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2.
Ann Dermatol Venereol ; 133(2): 145-7, 2006 Feb.
Artigo em Francês | MEDLINE | ID: mdl-16508598

RESUMO

INTRODUCTION: Drug hypersensitivity syndrome is a severe life-threatening drug reaction. An association between this syndrome and HHV6 reactivation has been hypothesized. CASE-REPORT: A 45 year-old women was treated with sulfasalazine for polyarthralgia. One month after beginning the treatment, she developed a drug hypersensitivity syndrome with severe acute hepatic failure. HHV6 serology and serum PCR revealed a primary HHV6 infection. DISCUSSION: We report the second case of drug hypersensitivity syndrome associated with a primary HHV6 infection. An immunological disorder may explain such an association by increasing viral replication. Detection and titration of anti-HHV6 antibodies in each case of drug hypersensitivity syndrome should help to confirm this association and possibly modify treatment strategy.


Assuntos
Antirreumáticos/efeitos adversos , Doença Hepática Induzida por Substâncias e Drogas/etiologia , Toxidermias/complicações , Toxidermias/etiologia , Hipersensibilidade a Drogas/complicações , Herpesvirus Humano 6 , Infecções por Roseolovirus/complicações , Sulfassalazina/efeitos adversos , Corticosteroides/administração & dosagem , Corticosteroides/uso terapêutico , Doença Hepática Induzida por Substâncias e Drogas/complicações , Doença Hepática Induzida por Substâncias e Drogas/tratamento farmacológico , Hipersensibilidade a Drogas/etiologia , Feminino , Humanos , Pessoa de Meia-Idade , Síndrome , Fatores de Tempo , Resultado do Tratamento
3.
Dermatology ; 205(1): 60-2, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12145437

RESUMO

We report a localized form of lymphomatoid papulosis (LyP) presenting as pustular papules of the hands. The histopathology revealed a moderate inflammatory infiltrate composed of atypical pleomorphic large lymphocytes with atypical mitosis and large nuclei. Epidermotropism could be observed. These atypical cells expressed CD4 and CD30. Laboratory examinations and bone marrow explorations remained negative. The clinical presentation of this case of LyP is unusual. Only histopathological features allowed to diagnose LyP. The knowledge that LyP may be associated with neoplasia or lymphoma underlines the need for a long-term follow-up of these patients.


Assuntos
Dermatoses da Mão/patologia , Papulose Linfomatoide/patologia , Humanos , Masculino , Pessoa de Meia-Idade , Pele/patologia
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