Kuroiwa T, Okabe Y, Hasuo K, Yasumori K, Mizushima A, Masuda K
Department of Radiology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
AJNR Am J Neuroradiol. 1991 Jan-Feb;12(1):161-4.
The purpose of this study was to determine whether the MR findings of idiopathic pituitary dwarfism correlated with a clinical history of perinatal abnormalities and abnormal levels of pituitary hormones. MR examinations of 18 patients with pituitary dwarfism were performed; these patients were divided into two groups: those with ectopic posterior lobes (group 1) and those with normal posterior lobes (group 2). Among the seven patients in group 1, MR showed hyperintense signal at the median eminence of the hypothalamus, which was regarded as the ectopic posterior lobe of the pituitary gland. The mean anteroposterior length and height of the pituitary gland in group 1 patients were significantly smaller than those dimensions in the normal control group; the pituitary stalk was not detected in three of seven patients. Six of seven patients were products of breech presentation with perinatal asphyxia. The peak serum growth hormone level was less than 5 ng/ml when assessed by insulin-induced hypoglycemia or the clonidine test. MR findings in the 11 patients with pituitary dwarfism and normal posterior lobes were normal except that the mean size of the pituitary gland was slightly smaller than that of normal controls. The clinical history of these patients was normal except for perinatal asphyxia in one case. Our findings in patients with pituitary dwarfism, with or without an ectopic posterior pituitary lobe suggest that the ectopic lobe, visualized as a bright spot at the median eminence of the hypothalamus, may be common when pituitary dwarfism follows perinatal anoxic/ischemic episodes.
本研究的目的是确定特发性垂体性侏儒症的磁共振成像(MR)表现是否与围产期异常病史及垂体激素水平异常相关。对18例垂体性侏儒症患者进行了MR检查;这些患者被分为两组:异位后叶组(第1组)和后叶正常组(第2组)。在第1组的7例患者中,MR显示下丘脑正中隆起处有高信号,被认为是垂体的异位后叶。第1组患者垂体的平均前后径和高度显著小于正常对照组;7例患者中有3例未检测到垂体柄。7例患者中有6例为臀位产且伴有围产期窒息。通过胰岛素诱导低血糖或可乐定试验评估时,血清生长激素峰值水平低于5 ng/ml。11例垂体性侏儒症且后叶正常的患者,其MR表现除垂体平均大小略小于正常对照组外均正常。这些患者的病史除1例有围产期窒息外均正常。我们对有或无垂体后叶异位的垂体性侏儒症患者的研究结果表明,当垂体性侏儒症继发于围产期缺氧/缺血发作时,在下丘脑正中隆起处表现为亮点的异位后叶可能较为常见。