Abstract
A 31-year-old pregnant woman at 20 weeks' gestation was sent to our hospital for fever, anemia, and arthralgias. As she was known to be a double heterozygote for beta-thalassemia and hemoglobin S, a diagnosis of hemolytic anemia caused by sickled red cells vasocclusive crises was made. The patient was submitted to partial exchange transfusion (PET) with a complete recovery. A second PET was performed at 36 weeks' gestation, and elective cesarean section was performed at 37 weeks, with the birth of a normal female neonate.
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Anemia, Sickle Cell / complications
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Anemia, Sickle Cell / diagnosis*
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Anemia, Sickle Cell / genetics
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Bilirubin / blood
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Biomarkers / blood
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Exchange Transfusion, Whole Blood / standards
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Female
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Hemoglobin, Sickle / genetics
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Hemoglobins / analysis
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Heterozygote
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Humans
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L-Lactate Dehydrogenase / blood
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Pregnancy
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Pregnancy Complications, Hematologic / diagnosis*
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Pregnancy Complications, Hematologic / therapy
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Pregnancy Outcome
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beta-Thalassemia / complications
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beta-Thalassemia / diagnosis*
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beta-Thalassemia / genetics
Substances
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Biomarkers
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Hemoglobin, Sickle
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Hemoglobins
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L-Lactate Dehydrogenase
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Bilirubin