Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova, Genova, Italy.
Department of Pediatrics, IRCCS Istituto Giannina Gaslini, Genova, Italy.
J Clin Endocrinol Metab. 2020 Nov 1;105(11). doi: 10.1210/clinem/dgaa540.
The etiology of central diabetes insipidus (CDI) in children is often unknown. Clinical and radiological features at disease onset do not allow discrimination between idiopathic forms and other conditions or to predict anterior pituitary dysfunction.
To evaluate the evolution of pituitary stalk (PS) thickening and the pattern of contrast-enhancement in relation with etiological diagnosis and pituitary function.
We enrolled 39 children with CDI, 29 idiopathic and 10 with Langerhans cell histiocytosis (LCH). Brain magnetic resonance images taken at admission and during follow-up (332 studies) were examined, focusing on PS thickness, contrast-enhancement pattern, and pituitary gland size; T2-DRIVE and postcontrast T1-weighted images were analyzed.
Seventeen of 29 patients (58.6%) with idiopathic CDI displayed "mismatch pattern," consisting in a discrepancy between PS thickness in T2-DRIVE and postcontrast T1-weighted images; neuroimaging findings became stable after its appearance, while "mismatch" appeared in LCH patients after chemotherapy. Patients with larger PS displayed mismatch more frequently (P = 0.003); in these patients, reduction of proximal and middle PS size was documented over time (P = 0.045 and P = 0.006). The pituitary gland was smaller in patients with mismatch (P < 0.0001). Patients with mismatch presented more frequently with at least one pituitary hormone defect, more often growth hormone deficiency (P = 0.033).
The PS mismatch pattern characterizes patients with CDI, reduced pituitary gland size, and anterior pituitary dysfunction. The association of mismatch pattern with specific underlying conditions needs further investigation. As patients with mismatch show stabilization of PS size, we assume a prognostic role of this peculiar pattern, which could be used to lead follow-up.
儿童中枢性尿崩症(CDI)的病因通常不明确。疾病发作时的临床和影像学特征无法区分特发性和其他疾病,也无法预测垂体前叶功能障碍。
评估垂体柄(PS)增厚的演变及其与病因诊断和垂体功能的对比增强模式。
我们纳入了 39 例 CDI 患儿,其中 29 例为特发性,10 例为朗格汉斯细胞组织细胞增生症(LCH)。对入院时和随访期间(332 次研究)的脑磁共振图像进行了检查,重点关注 PS 厚度、对比增强模式和垂体大小;分析 T2-DRIVE 和对比后 T1 加权图像。
29 例特发性 CDI 患儿中 17 例(58.6%)表现出“不匹配模式”,即 T2-DRIVE 中 PS 厚度与对比后 T1 加权图像之间存在差异;该影像学表现出现后趋于稳定,而 LCH 患儿在化疗后出现“不匹配”。PS 较大的患者更常出现不匹配(P = 0.003);这些患者的 PS 近端和中段大小随时间逐渐减小(P = 0.045 和 P = 0.006)。不匹配患者的垂体较小(P < 0.0001)。不匹配患者更常出现至少一种垂体激素缺陷,更常见的是生长激素缺乏(P = 0.033)。
PS 不匹配模式是 CDI、垂体体积减小和垂体前叶功能障碍患者的特征。不匹配模式与特定潜在疾病的关联需要进一步研究。由于不匹配患者的 PS 大小稳定,我们假设这种特殊模式具有预后作用,可用于指导随访。