Methemoglobinemia in the Setting of G6PD Deficiency and SARS-CoV-2 Infection

被引:0
|
作者
Azizbayeva, Rinata [1 ]
Drennen, Zachary [2 ]
Solanki, Risha [6 ]
Keshava, Vinay E. [3 ]
Bhagavatula, Rama [4 ]
Sareen, Meera [5 ]
Jiwani, Rahim A. [3 ]
Samhouri, Yazan [4 ]
机构
[1] Allegheny Hlth Network, Dept Family Med, Pittsburgh, PA USA
[2] Allegheny Hlth Network, Dept Anesthesiol, Pittsburgh, PA USA
[3] Allegheny Hlth Network Canc Inst, Dept Med Oncol & Hematol, Pittsburgh, PA USA
[4] Allegheny Hlth Network Canc Inst, Div Hematol & Cellular Therapy, Pittsburgh, PA USA
[5] Allegheny Hlth Network, Dept Crit Care Med, Pittsburgh, PA USA
[6] North Allegheny Sr High Sch, 1749 Stevensan Dr, Sewickley, PA 15143 USA
来源
JOURNAL OF COMMUNITY HOSPITAL INTERNAL MEDICINE PERSPECTIVES | 2023年 / 13卷 / 05期
关键词
Methemoglobinemia; COVID-19; G6PD; SICKLE-CELL TRAIT; SPLENIC SYNDROME;
D O I
10.55729/2000-9666.1223
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report a case of a 58 year old African American male patient with Coronavirus Disease-2019 (COVID-19) in the setting of multiple concomitant hematologic disorders, including Glucose-6-phosphate dehydrogenase deficiency (G6PD deficiency) and sickle cell trait. Typically, G6PD deficiency remains clinically silent, and only a minority of patients will show signs of chronic hemolytic anemia. However, all G6PD deficient patients are at risk of non-immune hemolysis after exposure to a variety of infectious pathogens, including COVID-19. Our patient displayed evidence of methemoglobinemia and subsequent tissue anoxia. We review the theories and mechanisms behind the increased risk of complications and severity of illness in the context of COVID-19 and hematologic disorders. These patients may require alternative treatment pathways due to their comorbidities. This case emphasizes the complications that can arise in this setting, and highlights important considerations for patient treatment.
引用
收藏
页码:61 / 64
页数:6
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