LCDActive
MolDX: Pigmented Lesion Assay
L38151
Effective: June 20, 2024
Updated: December 31, 2025
Policy Summary
The Pigmented Lesion Assay (PLA) is covered as a pre-biopsy decision tool for primary melanocytic skin lesions (5–19 mm) with one or more ABCDE features when a clinician trained in skin cancer evaluation is considering biopsy. Coverage is limited to intact, non-scarred, non-ulcerated lesions not located in palms/soles/nails/mucous membranes or areas of psoriasis/eczema, requires documentation (lesion photograph, site, clinician credentials, and monitoring plan), and generally allows one test per lesion and typically one test per clinical encounter (rare exceptions require appeal).
Coverage Criteria Preview
Key requirements from the full policy
"PLA is indicated for evaluation of primary melanocytic skin lesions when a clinician trained in diagnosing skin cancer is considering whether to perform a biopsy to rule out melanoma."
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