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Psoriatic plaque, showing a silvery center surrounded by a reddened border. Psoriasis vulgaris (also known as chronic stationary psoriasis or plaque-like psoriasis) is the most common form and affects 85–90% of people with psoriasis. [13] Plaque psoriasis typically appears as raised areas of inflamed skin covered with silvery-white, scaly ...
Three stages characterize the evolution of necrolytic acral erythema lesions: early, well-developed, and late. Scaly, erythematous papules or plaques with a distinctively dark or worn center first emerge. When the lesions reach a well-developed stage, they combine to create a thick, hyperpigmented plaque that is clearly defined and has adhering ...
Psoriasis. What it looks like: Psoriasis causes patches of thickened skin, most often with silver, scaly flakes.It’s usually found around the elbows, feet, knees, palms, and you can even have ...
Psoriasis is a common, chronic, and recurrent inflammatory disease of the skin characterized by circumscribed, erythematous, dry, scaling plaques. [ 97 ] [ 98 ] [ 99 ] Psoriasis vulgaris
The plaque stage follows the patch stage of mycosis fungoides. [3] It is characterized by the presence of raised lesions that appear reddish-brown; in darker skin tones, plaques may have a greyish or silver appearance. [4] Both patch and plaque stages are considered early-stage mycosis fungoides. [3]
Parakeratosis is seen in the plaques of psoriasis and in dandruff. 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. It presents in all age groups and has no ...
Alopecia mucinosa, also known as Follicular mucinosis, Mucinosis follicularis, Pinkus' follicular mucinosis, and Pinkus' follicular mucinosis–benign primary form, is a skin disorder that generally presents, but not exclusively, as erythematous plaques or flat patches without hair primarily on the scalp, neck and face.
PLC presents with a far slower clinical course than both febrile ulceronecrotic Mucha-Habermann disease and PLEVA. Similar to PLC, the lesion begins as an erythematous papule that turns reddish-brown and is easily detached to reveal a shiny, pinkish-brown surface. The lesion also has a centrally adherent micaceous scale.