1. A Case of Pulmonary Hypertension Associated with Idiopathic Hypereosinophilic Syndrome
- Author
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Miyuki Ito, Hideo Fujita, Yusuke Ugata, Kenichi Sakakura, Hiroshi Wada, Tatsuro Ibe, Tomio Umemoto, and Shin-ichi Momomura
- Subjects
Adult ,Male ,medicine.medical_specialty ,medicine.drug_class ,Hypertension, Pulmonary ,Hypereosinophilia ,030204 cardiovascular system & hematology ,Gastroenterology ,Diagnosis, Differential ,Leukocyte Count ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,medicine.artery ,Hypereosinophilic Syndrome ,Eosinophilic ,medicine ,Humans ,Glucocorticoids ,Antihypertensive Agents ,reproductive and urinary physiology ,Hypereosinophilic syndrome ,business.industry ,General Medicine ,medicine.disease ,Epoprostenol ,Pulmonary hypertension ,Eosinophils ,Treatment Outcome ,Steroid therapy ,030228 respiratory system ,Pulmonary artery ,Corticosteroid ,Idiopathic hypereosinophilic syndrome ,biological phenomena, cell phenomena, and immunity ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,business - Abstract
Hypereosinophilic syndrome (HES) is characterized by multi-organ damage that is associated with tissue hypereosinophilia. A persistently elevated eosinophilic count is also required for the diagnosis of HES. Although HES affects various organs, damage to pulmonary artery is rarely reported. We present a case of a 39-year-old man who was diagnosed with pulmonary hypertension (PH) associated with idiopathic HES. Although the pulmonary arterial hypertension specific drugs including intravenous epoprostenol could not control his PH, corticosteroid was effective for both hypereosinophilia and PH. Our case suggests the importance of steroid therapy as well as specific drugs for pulmonary arterial hypertension in the treatment of PH associated with HES.
- Published
- 2018
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