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.
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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