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Orthotopic Heart Transplantation in a Child With Hereditary Spherocytosis

机译:遗传性球囊增多症患儿的原位心脏移植

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Hereditary spherocytosis (HS) is a genetic, frequently familial hemolytic blood disease that presents with varying degrees of hemolytic anemia, splenomegaly, and jaundice. The disease arises as a result of defects in any of a number of proteins responsible for maintaining the shape and flexibility of the red blood cell, resulting in an osmotically fragile and characteristically spherical red blood cell. Theoretically, cardiopulmonary bypass can exacerbate hemolysis and subsequent renal dysfunction. There are few reports of open heart surgery for patients with HS and none for orthotopic heart transplantation. We report a 6-year-old boy with HS who underwent orthotopic heart transplantation.
机译:遗传性球血细胞增多症(HS)是一种遗传性家族性溶血性血液病,表现为不同程度的溶血性贫血,脾肿大和黄疸。该疾病是由于负责维持红细胞的形状和柔韧性的多种蛋白质中的任何一种缺陷而导致的,从而导致了渗透性脆弱和典型球形的红细胞。从理论上讲,体外循环可以加剧溶血和随后的肾功能不全。 HS的患者进行开胸手术的报道很少,原位心脏移植也没有报道。我们报告了一名6岁的HS患男孩,他接受了原位心脏移植手术。

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