Results 41 to 50 of about 685 (153)
This article aimed to evaluate the efficacy and safety of JAK1 inhibitors (abrocitinib and upadacitinib) in off‐label treatment of refractory inflammatory skin diseases. We retrospectively analyzed 19 patients with various immune‐mediated dermatoses, including cutaneous lichen planus, parapsoriasis, vitiligo, autoimmune bullous diseases ...
Si Zhang +5 more
wiley +1 more source
Molecular characterization and natural history of linear porokeratosis: a case series
Here we employed immunohistochemistry and genetic testing by whole-exome or Sanger sequencing, to characterize six cases with linear porokeratosis (LP), all having negative family history for porokeratosis (Table 1).
saleva, M (via Mendeley Data)
core +1 more source
Background and Objective Porokeratosis comprises a heterogeneous group of keratinization disorders with malignant transformation potential. While multiple therapeutic options exist, clinical outcomes remain suboptimal. Emerging evidence suggests promising efficacy of topical statin therapy, though systematic evaluation is currently lacking.
Xingyu Li +3 more
wiley +1 more source
Porokeratosis ptychotropica: a rare case report with unusual presentation
Porokeratosis is a rare disorder of epidermal keratinization characterized clinically by annular plaque with thread like hyperkeratotic border with a central groove that expand centrifugally and this border corresponds to coronoid lamellae histologically
N., Azeem Jaffer +2 more
core +1 more source
ABSTRACT Intralesional bleomycin is an effective and safe treatment option for plantar mosaic warts that are resistant to conventional therapies. This case highlights the importance of targeted intralesional therapy, even in recalcitrant and extensive plantar wart variants, with rapid resolution observed after just two treatment sessions and no ...
Amrit Neupane +3 more
wiley +1 more source
ABSTRACT Mosaicism due to postzygotic mutations is more common than considered before the era of massive parallel sequencing. In the clinical dermatologic practice, it is important to recognize skin lesions and syndromes caused by genetic mosaicism, to initiate genetic testing and counsel the patient and families regarding prognosis and risk of ...
Cristina Has
wiley +1 more source
A Long‐Standing Palmar Depressed Macule
JEADV Clinical Practice, Volume 5, Issue 2, Page 734-736, June 2026.
Jhon Edwin Rodríguez‐Vásquez +4 more
wiley +1 more source
Categories of Cutaneous Mosaicism
ABSTRACT In this overview, the following 12 different categories of cutaneous mosaicism are considered: (1) Discrimination between monoallelic and biallelic mosaicism in autosomal dominant traits; (2) Segmental versus disseminated mosaicism in autosomal dominant disorders.
Rudolf Happle
wiley +1 more source
Linear porokeratosis: a case report [PDF]
Abstract Porokeratosis is a rare genodermatosis based on chronic keratinization disorder histologically characterized by the presence of a cornoid lamella and various clinical manifestations. Five most commonly described types of poroketarosis are porokeratosis of Mibelli or ”classic” porokeratosis, disseminated superfi cial actinic porokeratosis,
Slobodan Stojanović +3 more
openaire +1 more source

