Yokoro S, Matsuo M, Ohtsuka T, Ohzeki T
Department of Pediatrics, Fuchu Metropolitan Hospital, Tokyo, Japan.
Biol Neonate. 1990;58(2):69-72. doi: 10.1159/000243234.
A neonatal case of hyperthyrotropinemia is described in association with pseudohypoparathyroidism (PHP). This girl was found to have high serum thyrotropin (TSH) on screening, though serum thyroid hormones were within the normal ranges throughout the observation. The patient's TSH remained above the normal limit until 5 years of age, when she suffered from hypocalcemic tetany and was diagnosed as type-1 PHP on the basis of responsiveness to parathyroid hormone. She also had stigmata of Albright's hereditary osteodystrophy. The results demonstrate that elevated TSH, although thyroid hormone concentrations are normal and medication is not indicated, may be one of the earliest diagnostic clues for PHP.
本文描述了一例与假性甲状旁腺功能减退症(PHP)相关的新生儿促甲状腺激素血症病例。该女孩在筛查时发现血清促甲状腺激素(TSH)升高,尽管在整个观察期间血清甲状腺激素水平均在正常范围内。该患者的TSH在5岁之前一直高于正常上限,当时她出现了低钙性手足搐搦,并根据对甲状旁腺激素的反应被诊断为1型PHP。她还具有艾布赖特遗传性骨营养不良的体征。结果表明,尽管甲状腺激素浓度正常且无需药物治疗,但TSH升高可能是PHP最早的诊断线索之一。