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Monia Ouederni | Zendy; MONIA BEN KHALED | Zendy; Samia Rekaya | Zendy; Ilhem Ben Fraj | Zendy; Fethi Mellouli | Zendy; Mohamed Béjaoui | Zendy

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Author(s) -

Monia Ouederni,

MONIA BEN KHALED,

Samia Rekaya,

Ilhem Ben Fraj,

Fethi Mellouli,

Mohamed Béjaoui

Publication year - 2017

Publication title -

mediterranean journal of hematology and infectious diseases

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.682

H-Index - 31

ISSN - 2035-3006

DOI - 10.4084/mjhid.2017.57

Subject(s) - medicine , family medicine

Hemophagocytic lymphohistiocytosis is a life-threatening hyperinflammation caused by uncontrolled proliferation of activated lymphocytes and histiocytes. Often, Hemophagocytic lymphohistiocytosis is an acquired syndrome. We report a case of a 9 month-old-boy presented with hepatosplenomegaly, severe anemia requiring repeated transfusions, thrombocytopenia, hypertriglyceridemia and very high hyperferritinemia. These clinical features of Hemophagocytic lymphohistiocytosis prompted a wide infectious and auto-immune request to be performed. After a wide diagnostic workup, he was referred to the immune hematologic unit, for hemophagocytic lymphohistiocytosis suspicion with unknown cause

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