Department of Pediatrics, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
Department of Pediatric Endocrinology, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
Front Endocrinol (Lausanne). 2024 Aug 19;15:1385650. doi: 10.3389/fendo.2024.1385650. eCollection 2024.
Fanconi anemia (FA) is a genomic instability disorder associated with congenital abnormalities, including short stature and the presence of central nervous system anomalies, especially in the hypothalamic-pituitary area. Thus, differences in pituitary size could associate with the short stature observed in these patients. Our aim was to evaluate whether central nervous system abnormalities and pituitary gland volume correlate with height and hormone deficiencies in these patients.
In this cross-sectional exploratory study 21 patients diagnosed with FA between 2017 and 2022 in a Spanish Reference Center were investigated. Magnetic resonance imaging (MRI) was performed and pituitary volume calculated and corelated with height and other endocrine parameters.
The percentage of abnormalities in our series was 81%, with a small pituitary (pituitary volume less than 1 SD) being the most frequent, followed by Chiari malformation type 1. The median value of pituitary volume was -1.03 SD (: -1.56, -0.36). Short stature was found in 66.7% [CI95% 43-85.4]. Total volume (mm increases significantly with age and in pubertal stages. There were no differences between volume SD and pubertal stage, or the presence of endocrine deficiencies. No correlations were found between pituitary volume and the presence of short stature. The intraclass correlation index (ICC) average for volume was 0.85 [CI95% 0.61-0.94] indicating a good-to-excellent correlation of measurements.
Central nervous system anomalies are part of the FA phenotype, the most frequent after pituitary hypoplasia being posterior fossa abnormalities, which may have clinical repercussions in the patient. It is therefore necessary to identify those who could be candidates for neurosurgical intervention. The size of the pituitary gland is smaller in these patients, but this does not seem to be related to hormone deficiency and short stature or exposure to a low dose of total body irradiation.
范可尼贫血(FA)是一种基因组不稳定性疾病,与先天性异常有关,包括身材矮小和中枢神经系统异常,特别是在下丘脑-垂体区域。因此,垂体大小的差异可能与这些患者观察到的身材矮小有关。我们的目的是评估中枢神经系统异常和垂体体积是否与这些患者的身高和激素缺乏有关。
在这项西班牙参考中心于 2017 年至 2022 年期间诊断为 FA 的 21 名患者的横断面探索性研究中,进行了磁共振成像(MRI)检查,并计算和相关垂体体积与身高和其他内分泌参数。
在我们的系列中,异常的百分比为 81%,最常见的是小垂体(垂体体积小于 1 个标准差),其次是 Chiari 畸形 1 型。垂体体积的中位数为-1.03 个标准差(-1.56,-0.36)。发现身材矮小的比例为 66.7%[95%可信区间 43-85.4]。总容积(mm)随着年龄和青春期阶段的增加而显著增加。体积标准差和青春期阶段之间没有差异,也没有内分泌缺乏的差异。没有发现垂体体积与身材矮小之间存在相关性。体积的组内相关系数(ICC)平均值为 0.85[95%可信区间 0.61-0.94],表明测量值具有良好到极好的相关性。
中枢神经系统异常是 FA 表型的一部分,在后颅窝异常之后,最常见的是垂体发育不全,这可能对患者有临床影响。因此,有必要识别那些可能成为神经外科干预候选者。这些患者的垂体较小,但这似乎与激素缺乏和身材矮小或全身照射低剂量无关。