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J Pediatr Hematol Oncol ; 44(5): e881-e883, 2022 07 01.
Article in English | MEDLINE | ID: mdl-35383694

ABSTRACT

Hypereosinophilic syndrome (HES) is a very rare disease during childhood. It involves the different organs like skin, gastrointestinal system, heart and lungs, besides pulmonary hypertension (PHT) is a very rare morbidity of HES that may cause life-threatening complications. PHT improves with the treatment of hypereosinophilia, without the need for pulmonary vasodilator therapy. Here, we present a case of PHT developed after recovery of pulmonary infiltration in an infant with idiopathic HES. We revealed that pulmonary pressure returned to normal range in parallel with the decrease in eosinophil count with steroid treatment.


Subject(s)
Hypereosinophilic Syndrome , Hypertension, Pulmonary , Heart , Humans , Hypereosinophilic Syndrome/complications , Hypereosinophilic Syndrome/drug therapy , Hypertension, Pulmonary/complications , Hypertension, Pulmonary/etiology , Infant , Leukocyte Count , Lung
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