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Reliability of magnetic resonance imaging for the detection of hypopituitarism in children with optic nerve hypoplasia

机译:磁共振成像检测视神经发育不良儿童垂体功能低下的可靠性

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Purpose 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. Design Cross-sectional study. Participants One hundred one children with clinical ONH who underwent MRI of the brain and orbits and a detailed pediatric endocrinologic evaluation. Methods 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. Main Outcome Measures Sensitivity and specificity of MRI findings for the detection of hypopituitarism. Results 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%). Conclusions Neurohypophyseal abnormalities on MRI are sensitive and specific indicators of hypopituitarism in children with ONH.
机译:目的鉴别视神经发育不全(ONH)儿童的垂体功能低下至关重要,因为他们有发育迟缓,癫痫发作或死亡的风险。这项研究的目的是确定磁共振成像(MRI)上神经垂体异常的可靠性,以检测ONH儿童的垂体功能低下。设计横断面研究。参加者接受脑部和眼部MRI以及详细的儿科内分泌学评估的110例临床ONH儿童。方法在1.5 Tesla扫描仪上进行磁共振成像研究。成像协议包括矢状T1加权图像,轴向快速液体衰减的反转恢复/ T2加权图像以及脑的弥散加权图像。眼眶成像包括脂肪饱和的轴向和冠状图像以及高分辨率的轴向T2加权图像。两名小儿神经放射科医生对MRI研究进行了审查,包括视神经发育不全,垂体后叶缺失或异位,垂体漏斗状缺失,透明性隔中缺失,移行异常和半球损伤。审查病历以检查临床检查结果和内分泌状况。所有患者均接受了儿科内分泌科医生的临床评估和标准化的血清学检测,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。放射科医生对患者的内分泌状况和眼底镜检查不了解。主要结果指标用于检测垂体功能低下的MRI表现的敏感性和特异性。结果33例儿童出现垂体漏斗,垂体后叶亮点异位,垂体后叶亮点缺失等神经下垂异常。磁共振成像显示28例垂体功能低下患儿中有27例神经垂体异常(敏感性为96%)。内分泌功能正常的73名儿童中有67名发生了正常的神经垂体(特异性为92%)。结论MRI的神经下垂异常是ONH儿童垂体功能低下的敏感和特异性指标。

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