Literature DB >> 24473404

Post-transfusion hypertension and seizure in congenital hemolytic anemia: a case report and literature review.

Chin Fang Ngim1, Chen Siew Ng2, Nai Ming Lai3.   

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.
© The Author [2014]. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  hemolytic anemia; hypertension; intracranial bleed; seizures; transfusion

Mesh:

Year:  2014        PMID: 24473404     DOI: 10.1093/tropej/fmu003

Source DB:  PubMed          Journal:  J Trop Pediatr        ISSN: 0142-6338            Impact factor:   1.165


  1 in total

1.  Beta-thalassemia major complicated by intracranial hemorrhage and critical illness polyneuropathy.

Authors:  S Sanju; M S Tullu; S Karande; M N Muranjan; P Parekh
Journal:  J Postgrad Med       Date:  2019 Jul-Sep       Impact factor: 1.476

  1 in total

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