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1.
Dermatol Online J ; 25(3)2019 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-30982306

RESUMO

Grover disease (GD) is a disorder of unknown origin, clinically characterized by the occurrence of pruritic, erythematous or brownish papules and papulovesicles, which histologically reveal four different patterns of acantholysis. Usually, the eruption is self-limited and spontaneously remit within a few weeks. In some cases, however, it may persist for months or even years and show a therapy-resistant course. We report a 56-year-old woman with recalcitrant, persistent, and generalized GD who showed complete remission after 6 weeks of treatment with oral acitretin (0.8mg/kg/day). The treatment was well-tolerated and laboratory parameters remained unchanged. The patient remains free of any recurrence at 26 months. To the best of our knowledge, this is the first report of a complete remission of the persistent form of GD as a result of oral acitretin monotherapy.


Assuntos
Acantólise/tratamento farmacológico , Acitretina/uso terapêutico , Ictiose/tratamento farmacológico , Ceratolíticos/uso terapêutico , Acantólise/patologia , Feminino , Humanos , Ictiose/patologia , Pessoa de Meia-Idade , Indução de Remissão
2.
Breast J ; 19(2): 193-5, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23294250

RESUMO

Lynch Syndrome, an autosomal dominantly inherited cancer predisposition syndrome is not typically associated with development of breast cancer. We present two cases of loss of mismatch protein expression in breast cancer cases in patients with Lynch Syndrome and discuss the literature surrounding the subject.


Assuntos
Neoplasias da Mama/genética , Neoplasias Colorretais Hereditárias sem Polipose/genética , Proteínas de Ligação a DNA/genética , Proteína 2 Homóloga a MutS/genética , Proteínas Adaptadoras de Transdução de Sinal/genética , Adulto , Idoso de 80 Anos ou mais , Neoplasias Colorretais Hereditárias sem Polipose/cirurgia , Feminino , Regulação Neoplásica da Expressão Gênica , Humanos , Masculino , Proteína 1 Homóloga a MutL , Proteínas Nucleares/genética
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