Yakabe S, Ikeda K, Ohgami H, Nakagawara A, Matsuo S, Yae Y
Z Kinderchir. 1984 Jun;39(3):168-70. doi: 10.1055/s-2008-1044203.
Quantitative lipoprotein-X (Lp-X) was measured for diagnostic and postoperative examination of congenital biliary atresia (CBA). There was no significant difference in the levels in children with CBA (n = 23) or neonatal hepatitis (NH) (n = 14). However, a value over 200 mg/dl was found in 7 of CBA but not NH patients. As to 13 postoperative non-icteric patients with CBA, Lp-X was absent in only 2 patients. Thus, postoperative patients without jaundice do not always have a normal biliary secretion. From those results, estimation of Lp-X is both useful for diagnosis and postoperative evaluation of CBA.
对先天性胆道闭锁(CBA)进行诊断及术后检查时测定了定量脂蛋白-X(Lp-X)。CBA患儿(n = 23)和新生儿肝炎(NH)患儿(n = 14)的Lp-X水平无显著差异。然而,7例CBA患儿Lp-X值超过200mg/dl,而NH患儿未出现此情况。对于13例术后无黄疸的CBA患儿,仅2例未检测到Lp-X。因此,术后无黄疸的患儿胆汁分泌并非总是正常。基于这些结果,Lp-X的测定对CBA的诊断及术后评估均有用。