Life-threatening delayed hyperhemolytic transfusion reaction in a patient with sickle cell disease: effective treatment with eculizumab followed by rituximab

Author:

Boonyasampant Mark1,Weitz Ilene C.2,Kay Brian1,Boonchalermvichian Chaiyaporn2,Liebman Howard A.2,Shulman Ira A.1

Affiliation:

1. Department of Pathology; Los Angeles County-University of Southern California Medical Center

2. Jane Anne Nohl Division of Hematology; Department of Medicine; Keck School of Medicine; Los Angeles California

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Cited by 43 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Complement involvement in sickle cell disease;La Presse Médicale;2023-12

2. Complement biology for hematologists;American Journal of Hematology;2023-03-31

3. The Development and Consequences of Red Blood Cell Alloimmunization;Annual Review of Pathology: Mechanisms of Disease;2023-01-24

4. Adverse events of red blood cell transfusions in patients with sickle cell disease;Transfusion and Apheresis Science;2022-10

5. Long-term Use of Eculizumab for Prolonged Hemolysis Following a Delayed Hemolytic Transfusion Reaction in Pediatric Sickle Cell: A Case Report;The Journal of Pediatric Pharmacology and Therapeutics;2022-07-01

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