Post Blood Transfusion Hypertensive Encephalopathy in a Child with Congenital Hemolytic Anemia: A Case Report

Abstract

Introduction: Children having hemolytic anemias who have received multiple blood transfusions exhibit a rare complication of development of hypertension and seizures following transfusion, which may or may not be associated with intracranial hemorrhage. Case description: A 9-year-old boy presented with history of progressive paleness of body and weakness for the 30 days. There was a history of blood transfusion one week ago and multiple transfusions for one year of age. Examination revealed tachycardia, tachypnea, severe pallor and splenohepatomegaly. Blood work revealed a hemoglobin level of 4.0 grams with peripheral smear fndings suggestive of hemolytic anemia. After blood transfusion, child complained of diffculty in breathing, vomiting and visual loss, followed by convulsions. Blood pressure was 180/110 mmHg. Seizure was controlled with intravenous midazolam and hypertension with furosemide and labetalol. CT brain was normal. As hypertension got under control, child gradually gained consciousness. Conclusion: A less intensive transfusion regimen among such patients along with prompt management of hypertension can prevent this potentially fatal syndrome.

Authors and Affiliations

Dhiman Arshpreet| Junior Resident, Department of Pediatrics, Katihar Medical College, Katihar, Bihar, India, Corresponding e-mail: arshpreet.d1990@gmail.com

Keywords

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  • EP ID EP12495
  • DOI -
  • Views 368
  • Downloads 26

How To Cite

Dhiman Arshpreet (2017). Post Blood Transfusion Hypertensive Encephalopathy in a Child with Congenital Hemolytic Anemia: A Case Report. International Journal of Medical Research & Health Sciences (IJMRHS), 6(11), 102-104. https://europub.co.uk/articles/-A-12495