Modern imaging techniques in GH secretory disorders.

G Scotti, F Triulzi, S Pieralli, S Lipari, F Scomazzoni, M Losa
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Abstract

Magnetic resonance images of the pituitary-hypothalamic area in patients with GH secretory disorders, divided into two groups (hypersecretory and hyposecretory), were studied. In the first group there were 42 patients with pituitary adenoma; size, signal characteristics, direction of growth, and type of enhancement were analyzed and compared with similar studies in 40 age and sex matched control patients with non-GH secreting pituitary adenomas. No significant differences were found except for a higher frequency of chiasm involvement and a more pronounced contrast enhancement in the control group. The hyposecretory group was composed of 101 patients with congenital idiopathic growth hormone deficiency (CIGHD). MR revealed morphological abnormalities consisting of hypoplastic anterior pituitary and ectopic posterior pituitary (PPE) in 59 patients, without evidence of a complete pituitary stalk; in 42 patients the posterior pituitary was in normal position and the pituitary stalk visible. The group with PPE showed a greater frequency of multiple pituitary hormone deficiency (51% vs 12%), breech delivery (30% vs 7%) and associated congenital brain anomalies (12% vs 7%). These data suggest that CIGHD could be the result of a congenital midline brain anomaly in a significant proportion of patients.

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生长激素分泌障碍的现代成像技术。
将生长激素分泌紊乱患者分为高分泌组和低分泌组,对其垂体-下丘脑区磁共振成像进行研究。第一组42例垂体腺瘤;我们分析了40例年龄和性别匹配的非gh垂体腺瘤患者的大小、信号特征、生长方向和增强类型,并与类似研究进行了比较。在对照组中,除了交叉累及的频率更高和对比增强更明显外,没有发现显著差异。低分泌组101例先天性特发性生长激素缺乏症(CIGHD)患者。MR显示59例患者垂体前叶发育不全、垂体后叶异位(PPE),未见垂体柄完整;42例患者垂体后叶位置正常,垂体柄可见。PPE组出现多垂体激素缺乏症(51%比12%)、臀位分娩(30%比7%)和相关先天性脑异常(12%比7%)的频率更高。这些数据表明,CIGHD可能是相当一部分患者先天性中线脑异常的结果。
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