Woodhouse N J, Fisher M T, Sigurdsson G, Joplin G F, MacIntyre I
Br Med J. 1972 Nov 4;4(5835):267-9. doi: 10.1136/bmj.4.5835.267.
A five-year-old boy presented with a three-and-a-half-year history of repeated bone fractures and progressive bone deformity. The excretion of hydroxyproline in the urine was greatly increased, and serum alkaline phosphatase and acid phosphatase levels were very high. These abnormalities together with the findings on bone histology and radiology suggested a diagnosis of juvenile Paget's disease. Human calcitonin reduced the bone turnover as evidenced by an immediate and sustained fall in urine hydroxyproline excretion, while calcium and phosphate balance became more positive. This treatment is therefore being continued on an outpatient basis.
一名五岁男孩有三年半反复骨折和进行性骨骼畸形的病史。尿中羟脯氨酸排泄量大幅增加,血清碱性磷酸酶和酸性磷酸酶水平非常高。这些异常情况连同骨组织学和放射学检查结果提示诊断为青少年佩吉特病。人降钙素降低了骨转换,尿羟脯氨酸排泄量立即且持续下降证明了这一点,同时钙和磷平衡变得更加正向。因此,这种治疗正在门诊持续进行。