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Three Cases of Letterer - Siwe Disease / 대한피부과학회지
Korean Journal of Dermatology ; : 186-192, 1994.
Article Dans Coréen | WPRIM | ID: wpr-62634
ABSTRACT
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.
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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Peau / Rate / Granulome éosinophile / Histiocytose à cellules de Langerhans / Foie / Noeuds lymphatiques Limites du sujet: Humains langue: Coréen Texte intégral: Korean Journal of Dermatology Année: 1994 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Peau / Rate / Granulome éosinophile / Histiocytose à cellules de Langerhans / Foie / Noeuds lymphatiques Limites du sujet: Humains langue: Coréen Texte intégral: Korean Journal of Dermatology Année: 1994 Type: Article