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2.
Dermatologica ; 170(2): 86-9, 1985.
Artigo em Inglês | MEDLINE | ID: mdl-3884401

RESUMO

3 patients with multiple sclerosis (MS) who developed severe widespread bullous pemphigoid (BP) are presented. MS preceded the presentation of BP by 13-23 years (mean 18 years). BP was confirmed histologically and immunopathologically. Upon successful therapy with steroids, no recurrence of BP was observed over a 3-5 year (mean 3.7 years) follow-up. Several abnormalities of the immune system have been reported in both diseases. It is interesting to speculate that amidst existing immunologic abnormalities in all 3 patients with MS, a specific event, immunologic or viral or both may have triggered the development of BP.


Assuntos
Esclerose Múltipla/complicações , Penfigoide Bolhoso/complicações , Dermatopatias Vesiculobolhosas/complicações , Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Esclerose Múltipla/imunologia , Penfigoide Bolhoso/imunologia
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