Granular parakeratosis in All Ages
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Synopsis
A rare, benign, acquired disorder of keratinization due to a defect in filaggrin processing, which results in the retention of keratohyalin granules in the epidermis. GP typically presents as reddish-brown, violaceous, or hyperpigmented scaly papules and plaques in intertriginous regions. Lesions can be asymptomatic or pruritic and friable. It is most commonly caused by heat, moisture, and friction. GP has a relatively chronic course and can persist for several months or can resolve spontaneously, but recurrence is common.
Codes
ICD10CM:
L85.8 – Other specified epidermal thickening
SNOMEDCT:
56585003 – Parakeratosis of skin
L85.8 – Other specified epidermal thickening
SNOMEDCT:
56585003 – Parakeratosis of skin
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Last Updated:03/03/2022
Granular parakeratosis in All Ages
