unusual case of adult hemophagocytic syndrome

نویسندگان

babak tamizifar

golnaz samadi

maryam rismankarzadeh

چکیده

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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عنوان ژورنال:
journal of research in medical sciences

جلد ۱۹، شماره ۲، صفحات ۰-۰

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