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Unusual case of adult hemophagocytic syndrome
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نویسنده
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Tamizifar Babak ,Samadi Golnaz ,Rismankarzadeh Maryam
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منبع
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journal of research in medical sciences - 2014 - دوره : 19 - شماره : 2 - صفحه:178 -180
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چکیده
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Hemophagocytic syndrome (hps) is an uncommon manifestation in systemic lupus erythematosus (sle). clinical features of hps include fever, pancytopenia, abnormal liver enzyme, hepatosplenomegaly, lymphadenopathy, and coagulation disorder. hps comprises primary and reactive forms. herein, we describe a case of untreated sle with hps as one of the first manifestations of systemic lupus.
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کلیدواژه
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Autoimmunity ,hemophagocytic syndrome ,hemophagocytosis ,systemic lupus erythematosus
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آدرس
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isfahan university of medical sciences, School of Medicine, Department of Internal Medicine, ایران, isfahan university of medical sciences, Alzahra Hospital, Department of Internal Medicine, ایران, isfahan university of medical sciences, ایران
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Authors
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