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Folia Histochem Cytobiol ; 45(1): 21-5, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17378241

RESUMO

Langerhans cell histiocytoses (LCH) represent rare diseases of unclear etiology and pathogenesis. Most of the cases include children, 1 to 15 years of age, and various organs are involved (bones, skin, liver, lymph nodes, bone marrow and other). The diagnosis of LCH used to be established by biopsy of the inflamed tissue and demonstration of expression of markers specific for Langerhans cells: CD1a and langerin. The diagnosis can be ultimately confirmed by demonstration of Birbeck's granules in the electron microscopy. The present study was aimed at immunocytochemical demonstration, in the examined LCH material (skin, bones, lymph nodes), of the specific antigen expression and at comparing it with the presence of Birbeck's granules. In the examined 11 cases co-expression of CD1a with langerin and with the presence of Birbeck's granules was noted. Also in all examined biopsies the expression of S-100 protein on inflammatory cells was found. The results corroborate the usefulness of immunocytochemical studies on CD 1 a and langerin expression in diagnosis of LCH.


Assuntos
Antígenos CD1/metabolismo , Antígenos CD/metabolismo , Histiocitose de Células de Langerhans/diagnóstico , Imuno-Histoquímica , Células de Langerhans/imunologia , Lectinas Tipo C/metabolismo , Lectinas de Ligação a Manose/metabolismo , Adolescente , Antígenos CD1/imunologia , Pré-Escolar , Grânulos Citoplasmáticos/ultraestrutura , Feminino , Histiocitose de Células de Langerhans/patologia , Humanos , Lactente , Recém-Nascido , Células de Langerhans/ultraestrutura , Masculino
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