Differentiation Between Sickle Cell Anemia and S/β⁰ Thalassemia.

Lab Med

Department of Laboratory Medicine and Pathology, Mayo Clinic, Jacksonville, FL.

Published: July 2016

Clinical History 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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Source
http://dx.doi.org/10.1309/LMKW5VWNUK26LKAXDOI Listing

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