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Pediatr Dermatol ; 7(1): 42-7, 1990 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-1692995

RESUMO

Lymphomatoid papulosis (LyP) is rarely seen in children. We report a case of LyP in a 4-year-old boy in whom immunopathologic studies demonstrated T cell antigen deletions. In contrast to all but two previous reports, a T suppressor (CD-8) phenotype was predominant. Southern blot analysis of DNA isolated from a typical skin lesion indicated a clonal rearrangement of the T cell receptor beta gene. Because of a 10% frequency of malignant lymphomas in patients with LyP, long-term observation is crucial, especially in children. We recommend routine clonal rearrangement studies for aid in diagnosis and follow-up, and as possible prognostic indicators in children with this condition.


Assuntos
Epitopos/imunologia , Rearranjo Gênico do Linfócito T , Dermatopatias/imunologia , Linfócitos T/imunologia , Antígenos CD/imunologia , Southern Blotting , Criança , Pré-Escolar , Células Clonais , Feminino , Humanos , Lactente , Masculino , Receptores de Antígenos de Linfócitos T/genética , Dermatopatias/genética , Dermatopatias/patologia
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