An Asian Variant of Intravascular Lymphomatosis: An Updated Review of Malignant Histiocytosis-Like B-Cell Lymphoma

Malignant histiocytosis-like B-cell lymphoma (MH-like BCL) is characterized clinically by hemophagocytic syndrome (HPS), bone marrow involvement at presentation, and an aggressive clinical course. Yet, it remains an ill-defined disease entity. We recently described five cases of MH-like BCL and sugg...

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Veröffentlicht in:	Leukemia & lymphoma 1999, Vol.33 (5-6), p.459-473
Hauptverfasser:	Murase, Takuhei, Nakamura, Shigeo
Format:	Artikel
Sprache:	eng
Schlagworte:	Asia Asian Continental Ancestry Group cytokine hemophagocytic syndrome Histiocytosis, Non-Langerhans-Cell - ethnology Histiocytosis, Non-Langerhans-Cell - etiology Histiocytosis, Non-Langerhans-Cell - pathology Histiocytosis, Non-Langerhans-Cell - physiopathology Humans intravascular lyrnphornatosis Japan Japan - epidemiology Lymphoma, B-Cell - ethnology Lymphoma, B-Cell - pathology Lymphoma, B-Cell - physiopathology Lymphoma, Large B-Cell, Diffuse - ethnology Lymphoma, Large B-Cell, Diffuse - pathology Lymphoma, Large B-Cell, Diffuse - physiopathology parasite
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