Haemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory disorder resulting from
immune dysfunction reflecting either primary immune deficiency or acquired failure of …

Acute myeloid leukemia (AML) is a clinically and genetically heterogeneous disease
accounting for 15–20% of all childhood acute leukemias, while it is responsible for more …

Hemophagocytic lymphohistiocytosis (HLH), also called hemophagocytic syndrome (HS), is
characterized by phagocyte activation caused by uncontrolled hyperinflammation due to …

Phagocytic activity is occasionally observed in the malignant cells of hematopoietic
neoplasms, such as blasts in acute myeloid leukemia (AML). In the vast majority of cases of …

We present two patients with acute myeloblastic leukemia (FAB AML-M7 and AML-M2)
complicated by hemophagocytic lymphohistiocytosis (HLH) and relevant literature review …

目的探讨急性早幼粒细胞白血病(APL) 诱导缓解后合并噬血细胞综合征(HPS)
的诊断及治疗要点. 方法对1 例诊断APL 患者的临床特点进行分析, 并探讨其可能机制 …

Hemophagocytic lymphohistiocytosis (HLH), also called hemophagocytic syndrome, is an
aggressive hyperinflammatory condition characterized by prolonged fever, cytopenias …

Concurrent perturbations in different driver genes have been reported primarily in
lymphoma. In acute myeloid leukemia (AML), cases with concurrent alterations in 2 driver …

To the Editor: I read with great interest the article by Wiseman et al1 regarding
hemophagocytosis by leukemic megakaryoblasts in acute megakaryoblastic leukemia. Their …

The acute myeloid leukemia secondary to polycythemia vera has a poor prognosis and
survival. We present an extremely rare case of polycythemia vera who developed an acute …