Idiopathic hypereosinophilic syndrome with disseminated fatal thrombosis: a case report

Emel Gönüllü; Özgür Mehtap; Hakan Keski; Abdullah Hacıhanefioğlu

doi:10.5606/tgkdc.dergisi.2016.12120

Emel Gönüllü¹, Özgür Mehtap², Hakan Keski², Abdullah Hacıhanefioğlu²

¹Eskişehir Devlet Hastanesi, Romatoloji Kliniği, Eskişehir, Türkiye
²Kocaeli Üniversitesi Tıp Fakültesi, Hematoloji Kliniği, Kocaeli, Türkiye

DOI : 10.5606/tgkdc.dergisi.2016.12120

Systemic diseases may be present in the underlying recurrent and disseminated thromboses. One of them is idiopathic hypereosinophilic syndrome. It is a condition which is associated with the presence of eosinophilia without a secondary u nderlying cause a nd a lso with a n evidence of end-organ damage. Affected end organs are most frequently the heart, lungs, the central and peripheral nervous system, and the skin. Hypereosinophilic disorders are associated with the increased counts of eosinophils in the blood and tissues. Correct diagnosis is of utmost importance for effective management of eosinophilia. Herein, we present a 38-year-old male patient with idiopathic hypereosinophilic syndrome who died due to thrombotic complications.

Keywords : Hypereosinophilic syndrome; systemic disease; trombosis

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