Hyperhemolytic Crisis Following Transfusion in Sickle Cell Disease With Acute Hepatic Crisis: A Case Report

Hyperhemolysis syndrome (HHS) is a catastrophic unpredictable consequence of blood transfusion in sickle cell disease. It leads to further drop in hemoglobin via immune mechanisms complicating a hospital course and prolonging length of stay. Although sickle cell patients receive multiple transfusion...

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Detalles Bibliográficos
Autores principales: Trivedi, Krunal, Abbas, Ahmed, Kazmi, Riyashat, Shaaban, Hamid, Miller, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Allergy/Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9461243/
https://www.ncbi.nlm.nih.gov/pubmed/36110470
http://dx.doi.org/10.7759/cureus.27844

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9461243/
https://www.ncbi.nlm.nih.gov/pubmed/36110470
http://dx.doi.org/10.7759/cureus.27844

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