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Reactive hemophagocytic syndrome as a presenting feature of Hodgkin's disease
Authors:L. Dawson  G. J. den Ottolander  P. M. Kluin  O. Leeksma
Affiliation:(1) Department of Internal Medicine, Leiden University, Medical Centre, C1-R41, P.O. Box 9600, 2300 RC Leiden, The Netherlands, NL;(2) Department of Hematology, Leiden University, Medical Centre, The Netherlands, NL;(3) Department of Pathology, Leiden University, Medical Centre, The Netherlands, NL
Abstract:We report the case of a 60-year-old man with febris of unknown origin, severe pancytopenia, and rapidly developing splenomegaly due to reactive hemophagocytic syndrome and Hodgkin's disease. Reactive hemophagocytic syndrome is often rapidly fatal and, once this diagnosis is considered, an underlying infection or malignancy should be treated promptly. An extensive search of the literature revealed only two other cases of reactive hemophagocytic syndrome and Hodgkin's disease. This is the only reported patient who survived after being diagnosed as having reactive hemophagocytic syndrome and Hodgkin's disease. Received: 12 October 1998 / Accepted: 4 November 1999
Keywords:Hodgkin's disease  Reactive hemophagocytic syndrome  Pancytopenia  Ferritin
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