Differentiation between sickle cell anemia and S/β0 thalassemia

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Abstract

Patient: 37-year-old man of half African and half Italian ethnicity. Chief Complaint: Sickle cell crisis (SCC). History of Present Illness: The patient had severe pain in his lower back that radiated to both thighs. He had been admitted twice in the previous 2 weeks at another hospital due to SCC. Each time, he had been discharged with a prescription for oxycodone. His condition did not respond to the pain medicine; his pain remained uncontrollable. Medical History: The patient has had multiple sickle cell crises since childhood and is a former smoker. He denied alcohol consumption or illegal drug use. Physical Examination Findings: The patient had normal vital signs. No splenomegaly was present. Family History: Both parents carry sickle cell thalassemia. Principal Laboratory Findings: Table 1, Table 2, and Image 1.

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Fanestil, V., & Van Siclen, C. (2015). Differentiation between sickle cell anemia and S/β0 thalassemia. Laboratory Medicine, 46(3), e79–e81. https://doi.org/10.1309/LMKW5VWNUK26LKAX

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