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2.
Actas dermo-sifiliogr. (Ed. impr.) ; 108(7): e49-e52, sept. 2017. ilus, tab
Article in Spanish | IBECS | ID: ibc-166939

ABSTRACT

La enfermedad de Darier es una genodermatosis autosómica dominante, que se produce por la mutación de un gen, que produce una proteína que interviene en la regulación de los canales de calcio; presenta distintas manifestaciones clínicas y falta de consistencia genotipo/fenotipo. La variante acral hemorrágica se caracteriza por máculas, pápulas, vesículas y/o ampollas hemorrágicas en zonas acrales, puede asociar otras manifestaciones clásicas de la enfermedad de Darier en el mismo paciente o sus familiares; en la histopatología se evidencia disqueratosis y acantólisis suprabasal con formación de lagunas hemorrágicas. Reportamos 3 nuevos casos de esta variante desencadenados por traumatismo y evidenciando buena respuesta con retinoides (AU)


Darier disease is an autosomal-dominant inherited condition caused by mutation of a gene, which produces a protein involved in calcium channel regulation. The disease has a variety of manifestations and lacks consistent genotype-phenotype correlations. Acral hemorrhagic Darier disease causes macules, papules, vesicles and/or hemorrhagic blisters on the extremities. Other classic signs of the disease may be present in the same patient or relatives. Histopathology reveals dyskeratosis and suprabasal acantholysis with hemorrhagic lacunae. We report 3 new cases of this type of Darier disease triggered by injuries. Response to retinoid therapy was good (AU)


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Darier Disease/diagnosis , Hemorrhagic Disorders/etiology , Dyskeratosis Congenita/diagnosis , Acantholysis/diagnosis , Genetic Markers/genetics , Genetic Predisposition to Disease
3.
Actas Dermosifiliogr ; 108(7): e49-e52, 2017 Sep.
Article in English, Spanish | MEDLINE | ID: mdl-28407871

ABSTRACT

Darier disease is an autosomal-dominant inherited condition caused by mutation of a gene, which produces a protein involved in calcium channel regulation. The disease has a variety of manifestations and lacks consistent genotype-phenotype correlations. Acral hemorrhagic Darier disease causes macules, papules, vesicles and/or hemorrhagic blisters on the extremities. Other classic signs of the disease may be present in the same patient or relatives. Histopathology reveals dyskeratosis and suprabasal acantholysis with hemorrhagic lacunae. We report 3 new cases of this type of Darier disease triggered by injuries. Response to retinoid therapy was good.


Subject(s)
Darier Disease/etiology , Hand Injuries/complications , Acitretin/therapeutic use , Adult , Darier Disease/drug therapy , Darier Disease/genetics , Darier Disease/pathology , Dermatologic Agents/therapeutic use , Female , Humans , Isotretinoin/therapeutic use , Male , Middle Aged , Nails, Malformed/etiology , Sarcoplasmic Reticulum Calcium-Transporting ATPases/genetics , Seasons , Tretinoin/therapeutic use
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