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05 January 2022: Articles

Delayed Hemolytic Transfusion Reaction in Sickle Cell Disease: A Case Series

Unknown etiology, Challenging differential diagnosis, Diagnostic / therapeutic accidents, Unusual setting of medical care, Educational Purpose (only if useful for a systematic review or synthesis)

Abrar J. Alwaheed A , Safi G Alqatari A , Amal Shehab AlSulaiman A* , Reem Shehab AlSulaiman A

DOI: 10.12659/AJCR.934681

Am J Case Rep 2022; 23:e934681

Table 2. Laboratory values – case 2.

BaselineFirst admissionSecond admissionA few months later
PrePost-PrePost
WBC (4–11 k/uL)1.43.64.54.954.7
Hgb g/dl (Male: 13–18 g/dl, Female: 12–16 g/dl)84.29.35.25.89.1
Platelet k/ul (140–450 k/uL)196115182164222156
Reticulocyte count %10.812.5710.47.25.4
Indirect bilirubin mg/dl1.82.91.91.20.91.6
LDH u/l (81–234 U/L)11261553151411161116449
HbS%68607673
WBC – white blood count; Hgb – haemoglobin; LDH – lactate dehydrogenase; HbS% – percentage of hemoglobin S.

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923