M33.19
ICD-10-CMThis code signifies a systemic autoimmune inflammatory myopathy characterized by muscle weakness and a distinctive skin rash, where the patient also exhibits involvement of other organ systems beyond the skin and muscles. This "other" category implies that the specific type of dermatomyositis is not otherwise specified or falls outside of juvenile or amyopathic forms, and the organ involvement is not limited to the integumentary or musculoskeletal systems.
Apply this code when documentation confirms a diagnosis of dermatomyositis, not specified as juvenile or amyopathic, and there is clear evidence of systemic involvement affecting organs such as the lungs (e.g., interstitial lung disease), heart (e.g., myocarditis), or gastrointestinal tract. The physician's notes should explicitly state "other dermatomyositis" or a similar non-specific type, along with mention of extra-muscular, extra-cutaneous manifestations.
AI-generated reference — verify against official guidelines
+5 more in this category