Hemophagocytic Lymphohistiocytosis in a Patient With Angioimmunoblastic Lymphoma: A Case Report and Review of the Literature

被引:4
作者
Vella, Josefa E. O. [1 ]
El-Daly, Hesham [1 ]
机构
[1] Univ Hosp Coventry & Warwickshire NHS Trust, Coventry, W Midlands, England
关键词
hemophagocytic lymphohistiocytosis; angioimmunoblastic lymphoma; CELL LYMPHOMA;
D O I
10.1177/1066896912444926
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Hemophagocytic lymphohistiocytosis is a rare disorder characterized by a proliferation of phagocytic histiocytes in hematopoietic organs. It is accompanied by systemic manifestations and frequently has an abrupt onset with a fulminant clinical course and high mortality. Awareness of this condition is important since early diagnosis and initiation of treatment is critical for a successful outcome. The authors report a patient with hemophagocytic lymphohistiocytosis associated with angioimmunoblastic lymphoma, describe the clinical and histological features of hemophagocytic lymphohistiocytosis, and review the literature on this condition.
引用
收藏
页码:606 / 609
页数:4
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