M33.92
ICD-10-CMThis code signifies a form of inflammatory myopathy characterized by both muscle weakness (myositis) and skin manifestations (dermatitis), where the specific type of dermatopolymyositis is not further specified in the medical record. The presence of myopathy is explicitly documented, indicating muscle involvement.
Use this code when the physician documents "dermatopolymyositis with myopathy" without specifying a more precise subtype (e.g., juvenile, adult-onset, paraneoplastic). This code is appropriate when the clinical picture clearly indicates both skin and muscle involvement consistent with dermatopolymyositis, but further diagnostic clarity is lacking.
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