Fleischman Amy, Brue Catherine, Poussaint Tina Young, Kieran Mark, Pomeroy Scott L, Goumnerova Liliana, Scott R Michael, Cohen Laurie E
Division of Endocrinology, Children's Hospital Boston, 300 Longwood Ave, Boston, MA 02115, USA.
Pediatrics. 2005 Jun;115(6):e742-8. doi: 10.1542/peds.2004-2237.
Diencephalic syndrome is a rare but potentially lethal cause of failure to thrive in infants and young children. The diencephalic syndrome includes clinical characteristics of severe emaciation, normal linear growth, and normal or precocious intellectual development in association with central nervous system tumors. Our group initially described a series of 9 patients with diencephalic syndrome and found a reduced prevalence of emesis, hyperalertness, or hyperactivity compared with previous reports. Also, the tumors were found to be larger, occur at a younger age, and behave more aggressively than similarly located tumors without diencephalic syndrome. We have been able to extend our follow-up of the original patients, as well as describe 2 additional cases. Because the mechanism of the growth and endocrinologic findings in diencephalic syndrome has not been explained, we report on these patients in light of current research on hypothalamic factors that affect growth and weight. This study emphasizes diencephalic syndrome as a model for additional study of growth hormone resistance and metabolic regulation of adiposity.
间脑综合征是婴幼儿生长发育不良的一种罕见但可能致命的病因。间脑综合征包括严重消瘦、线性生长正常、智力发育正常或早熟等临床特征,并与中枢神经系统肿瘤相关。我们团队最初描述了一系列9例间脑综合征患者,发现与既往报道相比,呕吐、过度警觉或多动的发生率有所降低。此外,与无间脑综合征的类似部位肿瘤相比,这些肿瘤更大,发病年龄更小,且行为更具侵袭性。我们能够延长对原患者的随访时间,并描述另外2例病例。由于间脑综合征生长及内分泌表现的机制尚未得到解释,我们根据当前关于影响生长和体重的下丘脑因素的研究报告这些患者情况。本研究强调间脑综合征可作为进一步研究生长激素抵抗和肥胖代谢调节的模型。