Results 61 to 70 of about 2,122 (187)
JEADV Clinical PracticeBackground Porokeratoses represent a group of keratinization disorders characterized histopathologically by the presence of a cornoid lamella. The recognition of porokeratosis as a genodermatosis, along with its association with increased risk of skin ...
Rahime Inci +5 more
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Porokeratosis of the scrotum: a case report and literature review
Frontiers in MedicinePorokeratosis, a keratinizing disorder of unknown etiology, exhibits an autosomal dominant inheritance pattern or manifests as an isolated acquired dermatosis. This condition can occur at any site on the skin; however, scrotal lesions are extremely rare.
Xiaorong Zhang, Bangtao Chen, Jing Yang
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Linear porokeratosis over the face: An unusual presentation
Indian Journal of Paediatric Dermatology, 2016 Porokeratosis is a heterogeneous disorder of keratinization usually inherited in an autosomal dominant pattern. It usually affects the trunk and extremities. Lesions exclusively present over face are rare and not well-documented.
Dibyendu Basu +2 more
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Actas Dermo-Sifiliográficas (English Edition), 2008 Porokeratosis is a primary disorder of epidermal keratinization. The term covers several clinical variants that have in common the presence of a cornoid lamella in histological studies. Although porokeratotic lesions may appear anywhere on the skin, genital lesions are uncommon and may occur in cases of generalized porokeratosis with genital ...
openaire +2 more sources
, 2005 Porokeratosis is a specific disorder of keratinization that has five clinical types and shows a characteristic ′cornoid lamella′ on histopathology. Malignant degeneration has been described in all forms of porokeratosis.
Asok Gangopadhyay +2 more
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Porokeratosis of Mibelli induced by topical corticosteroid
, 2006 Background:Porokeratosis of Mibelli is a chronic disorder characterised by slightly atrophic plaques surrounded by keratotic border. Methods and Results:A 45-year-old man treated with clobetazole propionate ointment for psoriasis over 15 years developed ...
Kazandi, Ali Can +3 more
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Porokeratosis: immunosuppression and exposure to sunlight
, 1987 Four cases of disseminated superficial actinic porokeratosis are described, all in patients who had been given immunosuppressive treatment, which might have been a contributing factor in the development of the condition.
P. L. Bencini, F. Sala, C. Crosti
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, 1998 A case of linear porokeratosis in a 3 year old male child is reported for its rarity and clinical interest.
Ramanan Cherukot +2 more
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[Immunohistochemical study of porokeratosis in kidney transplantation]
, 1989 Six cases of disseminated actinic superficial porokeratosis are reported in kidney transplant recipients. Immunohistochemistry study showed an altered state of Langerhans cell surface markers at the level of the cutaneous lesions of porokeratosis. We can
Manganoni, A +3 more
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Clinical Case ReportsThis is the first documented case of disseminated superficial actinic porokeratosis (DSAP) successfully treated with topical ruxolitinib. The patient experienced near‐complete clearance after three months, suggesting that topical JAK inhibition may be an
Joe Khodeir +2 more
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