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A Case of Acral Persistent Papular Mucinosis
2003
Annals of Dermatology
Acral persistent papular mucinosis has been thought to be a distinct form of cutaneous mucinosis not associated with systemic diseases. It was recently classified as one of five subtypes of localized lichen mixedematosus. A 64-year-old man presented with a 15-year history of fleshcolored to translucent papules and a few round hypopigmented patches on his wrists, back of the hands, and distal forearms. Biopsy from the papular lesions revealed focal mucin accumulation in the upper reticular
doi:10.5021/ad.2003.15.1.8
fatcat:3flamtorxjgnvmrvy5mzyxgmla