2021
DOI: 10.1111/ijlh.13689
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Blister and bite cells in G6PD deficiency

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Cited by 5 publications
(2 citation statements)
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“…They are a hallmark of hemoglobinopathies such as thalassemia and Hb C, Hb D, and Hb E as well as liver illness (especially obstructive liver disease), post-splenectomy situations, and obstructive liver disease [30]. Bite cells (degmacytes) or blister cells are produced by phagocytes that have retrieved stiff precipitates of hemoglobin that have been denatured (Heinz bodies); these damaged cells may be the first sign of hemolytic anemia induced by oxidant sensitivity, such as a shortage of glucose-6-phosphate dehydrogenase (G6PD) [31].…”
Section: Shape Variabilitymentioning
confidence: 99%
“…They are a hallmark of hemoglobinopathies such as thalassemia and Hb C, Hb D, and Hb E as well as liver illness (especially obstructive liver disease), post-splenectomy situations, and obstructive liver disease [30]. Bite cells (degmacytes) or blister cells are produced by phagocytes that have retrieved stiff precipitates of hemoglobin that have been denatured (Heinz bodies); these damaged cells may be the first sign of hemolytic anemia induced by oxidant sensitivity, such as a shortage of glucose-6-phosphate dehydrogenase (G6PD) [31].…”
Section: Shape Variabilitymentioning
confidence: 99%
“…Therefore, this case emphasizes the importance of a careful review of blood film morphology (typical morphological changes of erythrocytes during acute hemolytic episode) will be helpful to detect this G6PD deficiency disease. 1…”
Section: Author Contributionsmentioning
confidence: 99%