Sato T, Saida K, Suzuki Y, Takata I, Ishiguro K
Endocrinol Jpn. 1979 Oct;26(5):623-30. doi: 10.1507/endocrj1954.26.623.
A girl aged 4 years with goiter and accelerated physical and skeletal growth was found to be hyperthyroid on the basis of elevated serum thyroid hormone level, nevertheless both the basal TSH and TSH responsiveness to TRH were maintained within the normal range. Serum TSH was suppressed by exogenous T3 and dexamethasone administration, but not significantly changed after propylthiouracil (PTU) treatment. The diurnal rhythmicity of anterior pituitary hormones was preserved with the high nocturnal peak of TSH and prolactin. Clinically, neither thyrotoxic signs nor evidences of pituitary tumor were observed. Her accelerated growth and elevated thyroid hormone level appeared to be induced by inappropriate secretion of TSH. In view of the literature, this is the first case of the syndrome of inappropriate secretion of TSH excluding the neoplastic origin in Japan.
一名4岁女孩患有甲状腺肿,身体和骨骼生长加速,基于血清甲状腺激素水平升高被发现患有甲状腺功能亢进,但基础促甲状腺激素(TSH)和TSH对促甲状腺激素释放激素(TRH)的反应性均维持在正常范围内。外源性三碘甲状腺原氨酸(T3)和地塞米松给药可抑制血清TSH,但丙硫氧嘧啶(PTU)治疗后无明显变化。垂体前叶激素的昼夜节律得以保留,TSH和催乳素夜间峰值较高。临床上,既未观察到甲状腺毒症体征,也未发现垂体肿瘤的证据。她的生长加速和甲状腺激素水平升高似乎是由TSH分泌不当所致。鉴于文献记载,这是日本首例排除肿瘤起源的不适当TSH分泌综合征病例。