Wit J M, Schuitema-Dijkstra A, van Buul-Offers S, Opmeer F, Van den Brande J L
Department of Paediatrics, University Hospital for Children and Youth het Wilhelmina Kinderziekenhuis, Utrecht, The Netherlands.
Eur J Pediatr. 1988 Aug;147(6):658-61. doi: 10.1007/BF00442487.
In a 5-year-old boy presenting with clumsiness and excessive growth, a large craniopharyngioma was diagnosed. Biochemically, there was a deficiency of growth hormone, a hypothalamic hypothyroidism and hypocorticalism, a thyroxine binding globulin elevation, an abnormal gonadotropin secretion and a mild hyperprolactinaemia. After removal of the tumour growth stopped almost completely. Plasma insulin-like growth factor (IGF)-I was in the lower normal range. Plasma IGF-II decreased after tumour removal. It is speculated that the tumour produced a growth factor causing excessive growth.
一名5岁男孩因动作笨拙和生长过快前来就诊,被诊断为巨大颅咽管瘤。生化检查发现生长激素缺乏、下丘脑性甲状腺功能减退和皮质功能减退、甲状腺素结合球蛋白升高、促性腺激素分泌异常以及轻度高泌乳素血症。肿瘤切除后,生长几乎完全停止。血浆胰岛素样生长因子(IGF)-I处于正常范围下限。肿瘤切除后血浆IGF-II下降。推测肿瘤产生了一种导致过度生长的生长因子。