Results 121 to 130 of about 1,529 (176)

Penile Porokeratoma: A Case Report. [PDF]

open access: yesIndian Dermatol Online J
Gaurav V, Agarwal D, Mandal S, Yadav D.
europepmc   +1 more source

Ultraviolet-Induced Fluorescence Dermoscopy of Porokeratosis. [PDF]

open access: yesIndian Dermatol Online J
Sankar PA, Khare S, Ganguly S.
europepmc   +1 more source

Photosensitive symmetric papules of the nasal alae. [PDF]

open access: yesJAAD Case Rep
Peng DS   +4 more
europepmc   +1 more source

Porokeratosis

JAMA Dermatology, 2023
This case report describes multiple, hyperpigmented plaques involving the face, trunk, and bilateral upper and lower extremities.
Ishika, Muradia   +2 more
openaire   +2 more sources

Porokeratosis ptychotropica: a rare and evolving variant of porokeratosis

Journal of Cutaneous Pathology, 2013
Porokeratosis ptychotropica represents a rare and under‐recognized variant of porokeratosis. There are also alternative descriptions for this disorder in the literature. Since its original description in 1995, additional characteristic features have been showed in case reports published in the literature.
Ben Tallon
exaly   +3 more sources

Follicular Porokeratosis, a Porokeratosis Variant

The American Journal of Dermatopathology, 2017
Abstract: Porokeratosis derives from a process of abnormal keratinization, resulting in clinical and histologic variants. Follicular involvement is infrequently described, with previous suggestions that it may represent a distinct condition.
Ben, Tallon, Patrick, Emanuel
openaire   +2 more sources

Linear Porokeratosis

The Journal of Dermatology, 1993
AbstractA case of linear porokeratosis in a 14‐year‐old girl was reported. The lesions started from the right forearm and extended to the right breast. Histological examinations showed cornoid lamella in the horny layer and dyskeratotic cells in the spinous layer beneath the cornoid lamella.
Y, Taniguchi, T, Yuasa, M, Shimizu
openaire   +2 more sources

Porokeratosis and immunosuppression

British Journal of Dermatology, 1995
Immunosuppression may favour the development of disseminated superficial porokeratosis (DSP). We report the clinical features and the outcome of DSP in 24 patients receiving immunosuppressive treatment (group A), and compare the characteristics of the disease with those of 13 immunocompetent patients with DSP (group B). The two groups were similar with
P L, Bencini   +4 more
openaire   +2 more sources

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