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脑腱黄瘤病的磁共振成像表现谱:疾病进展新标志物的重新定义及证据

The spectrum of magnetic resonance findings in cerebrotendinous xanthomatosis: redefinition and evidence of new markers of disease progression.

作者信息

Mignarri Andrea, Dotti Maria Teresa, Federico Antonio, De Stefano Nicola, Battaglini Marco, Grazzini Irene, Galluzzi Paolo, Monti Lucia

机构信息

Unit of Neurology and Neurometabolic Disorders, Department of Medicine, Surgery and Neurosciences, University of Siena, Viale Bracci 2, 53100, Siena, Italy.

Unit of Diagnostic and Therapeutic Neuroradiology, Azienda Ospedaliera Siena, Siena, Italy.

出版信息

J Neurol. 2017 May;264(5):862-874. doi: 10.1007/s00415-017-8440-0. Epub 2017 Mar 21.

Abstract

Cerebrotendinous xanthomatosis (CTX) is a metabolic disease characterized by systemic signs and neurological impairment, which can be prevented if chenodeoxycholic acid (CDCA) treatment is started early. Despite brain MRI represents an essential diagnostic tool, the spectrum of findings is worth to be reappraised, and follow-up data are needed. We performed clinical evaluation and brain MRI in 38 CTX patients. Sixteen of them who were untreated at baseline examination underwent clinical and MRI follow-up after long-term treatment with CDCA. Brain MRI abnormalities included cortical and cerebellar atrophy, and T2W/FLAIR hyperintensity involving subcortical, periventricular, and cerebellar white matter, the brainstem and the dentate nuclei. Regarding the dentate nuclei, we also observed T1W/FLAIR hypointensity consistent with cerebellar vacuolation and T1W/FLAIR/SW hypointense alterations compatibly with calcification in a subgroup of patients. Long-term follow-up showed that clinical and neuroradiological stability or progression were almost invariably associated. In patients with cerebellar vacuolation at baseline, a worsening over time was observed, while subjects lacking vacuoles were clinically and neuroradiologically stable at follow-up. The brains of CTX patients very often show both supratentorial and infratentorial abnormalities at MRI, the latter being related to clinical disability and including a wide spectrum of dentate nuclei alterations. The presence of cerebellar vacuolation may be regarded as a useful biomarker of disease progression and unsatisfactory response to therapy. On the other hand, the absence of dentate nuclei signal alteration should be considered an indicator of better prognosis.

摘要

脑腱黄瘤病(CTX)是一种代谢性疾病,其特征为全身症状和神经功能损害,如果早期开始使用鹅去氧胆酸(CDCA)治疗,这种疾病是可以预防的。尽管脑部磁共振成像(MRI)是一种重要的诊断工具,但仍值得重新评估其检查结果的范围,并且需要随访数据。我们对38例CTX患者进行了临床评估和脑部MRI检查。其中16例在基线检查时未接受治疗,在接受CDCA长期治疗后进行了临床和MRI随访。脑部MRI异常包括皮质和小脑萎缩,以及T2加权/液体衰减反转恢复序列(T2W/FLAIR)高信号,累及皮质下、脑室周围和小脑白质、脑干和齿状核。关于齿状核,我们还在一部分患者中观察到与小脑空洞形成一致的T1加权/液体衰减反转恢复序列(T1W/FLAIR)低信号,以及与钙化相符的T1加权/液体衰减反转恢复序列/磁敏感加权成像(T1W/FLAIR/SW)低信号改变。长期随访表明,临床和神经放射学的稳定性或进展几乎总是相关的。在基线时有小脑空洞形成的患者中,观察到随着时间推移病情恶化;而在没有空洞的患者中,随访时临床和神经放射学表现稳定。CTX患者的脑部在MRI上经常显示幕上和幕下异常,后者与临床残疾相关,包括多种齿状核改变。小脑空洞形成的存在可被视为疾病进展和治疗反应不佳的有用生物标志物。另一方面,齿状核信号无改变应被视为预后较好的指标。

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