Granular Parakeratosis
Last Updated: 2026-02-09
Author(s): Navarini A.A.
ICD11: -
Last Updated: 2026-02-09
Author(s): Navarini A.A.
ICD11: -
Granular parakeratosis; Intertriginous parakeratotic hyperkeratosis; Axillary granular parakeratosis.
Granular parakeratosis is a rare, benign, inflammatory keratinization disorder that primarily affects intertriginous areas. Histologically characterized by retention of keratohyalin granules within parakeratotic stratum corneum cells, it reflects a defect in the normal conversion of profilaggrin to filaggrin.
Rare. Most common in middle-aged women, but also reported in infants (infantile form). Often associated with topical irritants, occlusion, or friction (e.g., deodorants, zinc oxide, moisturizers, barrier creams).
Belongs to the group of acquired disorders of keratinization. Clinically and histopathologically distinct from psoriasis, eczema, and acantholytic dermatoses.
The exact cause remains unclear. Likely due to a defect in stratum corneum maturation, with impaired degradation of profilaggrin to filaggrin and persistence of keratohyalin granules. Contributing factors include:
Preferentially affects intertriginous regions: axillae, groin, inframammary folds, perianal area. In infants, mostly confined to diaper region.
Gradually evolving plaques in areas of friction or occlusion. Often linked to use of topical products. No systemic symptoms.
Benign. Often self-limited after removal of the triggering factor. Chronic or recurrent in cases with ongoing exposure to irritants or occlusion.
Avoidance of occlusive, irritant, or fragranced products in intertriginous areas. Use of breathable clothing and barrier-reducing hygiene.
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