Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Adicionar filtros








Intervalo de ano
1.
Korean Journal of Dermatology ; : 186-192, 1994.
Artigo em Coreano | WPRIM | ID: wpr-62634

RESUMO

Letterer-Siwe disease is one of Langerhans cell histiocytosis, with Hand-Schuller-Christian disease and eosinophilic granuloma, characterized by proliferation of Langevha is cell. The clinical course of Letterer-Siwe disease is acute fulmunant of casionally fatal, involving skin and many other internal organs, such as the lymph node, liver, spleen, ung and bone. We present 3 cases of Letterer-Siwe disease with characteristic cutaneous findings and revealed Langerhans granules by imrriunohistochemical stain and electronmicrc scopic examination. All patients died in spite of combined chernotherapy.


Assuntos
Humanos , Granuloma Eosinófilo , Histiocitose de Células de Langerhans , Fígado , Linfonodos , Pele , Baço
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA