Results 41 to 50 of about 1,856 (171)
Atypical Follicular–Pigmentary Variant of Hailey–Hailey Disease: A Diagnostic Dilemma
ABSTRACT Hailey–Hailey disease (HHD) is a rare autosomal dominant acantholytic dermatosis characterized by recurrent erosive plaques in intertriginous areas. Atypical presentations can resemble other acantholytic disorders, making diagnosis challenging. A 38‐year‐old male presented with recurrent pruritic lesions over flexural regions, worsened by heat
Sandesh Shah +5 more
wiley +1 more source
A Case of Darier‐Roussy Sarcoidosis Mimicking Rheumatoid Nodule
ABSTRACT Darier‐Roussy sarcoidosis is a rare cutaneous sarcoidosis presenting with painless subcutaneous nodules and minimal systemic involvement. A 58‐year‐old Ethiopian man developed symmetrical nodules mimicking rheumatoid nodules. Histology confirmed non‐caseating granulomas.
Milion Gebrewold Abdi +6 more
wiley +1 more source
Type one segmental Darier′s disease
A 50-year-old woman presented with multiple pruritic hyperpigmented papules in a zosteriform pattern involving the abdomen and back on the left side and in a linear pattern involving the left arm and forearm of 2 years duration.
Arunprasath Palanisamy +3 more
doaj +1 more source
Biomolecular Changes Upon Ablative Laser Therapy of the Skin: A Scoping Review
(Fractional) ablative laser therapy results in a wound healing response characterized by an inflammatory phase, dermal matrix degradation, and remodeling, collagenesis and elastogenesis. This is characterized by an increase in metalloproteinases, collagen type I, III, VII, and tropoelastin.
Marie‐Eline Pauline Henriette Debeuf +4 more
wiley +1 more source
ABSTRACT Introduction Hailey‐Hailey disease (HHD) is a rare genodermatosis caused by mutations in the ATP2C1 gene that codes for SPCA1, a calcium transporter in the epidermis. HHD impairs quality of life, and no curative treatment exists. Methods To confirm the efficacy and safety of CO2 laser in HHD, we conducted a randomized, prospective, controlled ...
Javier Antoñanzas +7 more
wiley +1 more source
Treatment of Darier’s disease with oral magnesium: a case report
Darier’s disease, an autosomal dominant genodermatosis, arises from a mutation in the ATP2A2 gene that codes for sarco/endoplasmic reticulum Ca 2+ -ATPase in the endoplasmic reticulum and is characterized by greasy keratotic papules commonly found in ...
Heidi Oi-Yee Li +2 more
doaj +1 more source
Darier-White disease: A rare genetic disorder [PDF]
Background: The clinical manifestation of Darier-White disease, an autosomal dominant genodermatosis, are greasy hyperkeratotic papules in seborrheic regions with nail abnormalities and mucous membrane changes due to a defective sarcoendoplasmic calcium ...
Cara Lynn Marie N. Chia +3 more
doaj +1 more source
Encorafenib‐associated acantholytic dermatosis in collision with eccrine squamous syringometaplasia
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Francisco Meraz‐Torres +5 more
wiley +1 more source
Dermatology 2.0: Precision medicine for inflammatory skin diseases
Digital immune mapping of transcriptomics profiles from inflammatory skin disease biopsies enables precise molecular diagnosis, quantification of immune modules and personalized therapy selection by matching dominant immune signatures to targeted treatments.
Jeremy Di Domizio +4 more
wiley +1 more source
Darier-White disease of the vulva. Presentation of a patient
The Darier-White disease is an uncommon genodematoses, the transmisision of autosomal dominant, characterized by lesions involving papulokeratosic mucosal and nails; may appear papules on the vulva, specifically.
Mabel González Escudero +2 more
doaj

