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磁共振成像检测X连锁肾上腺脑白质营养不良成年患者的病变进展

Magnetic resonance imaging detection of lesion progression in adult patients with X-linked adrenoleukodystrophy.

作者信息

Eichler Florian, Mahmood Asif, Loes Daniel, Bezman Lena, Lin Doris, Moser Hugo W, Raymond Gerald V

机构信息

Department of Neurology, Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Arch Neurol. 2007 May;64(5):659-64. doi: 10.1001/archneur.64.5.659.

Abstract

BACKGROUND

An inherited disorder, X-linked adrenoleukodystrophy (X-ALD) is known to cause progressive inflammatory demyelination.

OBJECTIVE

To analyze the adult pattern of disease progression in X-ALD.

DESIGN, SETTING, AND PATIENTS: We retrospectively assessed magnetic resonance (MR) images obtained in adult patients who had developed cerebral disease between January 1, 1985, and December 31, 2005. We identified 103 adult patients with X-ALD with lesions on their MR images. Of these, 56 had serial MR examinations at least 1 year apart and were included in this study. Main Outcome Measure Progression of X-ALD lesions on MR images.

RESULTS

On initial presentation, 17 patients with X-ALD had corticospinal tract lesions without splenium or genu involvement, 24 had symmetric corticospinal tract lesions with additional involvement of the splenium or genu, and 15 did not have corticospinal tract involvement but had other white matter lesions. In 18 of 21 patients with progressive lesions, corticospinal tract involvement preceded or occurred concurrently with progressive inflammatory demyelination.

CONCLUSIONS

Brain MR imaging abnormalities in adults with X-ALD progress slower than those reported in childhood. The involvement of the corticospinal tracts is prominent and may at times represent a variant course of progressive inflammatory demyelination.

摘要

背景

X连锁肾上腺脑白质营养不良(X-ALD)是一种遗传性疾病,已知可导致进行性炎症性脱髓鞘。

目的

分析X-ALD的成人疾病进展模式。

设计、地点和患者:我们回顾性评估了1985年1月1日至2005年12月31日期间患有脑部疾病的成年患者的磁共振(MR)图像。我们确定了103例MR图像上有病变的成年X-ALD患者。其中,56例患者进行了间隔至少1年的系列MR检查,并纳入本研究。主要观察指标为MR图像上X-ALD病变的进展情况。

结果

初次就诊时,17例X-ALD患者有皮质脊髓束病变,不累及压部或膝部;24例有对称性皮质脊髓束病变,同时累及压部或膝部;15例无皮质脊髓束受累,但有其他白质病变。在21例有进展性病变的患者中,18例皮质脊髓束受累先于或与进行性炎症性脱髓鞘同时发生。

结论

成人X-ALD患者的脑MR成像异常进展比儿童期报道的要慢。皮质脊髓束受累较为突出,有时可能代表进行性炎症性脱髓鞘的一种变异病程。

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