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Korean Journal of Dermatology ; : 186-192, 1994.
Article Dans Coréen | WPRIM | ID: wpr-62634

Résumé

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.


Sujets)
Humains , Granulome éosinophile , Histiocytose à cellules de Langerhans , Foie , Noeuds lymphatiques , Peau , Rate
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