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1.
Contact Dermatitis ; 82(5): 307-309, 2020 May.
Artículo en Inglés | MEDLINE | ID: mdl-31879957

RESUMEN

Patch tests are highly recommended in eczema patients with eyelid involvement. Sunscreen constitutes a potential cause of eyelid or facial allergic contact dermatitis, and should be considered in patients with refractory eczema on these locations. We report a patient sensitized to several emerging allergens such as bis-ethylhexyloxyphenol methoxyphenyl triazine (Tinosorb S), Scutellaria baicalensis extract, and propylene glycol with an eyelid dermatitis. Patch tests to the combined ingredients propylene carbonate, cyclopentasiloxane, and disteardimonium hectorite; and talc, Cl 77 491, and dimethicone/methicone copolymer were also positive. We highlight the importance of systematically patch testing with the cosmetics brought in by our patients, as well as with the individual ingredients whenever positive. The identification of emerging allergies to new compounds in cosmetics mainly depends on this practice.


Asunto(s)
Dermatitis Alérgica por Contacto/etiología , Enfermedades de los Párpados/inducido químicamente , Fenoles/efectos adversos , Extractos Vegetales/efectos adversos , Propilenglicol/efectos adversos , Triazinas/efectos adversos , Adulto , Femenino , Humanos , Pruebas del Parche , Scutellaria baicalensis
3.
Pediatr Dermatol ; 34(4): e205-e206, 2017 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-28425111

RESUMEN

Epidermolysis bullosa (EB) is a heterogeneous group of rare, chronic, inherited skin disorders characterized by marked mechanical fragility of epithelial tissues, with blistering and erosions after minor trauma. We present the first report of a nails-only phenotype in two patients with epidermolysis bullosa simplex (EBS) and a heterozygous pGlu170Lys mutation and the second reported case of EBS associated with a homozygous p.Glu170Lys mutation in the KRT5 gene. Our findings may be relevant for genetic counseling and for understanding the inheritance pattern of EBS.


Asunto(s)
Epidermólisis Ampollosa Simple/genética , Queratina-5/genética , Uñas/patología , Adulto , Niño , Femenino , Humanos , Masculino , Mutación , Fenotipo
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