Results 21 to 30 of about 1,529 (176)

Porokeratosis

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.
Sathe NC, Fillman EP.
europepmc   +3 more sources

Follicular porokeratosis at alae nasi; A case report and short review of literature

Indian Journal of Dermatology, 2014
Porokeratosis are disorders of keratinization, characterized histologically by a parakeratotic column, the cornoid lamellae, and clinically by a distinct peripheral ridge.
Emine Nur Rifaioglu, Gülzade Özyalvaçlı   +1 more
doaj   +1 more source

Long‐term disease control of disseminated superficial actinic porokeratosis (DSAP) with simvastatin 2%/ cholesterol 2% cream

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 7, Page 896-902, July 2026.
Summary Introduction Disseminated superficial actinic porokeratosis (DSAP) is a rare keratinization disorder associated with an increased risk of cutaneous tumors. Objectives To develop a feasible and easy‐to‐apply treatment regimen for long‐time disease control of DSAP including prevention of new skin tumors. Patients and Methods 19 patients with DSAP
Berenice M. Lang, Gregor Ojak, Mandy Crummenauer, Joanna Wegner, Caroline Mann, Stephan Grabbe, Petra Staubach   +6 more
wiley   +1 more source

Langanhaltende Krankheitskontrolle der disseminierten superfiziellen aktinischen Porokeratose (DSAP) mittels topischer Anwendung von 2% Simvastatin/2% Cholesterin‐Creme

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 7, Page 896-904, July 2026.
Zusammenfassung Einleitung Die disseminierte superfizielle aktinische Porokeratose (DSAP) ist eine seltene Keratinisierungsstörung, die mit einem erhöhten Risiko für kutane Tumoren verbunden ist. Zielsetzung Ziel der Studie war die Entwicklung eines praktikablen und einfach anwendbaren Behandlungsregimes für die langfristige Kontrolle der DSAP ...
Berenice M. Lang, Gregor Ojak, Mandy Crummenauer, Joanna Wegner, Caroline Mann, Stephan Grabbe, Petra Staubach   +6 more
wiley   +1 more source

Genital porokeratosis

Dermatology Online Journal, 2009
A 22-year-old man presented with a two-year history of warts on the penis, scrotum, and thighs. Physical examination showed multiple annular plaques with thin, threadlike borders on the penis and scrotum. The biopsy specimen showed a cornoid lamella with underlying dyskeratotic cells that was consistent with porokeratosis.
Liang, Christine, Batra, Priya, Patel, Rishi, Kamino, Hideko   +3 more
openaire   +4 more sources

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

Anais 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, Leopoldo Duailibe Nogueira Santos, Fernando Augusto Nogueira Mendes Tagliarini, Marcia Lanzoni de Alvarenga Lira   +3 more
doaj   +1 more source

Identification of an interstitial 18p11.32-p11.31 duplication including the EMILIN2 gene in a family with porokeratosis of Mibelli. [PDF]

PLoS ONE, 2013
Porokeratosis is a rare disease of epidermal keratinization characterized by the histopathological feature of the cornoid lamella, a column of tightly fitted parakeratocytic cells, whose etiology is still unclear. Porokeratosis of Mibelli is a subtype of
Corrado Occella, Dario Bleidl, Paolo Nozza, Samantha Mascelli, Alessandro Raso, Giorgio Gimelli, Stefania Gimelli, Elisa Tassano   +7 more
doaj   +1 more source

Carrier screening in the reproductive setting—Are there medical implications for the heterozygote?—A guide for clinicians

Pregnancy, Volume 2, Issue 3, May 2026.
Abstract Carrier screening for genetic conditions performed preconception or during pregnancy allows identification of fetal risk for inherited autosomal recessive and X‐linked conditions. The goal is to identify at‐risk patients/couples and offer them reproductive options such as preimplantation genetic diagnosis, prenatal testing, or targeted newborn
Emily B. Rosenfeld, Nicole Kasatkin, Bi Liu Yu, Milen Velinov, Justin S. Brandt, Elena Ashkinadze   +5 more
wiley   +1 more source

A Multifaceted Holistic Review of the Literature on Scar Dermatoses

International Wound Journal, Volume 23, Issue 5, May 2026.
ABSTRACT Many cutaneous diseases originate or manifest in scars. Scars are areas of compromised skin, which renders them a vulnerable cutaneous district for diseases to develop. The pathophysiology explaining why some dermatoses grow in scars is not yet thoroughly explored. The present study reviews the present literature on scar dermatoses.
Dana Maria Khoury, Elias El Tayar, Edward Eid, Firas F. Haddad, Ossama Abbas, Mazen Kurban   +5 more
wiley   +1 more source

Porokeratoses—A Rare Group of Dermatoses

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   +1 more source