Assuntos
Infecções Oportunistas Relacionadas com a AIDS/diagnóstico , Infecções por Citomegalovirus/diagnóstico , Infecções por HIV/complicações , Polirradiculopatia/etiologia , Tuberculose Meníngea/etiologia , Infecções Oportunistas Relacionadas com a AIDS/tratamento farmacológico , Adulto , Antituberculosos/uso terapêutico , Antivirais/uso terapêutico , Encéfalo/diagnóstico por imagem , Infecções por Citomegalovirus/tratamento farmacológico , Diagnóstico Diferencial , Foscarnet/uso terapêutico , Infecções por HIV/tratamento farmacológico , Humanos , Região Lombossacral , Imageamento por Ressonância Magnética , Masculino , Polirradiculopatia/diagnóstico , Polirradiculopatia/tratamento farmacológico , Inibidores da Transcriptase Reversa/uso terapêutico , Tomografia Computadorizada por Raios X , Tuberculose dos Linfonodos/tratamento farmacológico , Tuberculose dos Linfonodos/etiologia , Tuberculose Meníngea/diagnóstico , Tuberculose Meníngea/tratamento farmacológicoRESUMO
The Neutrophilic dermatosis (ND) is considered as an independent entity with diverse clinical manifestations among which there are: gangrenous pyoderma, nodous erythema, Sweets Syndrome, vesiculopustula eruptions associated to ulcerous colitis and intestinal short circuit syndrome with or without short circuit. Histologically, they are characterized by infiltration of polymorphonuclear neutrophils, generally at the dermic level, but also at the epidermic. They are usually associated to systemic diseases, especially to chronic intestinal inflammatory disease. Our aim was to describe two forms of clinical presentation of neutrophilic dermatosis: gangrenous pyoderma and vesiculopustula eruption, associated to ulcerous colitis starting at advances ages.
Assuntos
Colite Ulcerativa/complicações , Neutrófilos , Dermatopatias/etiologia , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Pessoa de Meia-Idade , Dermatopatias/patologiaRESUMO
A 42 year old female, diagnosed as having Sweet's syndrome, is presented as a new case of this rare disease (less than 100 cases reported before 1985) and the literature of the syndrome is reviewed. The clinical and histological features and its association with other diseases, especially the pathogenesis and treatment, are commented on.