Results 1 to 10 of about 438 (140)

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

Indian 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, Manas Chatterjee, Rajan Grewal, Vandana Rana, Nikita Lodha   +4 more
doaj   +4 more sources

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

Clinical, 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   +4 more sources

Disseminated Superficial Actinic Porokeratosis

Nepal Journal of Dermatology, Venereology & Leprology, 2012
A Case Report about a rare Geno dermatosis -Dissamenated Superficial Actinic Porokeratosis is presented. Key Words: Classic porokeratosis of Mibelli (PM); disseminated superficial actinic porokeratosis (DSAP); porokeratosis palmaris et plantaris ...
S Kumari, M Mathur
doaj   +11 more sources

A rare case of disseminated superficial porokeratosis-Case report [PDF]

Journal of Family Medicine and Primary Care, 2022
Porokeratosis is a keratinization disorder characterized by hyperkeratotic sharply demarcated plaques with central atrophy and histopathologically, by cornoid lamella.
Ramachandran Ramakrishnan, T Arun Vignesh, Priya Cinna T. Durai, Murali Narasimhan   +3 more
doaj   +2 more sources

Disseminated Superficial Porokeratosis: A Case Report. [PDF]

Cureus
Disseminated superficial porokeratosis is a rare dermatological disorder characterized by annular keratotic lesions, presenting diagnostic challenges due to its variable clinical manifestations. The pathogenesis involves genetic predisposition and environmental factors, with mutations in the mevalonate pathway implicated.
Taha A, Khormi G, Alali L, Maashi A, Alharbi A.   +4 more
europepmc   +3 more sources

A Case of Squamous Cell Carcinoma Arising in Disseminated Superficial Porokeratosis [PDF]

Clinical, Cosmetic and Investigational Dermatology
Hui-E Zheng, Yun Wang, Shuhui Wu, Ming-Fang Zhu Department of Dermatology, The Second Affiliated Hospital of Hunan University of Chinese Medicine, Changsha, People’s Republic of ChinaCorrespondence: Ming-Fang Zhu, Department of Dermatology, The Second ...
Zheng HE, Wang Y, Wu S, Zhu MF
doaj   +2 more sources

Disseminated Superficial Porokeratosis with Dermal Amyloid Deposits [PDF]

Case Reports in Dermatology, 2009
Only 6 cases with an association of disseminated superficial porokeratosis with dermal amyloid deposits are reported in the literature. We present the case of a 76-year-old woman who presented with a disseminated superficial porokeratosis.
M. Carlesimo, A. Rossi, L. Fidanza, A. Narcisi, M. La Pietra, E. Mari, C. Cacchi, G. Camplone   +7 more
doaj   +2 more sources

Porokeratoses—A Rare Group of Dermatoses [PDF]

Medicina
Porokeratoses represent a rare group of skin diseases characterized by abnormal keratinization. The condition may have a genetic background and can be triggered by environmental factors, including UV exposure and infections.
Agnieszka Anderska, Agnieszka Kaczmarska-Such, Ewelina Mazur, Adam Reich   +3 more
doaj   +2 more sources

Dermoscopy of Disseminated Superficial Actinic Porokeratosis

Actas Dermo-sifiliográficas, 2017
We present a series of 6 cases of disseminated superficial actinic porokeratosis and describe their dermoscopic features. Dermoscopy is a noninvasive in vivo technique that is useful as a tool for the diagnosis and follow-up of porokeratosis. This condition has specific dermoscopic features that were observed in our series of cases and that are ...
A, Nicola, J, Magliano
exaly   +3 more sources

Identification of two novel MVD mutations and one novel FDPS mutation in Chinese patients with porokeratosis [PDF]

Frontiers in Medicine
BackgroundPorokeratosis (PK) is an autosomal dominant inherited disorder characterized by abnormal epidermal keratinization, primarily resulting from mutations in four genes associated with the mevalonate pathway: mevalonate decarboxylase (MVD ...
Yang He, Shengcai Zhu, Quan Wei, Fan Ye, Yunxia Zhu, Xiaoliang Ouyang, Liang Wu, Chunming Li   +7 more
doaj   +2 more sources