Unusual case of adult hemophagocytic syndrome

Babak Tamizifar1, Golnaz Samadi2, Maryam Rismankarzadeh3

  • 1Department of Internal Medicine, School of Medicine, Alzahra Hospital, Isfahan, Iran.

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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