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A Report of Eruptive Pruritic Papular Porokeratosis Treated with Abrocitinib
Jiali Xia, Guan Jiang Department of Dermatology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, 221002, People’s Republic of ChinaCorrespondence: Guan Jiang, Department of Dermatology, The Affiliated Hospital of Xuzhou Medical University ...
Guan Jiang
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JAMA Dermatology, 2023
This case report describes multiple, hyperpigmented plaques involving the face, trunk, and bilateral upper and lower extremities.
Ishika, Muradia +2 more
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This case report describes multiple, hyperpigmented plaques involving the face, trunk, and bilateral upper and lower extremities.
Ishika, Muradia +2 more
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Follicular Porokeratosis, a Porokeratosis Variant
The American Journal of Dermatopathology, 2017Abstract: 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
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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
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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
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SKINmed: Dermatology for the Clinician, 2008
A 34‐year‐old man from El Salvador was referred to our clinic with a 10‐year history of a pruritic erythematous facial eruption. He reported increased pruritus and scaling of lesions when exposed to the sun. He worked as a construction worker and admitted to frequent sun exposure.
Dafnis C, Carranza +2 more
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A 34‐year‐old man from El Salvador was referred to our clinic with a 10‐year history of a pruritic erythematous facial eruption. He reported increased pruritus and scaling of lesions when exposed to the sun. He worked as a construction worker and admitted to frequent sun exposure.
Dafnis C, Carranza +2 more
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Clinical and Experimental Dermatology
A 48-year-old woman with an otherwise clear past medical history presented with pink-to-brown pruritic plaques on sun-exposed areas, including the hands and torso, which started 5 years previously. She was otherwise well. Similar lesions on sun-exposed areas were also present in her son and mother.
Andrew Awad +3 more
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A 48-year-old woman with an otherwise clear past medical history presented with pink-to-brown pruritic plaques on sun-exposed areas, including the hands and torso, which started 5 years previously. She was otherwise well. Similar lesions on sun-exposed areas were also present in her son and mother.
Andrew Awad +3 more
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Porokeratosis and immunosuppression
British Journal of Dermatology, 1995Immunosuppression 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
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Archives of Dermatology, 1969
To the Editor.— In their otherwise outstanding paper in the December 1968,Archives, Woodside et al (page 651) refer to the palmar lesions of the basal cell nevus syndrome as "porokeratosis of Mantoux." This term has also been associated with the basal cell nevus syndrome by Calnan ( British Journal of Dermatology 65 :219, 1953).
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To the Editor.— In their otherwise outstanding paper in the December 1968,Archives, Woodside et al (page 651) refer to the palmar lesions of the basal cell nevus syndrome as "porokeratosis of Mantoux." This term has also been associated with the basal cell nevus syndrome by Calnan ( British Journal of Dermatology 65 :219, 1953).
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British Journal of Dermatology, 1991
A 63-year-old man developed linear, annular and accuminate lesions which showed the histological features of porokeratosis. The lesions cleared spontaneously, recurred several months later and ulcerated, then cleared again. The spontaneous resolution and recurrence of the lesions is a hitherto undescribed pattern of porokeratosis.
B, Adriaans, J R, Salisbury
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A 63-year-old man developed linear, annular and accuminate lesions which showed the histological features of porokeratosis. The lesions cleared spontaneously, recurred several months later and ulcerated, then cleared again. The spontaneous resolution and recurrence of the lesions is a hitherto undescribed pattern of porokeratosis.
B, Adriaans, J R, Salisbury
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International Journal of Dermatology, 2004
Porokeratosis is a disorder of keratinization characterized by annular plaques with an atrophic center surrounded by a raised, keratotic wall. It has several clinical forms including a porokeratosis of Mibelli, giant porokeratosis, linear porokeratosis, disseminated superficial actinic porokeratosis, palmoplantar porokeratosis and punctate ...
Kübra Eren, Bozdağ +2 more
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Porokeratosis is a disorder of keratinization characterized by annular plaques with an atrophic center surrounded by a raised, keratotic wall. It has several clinical forms including a porokeratosis of Mibelli, giant porokeratosis, linear porokeratosis, disseminated superficial actinic porokeratosis, palmoplantar porokeratosis and punctate ...
Kübra Eren, Bozdağ +2 more
openaire +2 more sources

