parakeratosis

In mucous membranes, parakeratosis is normal.

Histological scoring took into account hypogranulosis, parakeratosis and the inflammatory infiltrate in the epidermis and superficial dermis.

Actinic keratosis usually shows focal parakeratosis with associated loss of the granular layer of, and thickening of the epidermis.

Occasionally non-specific staining was noted with AEC at the surperficial layers of normal epithelium demonstrating parakeratosis.

Other conditions noted have been cement dermatitis, collagen deposits, discoid lupus erythematosus, eczematous eruptions, hyperkeratosis and parakeratosis, and keloids.

Inflammatory linear verrucous epidermal nevi are skin lesions that follow the lines of Blaschko, characterized histologically by hypergranulosis with orthokeratosis and parakeratosis with agranulosis.

Parakeratosis pustulosa is a cutaneous condition which is exclusively seen in children, usually involving one finger, most commonly the thumb or index finger, with the affected nail showing subungual hyperkeratosis and onycholysis.

Tissue biopsy is not indicated, but when taken, the histologic appearance is one of increased epithelial thickness, broadening and eleongation of the rete ridges, parakeratosis and intracellular edema of the spinous layer.

Genital warts, histopathologically, characteristically rise above the skin surface due to enlargement of the dermal papillae, have parakeratosis and the characteristic nuclear changes typical of HPV infections (nuclear enlargement with perinuclear clearing).

A study by Warner et al. demonstrates a dramatic reduction of structural abnormalities found in dandruff with the use of ZPT; the population abundance of Malassezia decreases, parakeratosis gets eliminated and corneocytes lipid inclusions are diminished.

Granular parakeratosis (originally termed axillary granular parakeratosis) is an idiopathic, benign, nondisabling cutaneous disease that manifests with intertriginous erythematous, brown or red, scaly or keratotic papules and plaques.

Granular parakeratosis (also known as "Axillary granular parakeratosis," and "Intertriginous granular parakeratosis") is a cutaneous condition characterized by brownish-red keratotic papules that can coalesce into plaques.