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27 April 2026 : Case report  Bahrain

Management of Bilateral Humeral Head Avascular Necrosis in Sickle Cell Disease Using Surgical Intervention With Adjuvant Hyperbaric Oxygen Therapy: A Case Report

Challenging differential diagnosis, Unusual or unexpected effect of treatment, Diagnostic / therapeutic accidents, Unexpected drug reaction, Clinical situation which can not be reproduced for ethical reasons, Rare coexistence of disease or pathology

Abdulla A. Aljowder ACG 1, Waleed Y. Ebrahim E 1, Omar Abusedera ABDEF 2*, Konouz Alfadhli ABCDEFG 2, Noor Jaragh ACDE 2, Leen Zghaier EF 2, Awrad J. Alkhaldi BEF 2

DOI: 10.12659/AJCR.951902

Am J Case Rep 2026; 27:e951902

Table 1 Baseline laboratory findings of the patient.

ParameterPatient valueNormal rangeNote
Hb8.6 g/dL13.5–17.5 g/dL (male) 12–16 g/dL (female)Low, consistent with chronic SCD anemia
Hct26%41–53% (male) 36–46% (female)Low
Reticulocyte count6.8%0.5–2.5%Elevated, indicates compensatory erythropoiesis
WBC9.8×10/L4–11×10/LWithin expected range
Platelet count410×10/L150–450×10/LWithin expected range
ESR18 mm/hr0–20 mm/hNormal
CRP4 mg/L<10 mg/LNormal
HbS fraction78%<5% (normal adults)High, consistent with homozygous SCD
Hb – hemoglobin; Hct – hematocrit; Retic – reticulocyte count; WBC – white blood cell count; Plt – platelet count; ESR – erythrocyte sedimentation rate; CRP – C-reactive protein; HbS – hemoglobin S. Normal ranges are provided for reference.

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