifestations are documented (heliotrope rash, Gottron papules) to support dermatomyositis diagnosis
Clinical Significance
Adult dermatomyositis without myopathy, often called amyopathic dermatomyositis, still carries significant risks including interstitial lung disease and malignancy. This form requires the same vigilant monitoring and treatment as classic dermatomyositis despite preserved muscle strength.
Documentation Requirements
- ✓Confirmed adult dermatomyositis diagnosis
- ✓Characteristic skin manifestations documented
- ✓Documentation of absent or minimal muscle weakness
- ✓Normal or minimally elevated muscle enzymes
- ✓Preserved muscle strength on examination
- ✓Malignancy screening completed
- ✓Lung function assessment performed
- ✓Treatment plan for skin and systemic involvement