Kaga Akimune, Saito-Hakoda Akiko, Uematsu Mitsugu, Kamimura Miki, Kanno Junko, Kure Shigeo, Fujiwara Ikuma
Department of Pediatrics, Tohoku University Hospital, Sendai, Japan.
Clin Pediatr Endocrinol. 2013 Oct;22(4):77-81. doi: 10.1292/cpe.22.77. Epub 2013 Oct 26.
Several studies have described brain white matter abnormalities on magnetic resonance imaging (MRI) in children and adults with congenital adrenal hyperplasia (CAH), while the brain MRI findings of newborn infants with CAH have not been clarified. We report a newborn boy with CAH who presented brain white matter abnormality on MRI. He was diagnosed as having salt-wasting CAH with a high 17-OHP level at neonatal screening and was initially treated with hydrocortisone at 8 days of age. On day 11 after birth, he had a generalized tonic seizure. No evidence of serum electrolyte abnormalities was observed. Brain MRI revealed white matter abnormalities that consisted of bilateral small diffuse hyperintensities on T1-weighted images with slightly low intensity on T2-weighted images in the watershed area. Several factors associated with brain white matter abnormalities in adults with CAH, such as increasing age, hypertension, diabetes and corticosteroid replacement, were not applicable. Although the cause of the phenomenon in this case is unclear, brain white matter abnormality could be observed in newborn infants with CAH as well as in adult patients.
多项研究描述了先天性肾上腺皮质增生症(CAH)患儿及成人在磁共振成像(MRI)上的脑白质异常情况,而CAH新生儿的脑MRI表现尚未明确。我们报告了一名患有CAH的新生儿男孩,其MRI显示脑白质异常。他在新生儿筛查时被诊断为失盐型CAH,17-OHP水平升高,出生8天时开始接受氢化可的松治疗。出生后第11天,他出现全身性强直发作。未观察到血清电解质异常的证据。脑MRI显示白质异常,表现为分水岭区T1加权像上双侧小片状弥漫性高信号,T2加权像上信号略低。CAH成年患者脑白质异常的一些相关因素,如年龄增长、高血压、糖尿病和皮质类固醇替代治疗等,在此病例中并不适用。虽然该病例中这种现象的原因尚不清楚,但在CAH新生儿以及成年患者中均可观察到脑白质异常。