Results 21 to 30 of about 457 (152)
Disseminated superficial "actinic" porokeratosis
Acta Dermato-Venereologica, 1980 No abstract ...
D E, Hazelrigg, W F, Farrell
openaire +4 more sources
Extensive Spiculated Follicular Porokeratosis With Alopecia: A Case Report. [PDF]
Clin Case RepABSTRACT Follicular porokeratosis (FPK) is a rare subtype of porokeratosis. Follicular porokeratosis mainly occurs in men and may be localized or diffuse. Involvement of the scalp is rarely reported, and we found only one case of alopecia due to scalp FPK.
Abdolvand M +4 more
europepmc +2 more sources
Disseminated superficial porokeratosis
Dermatology Online Journal, 2010 A 62-year-old woman with psoriasis and psoriatic arthritis presented for evaluation and treatment of a one-week history of pruritic, pink spots on her trunk and extremities. Several weeks prior, therapy with certolizumab pegol and methotrexate was started for her psoriatic arthritis. A biopsy specimen was consistent with the diagnosis of porokeratosis.
Brauer, Jeremy A +5 more
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From a Gene Mutation to Pathology and Targeted Therapy in a Patient with Therapy-resistant Porokeratosis [PDF]
Acta Dermato-VenereologicaMelina Möller +4 more
doaj +2 more sources
Autosomal dominant genodermatoses in adults being heralded by superimposed skin lesions in children
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Volume 193, Issue 2, Page 109-115, June 2023., 2023 Abstract In autosomal dominant skin disorders, pronounced mosaic involvement may sometimes occur in the neonate, originating in a heterozygous embryo from early loss of heterozygosity, probably during the first week after fertilization. In biallelic phenotypes, such overlaying mosaic involvement may coexist with disseminated mosaicism, for example, in ...
Rudolf Happle
wiley +1 more source
Porokeratosis plantaris palmaris et disseminata with pruritic inflammatory changes
JEADV Clinical Practice, Volume 2, Issue 2, Page 366-368, June 2023., 2023 Abstract Porokeratosis plantaris palmaris et disseminata (PPPD) is a rare variant of porokeratosis that begins on the palms and soles and subsequently spreads to the trunk and extremities. We report a case of PPPD with pruritic inflammatory changes in a 48‐year‐old man, presenting with a 3‐year history of pruritic papules that initially appeared on his
Kei Hayashi +2 more
wiley +1 more source
Anais Brasileiros de Dermatologia, 2010 As poroceratoses compreendem um grupo de doenças da queratinização epidérmica, hereditárias ou adquiridas, caracterizadas histologicamente pela presença de lamela cornoide.
Tiago Torres +2 more
doaj +1 more source
Porokeratoses – all in one: A coexistence of clinical variants
Clinical Dermatology Review, 2022 Porokeratosis (PK) is an autosomal dominant disorder characterized by abnormal epidermal proliferation. Several clinical variants have been described, but coexistence of multiple variants in a single patient has been reported in only a few cases.
Kalgi Baxi +5 more
doaj +1 more source
Disseminated superficial "actinic" porokeratosis
Acta Dermato-Venereologica, 1979 An 81-year-old Finnish female had a 10-month history of a very pruritic eruption. In the clinical examination porokeratosis was suspected and histologically verified with the typical cornoid lamellae. The eruption involved also the unexposed areas of the skin. The patient had always avoided sunshine because it made her feel uncomfortable. The patient's
A L, Kariniemi, M L, Kotovirta, S, Stubb
openaire +2 more sources
Porokeratosis ptychotropica: a rare manifestation with typical histological exam [PDF]
Anais Brasileiros de Dermatologia, 2016 : Porokeratosis is a disorder of epidermal keratinization characterized clinically by a distinctive ridge-like border, and histologically by cornoid lamellae.
John Verrinder Veasey +5 more
doaj +2 more sources