Kobayashi A, Kawai S, Utsunomiya T, Obe Y
Arch Dis Child. 1974 Aug;49(8):641-6. doi: 10.1136/adc.49.8.641.
Radiological studies of bone were performed in infants and children with hepatobiliary disease. Rickets was found in 23 out of 39 patients (59%) with surgically unrepaired biliary atresia, in 4 out of 15 (27%) with surgically repaired biliary atresia, in 11 out of 21 (52%) with neonatal hepatitis, and in 2 out of 4 (50%) with intrahepatic cholestasis. Osteoporosis was found in 23 out of 39 (59%) with unrepaired biliary atresia, in 3 out of 15 (20%) with repaired biliary atresia, in 5 out of 21 (24%) with neonatal hepatitis, and in 1 out of 4 (25%) with intrahepatic cholestasis. 2 girls with Byler disease and 1 infant with choledochal cyst showed no radiological evidence of bone disease. In unrepaired biliary atresia comparative studies of biochemical data in the groups with and without bone disease showed the following. Serum calcium levels were reduced in the patients with bone disease compared with those in the group without it. Serum magnesium levels were markedly reduced in the groups with and without bone disease. The product of serum calcium and phosphorus was reduced in the group with osteoporosis compared with that in the group without it. The raised levels of serum alkaline phosphatase were unrelated to the presence or absence of bone disease.
对患有肝胆疾病的婴幼儿进行了骨骼的放射学研究。在39例手术未修复的胆道闭锁患者中,有23例(59%)发现佝偻病;在15例手术修复的胆道闭锁患者中,有4例(27%)发现佝偻病;在21例新生儿肝炎患者中,有11例(52%)发现佝偻病;在4例肝内胆汁淤积患者中,有2例(50%)发现佝偻病。在39例手术未修复的胆道闭锁患者中,有23例(59%)发现骨质疏松;在15例手术修复的胆道闭锁患者中,有3例(20%)发现骨质疏松;在21例新生儿肝炎患者中,有5例(24%)发现骨质疏松;在4例肝内胆汁淤积患者中,有1例(25%)发现骨质疏松。2例患有比勒病的女孩和1例患有胆总管囊肿的婴儿未显示出骨骼疾病的放射学证据。在手术未修复的胆道闭锁中,对有骨骼疾病组和无骨骼疾病组的生化数据进行比较研究,结果如下。与无骨骼疾病组相比,有骨骼疾病的患者血清钙水平降低。有骨骼疾病组和无骨骼疾病组的血清镁水平均显著降低。与无骨质疏松组相比,骨质疏松组的血清钙磷乘积降低。血清碱性磷酸酶水平升高与骨骼疾病的有无无关。