磁共振成像在评估生长迟缓儿童脑垂体状况中的应用

Elena A. Finota
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Using a high-field magnetic resonance imager, the brain was scanned in the axial, coronal, and sagittal planes using standard modes and targeted examination of the pituitary region using T1- and T2-weighted pulse sequences with a slice thickness of 2.0 mm. Inclusions in the pituitary gland requiring differential diagnosis betwe en adenoma and Rathke’s cleft cyst were imaged with intravenous contrast. The physical development of the children was evaluated using the AntroPlus computer program. The significance of differences between groups was determined by the confidence interval; differences were considered significant at p 0.05. \nRESULTS: Analysis of the obtained data shows that 92.0% of children and adolescents with idiopathic stunting have a standard deviation of growth from –2.0 to –3.0. In these children, hypoplasia of the pituitary gland was found in 36.4% of cases, residual structures of Rathke's cleft cyst in 16.5%, and inactive pituitary adenoma in 4.2%. Normal structure of the pituitary gland was found in the remaining children. In the group of patients with growth hormone deficiency, children with standard deviation of growth coefficient from –3.0 to –4.0 are more frequent (52.6% of patients), and 31.4% of boys and girls have growth retardation more than –4 σ. In these children, in addition to hypothalamic-pituitary masses and hypoplasia of the adenohypophysis, magnetic resonance imaging revealed in 26.7% of cases (including 83.4% of boys and 16.6% of girls) an abnormality of pituitary development in the form of a triad: hypoplasia of the adenohypophysis, shortened pituitary pedicle, and ectopia of the neurohypophysis. In the group of patients with growth retardation due to the presence of hereditary syndromes, 32.7% of those studied had a coefficient of standard deviation of growth between –2.0 and –3.0, and 33.4% had a coefficient of standard deviation of growth between –3.0 and –4.0. 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引用次数: 0

