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Hemophagocytic syndrome and acute pancreatitis in acute systemic lupus erythematosus
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نویسنده
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Alblewi Bushra ,Bukhari Iqbal A. ,Hasan Manal ,Alzahani Abdulaziz ,Bukhari Raed ,Bashawri Layla ,Al Shawarby Muhammad
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منبع
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journal of dermatology and dermatologic surgery - 2014 - دوره : 18 - شماره : 1-2 - صفحه:35 -37
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چکیده
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Hemophagocytic syndrome (hps) is characterized by the activation of histiocytes with prominent hemophagocytosis in bone marrow and other reticuloendothelial systems. it has two forms: primary and secondary. the precise pathogenesis of hps is unclear but a dysregulation of macrophage–lymphocyte interactions with subsequent increases in the levels of both t-cell-derived and macrophagederived cytokines has been suggested. cardinal symptoms of hps are prolonged high fever, hepatosplenomegaly, cytopenias, lymphadenopathy and neurological symptoms. in this report, we present a case systemic lupus erythematosus associated with hps and acute pancreatitis.
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کلیدواژه
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Hemophagocytic syndrome; Acute systemic lupus erythematosus; Acute pancreatitis
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آدرس
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University of Dammam and King Fahd Hospital of the University, College of Medicine, Dermatology Department, Saudi Arabia, University of Dammam and King Fahd Hospital of the University, College of Medicine, Department of Dermatology, Saudi Arabia, University of Dammam and King Fahd Hospital of the University, College of Medicine, Internal Medicine Department, Saudi Arabia, University of Dammam and King Fahd Hospital of the University, College of Medicine, Dermatology Department, Saudi Arabia, University of Dammam and King Fahd Hospital of the University, College of Medicine, Internal Medicine Department, Saudi Arabia, University of Dammam and King Fahd Hospital of the University, College of Medicine, Pathology Department, Saudi Arabia, University of Dammam and King Fahd Hospital of the University, College of Medicine, Pathology Department, Saudi Arabia
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Authors
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