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先天性肾上腺皮质增生症与脑磁共振成像异常。

Congenital adrenal hyperplasia and brain magnetic resonance imaging abnormalities.

作者信息

Samia Younes-Mhenni, Mahdi Kamoun, Baha Zantour, Saida Jerbi-Ommezine, Tahar Sfar Mohamed, Habib Sfar Mohamed

机构信息

Department of Endocrinology and Internal medicine, University Hospital of Mahdia, Tunisia.

出版信息

Clin Pediatr Endocrinol. 2010 Oct;19(4):109-13. doi: 10.1297/cpe.19.109. Epub 2010 Dec 29.

DOI:10.1297/cpe.19.109
PMID:23926386
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3687627/
Abstract

A 15-yr-old male patient with congenital adrenal hyperplasia (CAH) was referred to our department with a one year history of gradual worsening of tremors. He was diagnosed with salt-wasting 21-hydroxylase deficiency CAH at 40 d old and was started on hydrocortisone, fludrocortisone and salt. He was found to have hypertension at 8 yr of age. Detailed investigations failed to detect any cause for secondary hypertension. Physical findings on the current hospitalization objectified obesity, blood pressure of 150/80 mmHg, postural and action tremor, left cerebellar syndrome, reflex tetra pyramidal syndrome and mental decline. Brain magnetic resonance imaging (MRI) showed bilateral periventricular white matter hyperintensity that was more pronounced in the posterior regions and associated with cortico-subcortical atrophy and complete agenesis of the corpus callosum. All investigations for leukoencephalopathy were negative. A diagnosis of brain MRI abnormalities related to CAH was made, and the patient received symptomatic treatment of tremors. Our case report provides evidence of an increased frequency of brain MRI abnormalities in CAH. The literature suggests hormonal imbalance and exposure to excess exogenous glucocorticoids as main probable mechanisms. Thus, in clinical practice, CAH should be considered as one of the possible causes of brain white matter involvement associated with or without cerebral atrophy.

摘要

一名15岁先天性肾上腺皮质增生症(CAH)男性患者因震颤逐渐加重1年转诊至我科。他在40日龄时被诊断为失盐型21-羟化酶缺乏症CAH,开始使用氢化可的松、氟氢可的松和补充盐分治疗。他8岁时被发现患有高血压。详细检查未发现继发性高血压的任何病因。此次住院的体格检查发现有肥胖、血压150/80 mmHg、姿势性和动作性震颤、左侧小脑综合征、反射性锥体束征和智力衰退。脑磁共振成像(MRI)显示双侧脑室周围白质高信号,在后部区域更明显,并伴有皮质-皮质下萎缩和胼胝体完全缺如。所有关于白质脑病的检查均为阴性。诊断为与CAH相关的脑MRI异常,患者接受了震颤的对症治疗。我们的病例报告提供了CAH患者脑MRI异常频率增加的证据。文献表明激素失衡和暴露于过量外源性糖皮质激素是主要的可能机制。因此,在临床实践中,CAH应被视为与脑萎缩相关或不相关的脑白质受累的可能原因之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7724/3687627/fe7a53d6da77/cpe-19-109-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7724/3687627/d85681ead703/cpe-19-109-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7724/3687627/47660c251f24/cpe-19-109-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7724/3687627/fe7a53d6da77/cpe-19-109-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7724/3687627/d85681ead703/cpe-19-109-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7724/3687627/47660c251f24/cpe-19-109-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7724/3687627/fe7a53d6da77/cpe-19-109-g003.jpg

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本文引用的文献

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Neurol Sci. 2010 Apr;31(2):125-31. doi: 10.1007/s10072-009-0158-z. Epub 2009 Oct 7.
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Leukoencephalopathy in 21-beta hydroxylase deficiency: report of a family.21-β羟化酶缺乏症中的白质脑病:一家系报告
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Amygdala volume in patients receiving chronic corticosteroid therapy.
经典型先天性肾上腺皮质增生症青少年的脑白质微观结构差异。
J Clin Endocrinol Metab. 2021 Oct 21;106(11):3196-3212. doi: 10.1210/clinem/dgab520.
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Brain white matter abnormality in a newborn infant with congenital adrenal hyperplasia.一名患有先天性肾上腺增生症的新生儿的脑白质异常。
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