Affiliations 

  • 1 Department of Paediatrics, School of Medicine and Health Sciences, Monash University, Johor Bahru, 80100 Johor, Malaysia ngim.chin.fang@monash.edu
  • 2 Department of Nuclear Medicine, Sultanah Aminah Hospital, Johor Bahru, 80100 Johor, Malaysia
  • 3 Paediatrics and Child Health Research Group, Department of Paediatrics, University of Malaya Medical Centre, 50603 Kuala Lumpur, Malaysia
J Trop Pediatr, 2014 Jun;60(3):253-6.
PMID: 24473404 DOI: 10.1093/tropej/fmu003

Abstract

A rare syndrome of hypertension, seizures and intracranial bleed has been reported among patients with congenital hemolytic anemia who underwent multiple blood transfusions. We report this syndrome in a 12-year-old Malay girl with hemoglobin E-beta-thalassemia, who underwent intensive transfusion and subsequently had headache, visual loss, severe hypertension and seizures. A comprehensive literature review revealed 30 patients with this syndrome, of whom 15 had intracranial bleed and 12 among these 15 died. A less-intensive transfusion regimen among patients with chronic hemolytic anemia and prompt detection and management of hypertension may prevent this potentially fatal syndrome.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.