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A Rare Case of Acute Hemolysis After Rasburicase Infusion
Jacqueline B Broadway-Duren1, Taylor P Gardiner1
1From The University of Texas MD Anderson Cancer Center, Houston, Texas.
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic disorder impacting red blood cells, potentially causing hemolytic anemia. Certain medications can trigger severe reactions in affected individuals.
Area of Science:
- Genetics
- Hematology
- Biochemistry
Background:
- Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked genetic disorder affecting red blood cells.
- It can lead to hemolytic anemia (HA) due to erythrocyte vulnerability to oxidative stress.
- Prevalence is notable in males, affecting approximately 1 in 10 Black males in the US.
Purpose of the Study:
- To summarize a case of hemolytic anemia following rasburicase infusion in a patient with G6PD deficiency.
- To discuss management strategies for such cases.
Main Methods:
- Review of a clinical case involving rasburicase administration.
- Diagnostic tests for hemolytic anemia including Coombs test, haptoglobin, CBC, urinalysis, LDH, bone marrow tests, and peripheral blood smear.
Main Results:
- The patient developed hemolytic anemia after rasburicase infusion.
- Identified specific medications that can trigger hemolytic crisis in G6PD deficient individuals.
Conclusions:
- Rasburicase can precipitate hemolytic crisis in patients with G6PD deficiency.
- Prompt diagnosis and appropriate management are crucial for patients with G6PD deficiency experiencing hemolytic events.
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