| Autor(en) |
Titel |
Quelle |
Links |
| Watanabe R, Tatsumi K, Hashimoto S, Tamakoshi A, Kuriyama T, Respiratory Failure Research Group of Japan |
Clinico-epidemiological features of pulmonary histiocytosis X. |
Internal medicine (Tokyo, Japan) 2001, 40: 998 |
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| To define the clinico-epidemiological features of pulmonary histiocytosis X in Japan. |
| Willman CL, Busque L, Griffith BB, Favara BE, McClain KL, Duncan MH, Gilliland DG |
Langerhans'-cell histiocytosis (histiocytosis X)--a clonal proliferative disease. |
The New England journal of medicine 1994 Jul 21; 331: 154 |
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| The lesions of Langerhans'-cell histiocytosis (histiocytosis X), a proliferative histiocytic disorder of unknown cause, contain histiocytes similar in phenotype to dendritic Langerhans' cells. The disease ranges in severity from a fatal leukemia-like disorder to an isolated lytic lesion of bone. Intermediate forms of the disease are usually characterized by multiorgan involvement, diabetes insipidus, and a chronic course. |
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