The Case of Accelerated Linear Growth Despite Growth Hormone and Insulin-like Growth Factor-I Deficiency

Kyeong Ju Lee, J. Hahm, T. Jung, J. Jung, Soo Kyoung Kim, J. Baek, Won Hyun Lee, H. Yoo, S. Chung
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Abstract

Here we describe a male patient who attained normal height despite combined hypopituitarism with an abnormal growth hormone-insulin-like growth factor (IGF)-I axis. When he was an 18-year-old, he presented with a short stature and underdeveloped external genitalia. The patient had not undergone normal pubertal development and he displayed a height below the fifth percentile. Hormonal and radiological studies revealed the findings of severe anterior pituitary hormone deficiency and an atrophic pituitary gland. There had been no recent follow-ups with the patient or medical treatment since that time. In the current presentation, the patient, now 22 years of age, had attained normal height, yet he remained prepubertal and showed manifestations of delayed bone age and combined hypopituitarism. In addition, the patient’s IGF-II levels were increased for his age. (J Korean Endocr Soc 24:206~211, 2009)
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尽管生长激素和胰岛素样生长因子- 1缺乏,但线性生长加速的案例
在这里,我们描述了一位男性患者,他达到了正常的身高,尽管合并垂体功能低下和生长激素-胰岛素样生长因子(IGF)-I轴异常。当他18岁时,他表现出身材矮小,外生殖器发育不全。患者未经历正常的青春期发育,他的身高低于第5个百分位数。激素和放射学研究显示严重的垂体前叶激素缺乏和垂体萎缩。从那时起,没有对患者进行任何后续随访或治疗。在目前的报告中,患者,现在22岁,已达到正常身高,但他仍然处于青春期前,并表现出骨龄延迟和垂体功能减退的表现。此外,患者的IGF-II水平与其年龄相比有所增加。(韩国医师学报24:206~211,2009)
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