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特发性生长激素缺乏所致生长迟缓:24例患者的磁共振成像表现

Growth retardation due to idiopathic growth hormone deficiencies: MR findings in 24 patients.

作者信息

Ochi M, Morikawa M, Yoshimoto M, Kinoshita E, Hayashi K

机构信息

Department of Radiology, Nagasaki University School of Medicine, Japan.

出版信息

Pediatr Radiol. 1992;22(7):477-80. doi: 10.1007/BF02012987.

Abstract

In this study we evaluated the pituitary-hypothalamic abnormalities of "idiopathic growth hormone (GH) deficiency" as demonstrated by MR imaging. Twenty-four patients were examined with a 1.5-T unit using spin echo T-1 weighted images. The patients were divided into two groups according to MR findings: those with ectopic posterior pituitary glands (12 patients), and those with normal posterior pituitary glands (12 patients). Ten patients in the former group and four in the latter group had small anterior pituitary glands. All patients in the former group but only four in the latter group had severe GH deficiencies. Multiple hormone deficiencies were found in eight patients in the former group, but in only two in the latter group. Among the 12 patients with posterior pituitary ectopia, 11 were males, 10 had been born by breech delivery, and four had a history of asphyxia. It is speculated that perinatal abnormalities can cause posterior pituitary ectopia and that there is a close correlation between breech delivery and the male disadvantage of posterior pituitary ectopia. Half of our patients with "idiopathic GH deficiency" had ectopic posterior pituitaries. GH deficiency with posterior pituitary ectopia should no longer be considered idiopathic because organic lesions can now be identified during life.

摘要

在本研究中,我们通过磁共振成像(MR)评估了“特发性生长激素(GH)缺乏症”患者的垂体 - 下丘脑异常情况。使用1.5-T设备,通过自旋回波T1加权成像对24例患者进行了检查。根据MR检查结果,将患者分为两组:垂体后叶异位组(12例患者)和垂体后叶正常组(12例患者)。前一组中有10例患者垂体前叶较小,后一组中有4例患者垂体前叶较小。前一组的所有患者均存在严重的GH缺乏症,而后一组中只有4例患者存在严重的GH缺乏症。前一组中有8例患者存在多种激素缺乏,而后一组中只有2例患者存在多种激素缺乏。在12例垂体后叶异位的患者中,11例为男性,10例为臀位分娩,4例有窒息史。推测围产期异常可导致垂体后叶异位,且臀位分娩与垂体后叶异位的男性易患倾向之间存在密切关联。我们的“特发性GH缺乏症”患者中有一半存在垂体后叶异位。伴有垂体后叶异位的GH缺乏症不应再被视为特发性,因为现在可以在患者生前识别出器质性病变。

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