An unusual presentation of Idiopathic hypereosinophilic syndrome

J Thromb Thrombolysis. 2020 Aug;50(2):473-476. doi: 10.1007/s11239-020-02127-2.

Abstract

Hypereosinophilic syndrome (HES) is a rare but life-threatening multi-organ disease which can be complicated by stroke, with devastating outcomes. Eosinophils can accumulate in multiple organs, most commonly involving the heart, skin, lungs, spleen, and liver. Neurological end-organ complications in hypereosinophilic syndrome are unusual and have been established to be of three types: brain infarction, encephalopathy and sensory polyneuropathy. We present a case where acute ischaemic stroke and encephalopathy are early manifestations of Idiopathic HES. It is important to consider HES as an aetiology for stroke and a high eosinophil count is an initial diagnostic clue. Early initiation of steroid therapy can potentially prevent disease progression.

Keywords: Idiopathic hypereosinophilic syndrome; Stroke.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Brain Diseases / diagnosis
  • Brain Diseases / etiology*
  • Brain Diseases / physiopathology
  • Female
  • Glucocorticoids / therapeutic use
  • Humans
  • Hypereosinophilic Syndrome / complications*
  • Hypereosinophilic Syndrome / diagnosis
  • Hypereosinophilic Syndrome / drug therapy
  • Ischemic Stroke / diagnosis
  • Ischemic Stroke / etiology*
  • Ischemic Stroke / physiopathology
  • Prednisolone / therapeutic use
  • Recovery of Function
  • Treatment Outcome

Substances

  • Glucocorticoids
  • Prednisolone