Ghidini A, Sirtori M, Romero R, Yarkoni S, Solomon L, Hobbins J C
Department of Obstetrics and Gynecology, Yale University School of Medicine, New Haven, Connecticut.
Am J Perinatol. 1991 Jan;8(1):44-6. doi: 10.1055/s-2007-999339.
A case of congenital pyruvate kinase deficiency manifested at antenatal ultrasound as isolated hepatosplenomegaly is reported and the differential diagnosis is discussed. An aggressive obstetric management and appropriate neonatal care permitted a favorable neonatal outcome.
报告了一例先天性丙酮酸激酶缺乏症病例,产前超声显示为单纯性肝脾肿大,并讨论了鉴别诊断。积极的产科管理和适当的新生儿护理使新生儿获得了良好的结局。