Postoperative acute multiple organ failure after hepatectomy in a Nigerian male with sickle cell trait: a case report

BACKGROUND: Sickle cell disease (SCD) is a monogenic disease characterized by sickle hemoglobin (HbS). Patients homozygous for HbS experience symptoms resulting from sickled erythrocytes no later than adolescence. However, heterozygous HbS carriers, or those with the so-called sickle cell trait (SCT...

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Dades bibliogràfiques
Publicat a:Surg Case Rep
Autors principals: Iwasaki, Toshimitsu, Nara, Satoshi, Nishimura, Yuuki, Ueda, Hiroki, Kishi, Yoji, Esaki, Minoru, Shimada, Kazuaki, Hiraoka, Nobuyoshi
Format: Artigo
Idioma:Inglês
Publicat: Springer Berlin Heidelberg 2021
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7803851/
https://ncbi.nlm.nih.gov/pubmed/33438090
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40792-020-01102-6
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