Results 21 to 30 of about 2,122 (187)

A case of disseminated superficial porokeratosis associated with giant porokeratosis in pregnancy

open access: yesIndian Journal of Dermatology, 2014
A 23-year-old pregnant lady presented with dark raised lesions over face, axillae, and upper limbs of 15-day duration. She was 35 weeks pregnant at the time of onset of the lesions.
Biju Vasudevan   +4 more
doaj   +2 more sources

MVD Variants Identified in a Rare Clinical Variant of Porokeratosis: A Case Report of Disseminated Superficial Porokeratosis (DSP) in a Chinese Patient

open access: yesClinical, Cosmetic and Investigational Dermatology
Tao Yu,1 Yue Yin,1 Chang Shu,2 Cheng-da Yuan1 1Department of Dermatology, Hangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, Zhejiang, People’s Republic of China; 2Department of Pathology, Hangzhou TCM Hospital Affiliated ...
Yu T, Yin Y, Shu C, Yuan CD
doaj   +2 more sources

A Case of Linear Porokeratosis Superimposed on Disseminated Superficial Actinic Porokeratosis

open access: yesCase Reports in Dermatology, 2010
We present a female patient with linear porokeratosis of her right arm since childhood. At the age of 67 years she additionally developed disseminated superficial actinic porokeratosis (DSAP) involving both lower legs.
Rebecca Löhrer   +7 more
doaj   +2 more sources

A Case Report of Inflammatory Disseminated Superficial Porokeratosis: An Eruptive Pruritic Papular Variant of Porokeratosis

open access: yesInternational Journal of Dermatology and Venerology, 2021
. Introduction:. Eruptive pruritic papular porokeratosis (EPPP) is a rare variant of porokeratosis. Several cases of this varient of porokeratosis had been reported.
Ling-Ling Luo   +3 more
doaj   +1 more source

Eruptive pruritic papular porokeratosis or inflammatory form of disseminated superficial porokeratosis: a new case and review of the literature [PDF]

open access: yes, 2020
Porokeratosis is a heterogeneous group of dermatoses with alterations of keratinization. Histologically, they are characterized by the presence of cornoid lamellae.
Feola, Hernán   +2 more
core   +1 more source

A case of squamous cell carcinoma arising in a giant porokeratosis previously diagnosed as psoriasis

open access: yesDermatology Reports, 2022
Porokeratosis (PK) is a disorder of keratinization with a clinical presentation of an atrophic center surrounded by a hyperkeratotic border. Lesions of porokeratosis carry a risk of malignant transformation with giant porokeratosis (GPK) being a high ...
Lorry Aitkens   +3 more
doaj   +1 more source

Focal actinic porokeratosis: A new variant?

open access: yesIndian Journal of Paediatric Dermatology, 2018
Porokeratosis is an autosomal dominantly transmitted disorder of keratinization predominantly affecting trunk and extremities. Many clinical variants have been described having a common histopathological feature of coronoid lamella-porokeratosis of ...
Pihu Sethi   +3 more
doaj   +1 more source

Treating linear porokeratosis with topical lovastatin/cholesterol cream [PDF]

open access: yes, 2022
Linear porokeratosis is a rare variant of porokeratosis that is characterized by unilateral lesions along the lines of Blaschko. Like all variants of porokeratosis, linear porokeratosis is characterized by the histopathologic finding of cornoid lamellae ...
Buhle, Anna C   +3 more
core   +1 more source

Porokeratosis ptychotropica: Dermoscopy, reflectance confocal microscopy, and histopathological correlation

open access: yesIndian Journal of Dermatology, 2021
Porokeratosis ptychotropica (PP) is a rare variant of porokeratosis characterized by pruritic, symmetrical, red-brown verrucous papules, and plaques most commonly localized within the gluteal fold.
Francesco Lacarrubba   +5 more
doaj   +1 more source

Porokeratosis of Mibelli - literature review and a case report [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2013
Porokeratosis is a disorder of epidermal keratinization characterized by annular plaques with an atrophic center and hyperkeratotic edges, and includes a heterogeneous group of disorders that are mostly inherited in an autosomal dominant form.
Flávia Regina Ferreira   +3 more
doaj   +1 more source

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