摘要

背景:脑垂体是一种内分泌腺,在调节新陈代谢、身体发育和性发育方面发挥着至关重要的作用。现代医学成像技术可以研究身体发育迟缓儿童下丘脑-垂体区域的变化[1-3]。研究目的:本研究旨在利用磁共振成像技术研究不同形式纳米失调症儿童下丘脑-垂体区域的状况。材料与方法:研究对象包括 102 名男孩和 96 名女孩,他们均主诉生长发育迟缓。研究人员对 8-15 岁儿童和青少年的脑部进行了磁共振成像,并对垂体区域进行了有针对性的研究。使用高场强磁共振成像仪,以标准模式对大脑进行轴向、冠状和矢状面扫描,并使用 T1 和 T2 加权脉冲序列对垂体区域进行有针对性的检查,切片厚度为 2.0 毫米。通过静脉注射造影剂,对需要鉴别诊断垂体腺瘤和拉斯克裂囊肿的垂体内含物进行成像。使用 AntroPlus 计算机程序对儿童的身体发育情况进行评估。组间差异的显著性由置信区间决定;P 0.05 为差异显著。结果:对所得数据的分析表明,92.0%的特发性发育迟缓儿童和青少年的生长标准偏差为-2.0至-3.0。在这些儿童中,36.4%的病例发现垂体发育不良,16.5%的病例发现拉氏裂囊肿残留结构,4.2%的病例发现非活动性垂体腺瘤。其余儿童的垂体结构正常。在生长激素缺乏症患者中,生长系数标准偏差在-3.0至-4.0之间的儿童较多(占患者总数的52.6%),31.4%的男孩和女孩生长迟缓超过-4 σ。在这些患儿中,除了下丘脑-垂体肿块和腺泡发育不全外,磁共振成像还发现26.7%的病例(包括83.4%的男孩和16.6%的女孩)存在垂体发育异常,表现为三联征:腺泡发育不全、垂体蒂缩短和神经骺异位。在因遗传综合征而导致生长迟缓的患者中,32.7%的人的生长标准偏差系数在-2.0 和-3.0 之间,33.4%的人的生长标准偏差系数在-3.0 和-4.0 之间。在生长迟缓较严重的儿童中,磁共振显示空蝶鞍(22.6%)和垂体发育不良(34.8%)的情况更为常见。结论:磁共振成像是评估垂体的主要方法[4]。特发性发育迟缓儿童的生长标准偏差系数是其他组别男孩和女孩的 5.4 倍。在生长激素缺乏症儿童群体中,-3.0 至 -4.0 的标准偏差系数是遗传性综合征儿童的 1.6 倍。在垂体发育不良的儿童中,有三分之一的儿童生长缺陷大于-4 σ,表现为垂体发育异常,即三联征(腺嗜铬细胞发育不全、垂体回变短和神经嗜铬细胞异位)。相比之下,其他组没有发现这种异常。单个病例的生长标准偏差系数大于-4。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Magnetic resonance imaging in assessing the condition of the pituitary gland in children with growth retardation
BACKGROUND: The pituitary gland is an endocrine gland that plays a crucial role in the regulation of metabolism, physical and sexual development. Modern medical imaging techniques allow the study of changes in the hypothalamic-pituitary region in children with low physical development [1–3]. AIM: The aim of the study was to investigate the state of the hypothalamic-pituitary region in children with different forms of nanism using magnetic resonance imaging. MATERIALS AND METHODS: The study included 102 boys and 96 girls with complaints of growth retardation. Magnetic resonance imaging of the brain with targeted studies of the pituitary region of children and adolescents aged 8–15 years was studied. Using a high-field magnetic resonance imager, the brain was scanned in the axial, coronal, and sagittal planes using standard modes and targeted examination of the pituitary region using T1- and T2-weighted pulse sequences with a slice thickness of 2.0 mm. Inclusions in the pituitary gland requiring differential diagnosis betwe en adenoma and Rathke’s cleft cyst were imaged with intravenous contrast. The physical development of the children was evaluated using the AntroPlus computer program. The significance of differences between groups was determined by the confidence interval; differences were considered significant at p 0.05. RESULTS: Analysis of the obtained data shows that 92.0% of children and adolescents with idiopathic stunting have a standard deviation of growth from –2.0 to –3.0. In these children, hypoplasia of the pituitary gland was found in 36.4% of cases, residual structures of Rathke's cleft cyst in 16.5%, and inactive pituitary adenoma in 4.2%. Normal structure of the pituitary gland was found in the remaining children. In the group of patients with growth hormone deficiency, children with standard deviation of growth coefficient from –3.0 to –4.0 are more frequent (52.6% of patients), and 31.4% of boys and girls have growth retardation more than –4 σ. In these children, in addition to hypothalamic-pituitary masses and hypoplasia of the adenohypophysis, magnetic resonance imaging revealed in 26.7% of cases (including 83.4% of boys and 16.6% of girls) an abnormality of pituitary development in the form of a triad: hypoplasia of the adenohypophysis, shortened pituitary pedicle, and ectopia of the neurohypophysis. In the group of patients with growth retardation due to the presence of hereditary syndromes, 32.7% of those studied had a coefficient of standard deviation of growth between –2.0 and –3.0, and 33.4% had a coefficient of standard deviation of growth between –3.0 and –4.0. In children with more severe growth retardation, magnetic resonance signs of empty sella (22.6%) and hypoplasia of the pituitary gland (34.8%) were more frequently visualized. CONCLUSIONS: Magnetic resonance imaging is the primary method for evaluating the pituitary gland [4]. Children with idiopathic stunting exhibit a coefficient of standard deviation of growth that is 5.4 times less frequent than that observed in boys and girls from other groups. In the group of children with growth hormone deficiency, the coefficient of standard deviation from –3.0 to –4.0 is 1.6 times more frequent than in those with hereditary syndromes. One-third of children with pituitary stunting who exhibited a growth deficit greater than –4 σ exhibited a pituitary developmental anomaly in the form of a triad (hypoplasia of the adenohypophysis, shortening of the pituitary gyrus, and ectopia of the neurohypophysis). In contrast, no such anomaly was found in the other groups. The coefficient of standard deviation of growth greater than –4 was found in single cases.
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