Department of Radiology, Arkansas Children's Hospital, University of Arkansas Medical Center, Little Rock, Arkansas; Department of Ophthalmology, University of Arkansas Medical Center, Arkansas Children's Hospital, Little Rock, Arkansas.
Department of Neuro-Ophthalmology, John A. Moran Eye Center, University of Utah, Salt Lake City, Utah.
Ophthalmology. 2014 Jan;121(1):387-391. doi: 10.1016/j.ophtha.2013.07.001. Epub 2013 Aug 21.
It is essential to identify hypopituitarism in children with optic nerve hypoplasia (ONH) because they are at risk for developmental delay, seizures, or death. The purpose of this study is to determine the reliability of neurohypophyseal abnormalities on magnetic resonance imaging (MRI) for the detection of hypopituitarism in children with ONH.
Cross-sectional study.
One hundred one children with clinical ONH who underwent MRI of the brain and orbits and a detailed pediatric endocrinologic evaluation.
Magnetic resonance imaging studies were performed on 1.5-Tesla scanners. The imaging protocol included sagittal T1-weighted images, axial fast fluid-attenuated inversion-recovery/T2-weighted images, and diffusion-weighted images of the brain. Orbital imaging included fat-saturated axial and coronal images and high-resolution axial T2-weighted images. The MRI studies were reviewed by 2 pediatric neuroradiologists for optic nerve hypoplasia, absent or ectopic posterior pituitary, absent pituitary infundibulum, absent septum pellucidum, migration anomalies, and hemispheric injury. Medical records were reviewed for clinical examination findings and endocrinologic status. All patients underwent a clinical evaluation by a pediatric endocrinologist and a standardized panel of serologic testing that included serum insulin-like growth factor-1, insulin-like growth factor binding protein-3, prolactin, cortisol, adrenocorticotropic hormone, thyroid-stimulating hormone, and free thyroxine levels. Radiologists were masked to patients' endocrinologic status and funduscopic findings.
Sensitivity and specificity of MRI findings for the detection of hypopituitarism.
Neurohypophyseal abnormalities, including absent pituitary infundibulum, ectopic posterior pituitary bright spot, and absent posterior pituitary bright spot, occurred in 33 children. Magnetic resonance imaging disclosed neurohypophyseal abnormalities in 27 of the 28 children with hypopituitarism (sensitivity, 96%). A normal neurohypophysis occurred in 67 of 73 children with normal endocrinologic function (specificity, 92%).
Neurohypophyseal abnormalities on MRI are sensitive and specific indicators of hypopituitarism in children with ONH.
在视神经发育不全(ONH)患儿中识别垂体功能减退症至关重要,因为他们存在发育迟缓、癫痫发作或死亡的风险。本研究的目的是确定磁共振成像(MRI)中神经垂体异常对检测 ONH 患儿垂体功能减退症的可靠性。
横断面研究。
101 名临床诊断为 ONH 的患儿,均接受了脑部和眼眶 MRI 检查以及详细的儿科内分泌评估。
MRI 检查在 1.5T 扫描仪上进行。成像方案包括矢状 T1 加权图像、轴位快速液体衰减反转恢复/T2 加权图像和脑弥散加权图像。眼眶成像包括脂肪饱和轴位和冠状位图像以及高分辨率轴位 T2 加权图像。2 名儿科神经放射科医生对 MRI 研究进行了视神经发育不全、垂体后叶缺如或异位、垂体柄缺如、透明隔缺如、移行异常和半球损伤的评估。对病历进行了回顾,以了解临床检查结果和内分泌状态。所有患者均由儿科内分泌医生进行临床评估,并进行了包括血清胰岛素样生长因子-1、胰岛素样生长因子结合蛋白-3、催乳素、皮质醇、促肾上腺皮质激素、促甲状腺激素和游离甲状腺素水平的标准化检测。放射科医生对患者的内分泌状态和眼底检查结果进行了屏蔽。
MRI 发现对垂体功能减退症检测的敏感性和特异性。
33 名患儿存在神经垂体异常,包括垂体柄缺如、垂体后叶异位亮点和垂体后叶亮点缺如。MRI 显示 28 名垂体功能减退症患儿中有 27 名存在神经垂体异常(敏感性,96%)。67 名内分泌功能正常的患儿中 MRI 显示正常神经垂体(特异性,92%)。
MRI 上的神经垂体异常是 ONH 患儿垂体功能减退症的敏感和特异指标。