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Sickle cell vasoocclusive crisis and acute chest syndrome at term pregnancy.

机译:足月妊娠时镰状细胞血管闭塞性危机和急性胸综合症。

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摘要

Women with sickle cell anemia are surviving longer and may desire pregnancy. Rare, life-threatening complications of sickle cell anemia, such as acute chest syndrome, may occur at the time of delivery. A 22-year-old woman with sickle cell (HbS/beta+ thalassemia) at 35 weeks of gestation presented with shortness of breath and generalized pain. She was diagnosed with vasoocclusive crisis and acute chest syndrome, managed with exchange transfusion and cesarean delivery, and discharged home with her newborn one week later. Prompt recognition of life-threatening complications of sickle cell anemia in a pregnant woman and collaborative medical and obstetric management are essential to optimize maternal and fetal outcome.
机译:镰状细胞性贫血妇女的生存时间更长,可能希望怀孕。分娩时可能发生罕见的威胁生命的镰状细胞性贫血并发症,例如急性胸腔综合症。一名22岁的女性在妊娠35周时患有镰状细胞(HbS /β+地中海贫血),表现为呼吸急促和全身性疼痛。她被诊断出患有血管闭塞性危机和急性胸综合症,进行了交换输血和剖宫产,并于一周后出生。对孕妇镰状细胞性贫血的危及生命的并发症的及时识别以及医疗和产科合作管理对于优化母婴结局至关重要。

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