Sorkin J A, Davis P C, Meacham L R, Parks J S, Drack A V, Lambert S R
Department of Ophthalmology, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
Am J Ophthalmol. 1996 Nov;122(5):717-23. doi: 10.1016/s0002-9394(14)70492-1.
Magnetic resonance imaging has been used to examine children with optic nerve hypoplasia for pituitary abnormalities who may be at risk for anterior pituitary hormonal deficiencies. We correlated the sellar and optic pathway anatomic findings on magnetic resonance imaging in children with optic nerve hypoplasia with findings from their endocrinologic and ophthalmologic examinations to determine whether magnetic resonance imaging findings predict anterior and posterior pituitary dysfunction.
A retrospective review identified five children with optic nerve hypoplasia and endocrinopathy who also underwent high resolution volumetric magnetic resonance imaging.
All children had severe bilateral optic nerve hypoplasia and anterior pituitary hormone deficiencies. Three children had no recognizable intrasellar or ectopic posterior pituitary bright spot on magnetic resonance imaging; all had clinical evidence of diabetes insipidus. Two patients with a recognizable but ectopic posterior pituitary did not have diabetes insipidus.
Children with optic nerve hypoplasia and no recognizable posterior lobe of the pituitary gland on magnetic resonance imaging are at risk for both anterior and posterior pituitary dysfunction, whereas those with a posterior lobe on magnetic resonance imaging appear to have intact posterior pituitary function.
磁共振成像已被用于检查患有视神经发育不全的儿童是否存在垂体异常,这些儿童可能有垂体前叶激素缺乏的风险。我们将视神经发育不全儿童磁共振成像的蝶鞍和视路解剖学发现与其内分泌和眼科检查结果进行关联,以确定磁共振成像结果是否能预测垂体前叶和后叶功能障碍。
一项回顾性研究确定了五名患有视神经发育不全和内分泌病且接受了高分辨率容积磁共振成像的儿童。
所有儿童均患有严重的双侧视神经发育不全和垂体前叶激素缺乏。三名儿童在磁共振成像上没有可识别的蝶鞍内或异位垂体后叶亮点;所有儿童都有尿崩症的临床证据。两名有可识别但异位垂体后叶的患者没有尿崩症。
磁共振成像上视神经发育不全且垂体后叶不可识别的儿童有垂体前叶和后叶功能障碍的风险,而磁共振成像上有垂体后叶的儿童似乎垂体后叶功能完好。