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肾上腺脑白质营养不良的罕见变异:一例报告

Rare variability in adrenoleukodystrophy: a case report.

作者信息

Chen Yanming, Polara Farhana, Pillai Anjana

机构信息

Department of Medicine, Lincoln Medical Center, 234 East 149th Street, Bronx, New York, 10451, USA.

出版信息

J Med Case Rep. 2018 Jun 28;12(1):182. doi: 10.1186/s13256-018-1722-z.

Abstract

BACKGROUND

X-linked adrenoleukodystrophy is a genetic disorder with diverse clinical phenotypes. Of these phenotypes, the cerebral form usually manifests during early childhood with rapid cognitive and neurological deterioration and is accompanied by extensive white matter involvement. Adrenomyeloneuropathy, however, usually affects young adults and has focal symptoms typical of spinal cord and peripheral nerve involvement.

CASE PRESENTATION

A 35-year-old African American man with a history of alcohol abuse presented with personality changes and lower extremity weakness. Diffuse demyelination was found on the brain image, and a diagnosis of the cerebral form was made based on the clinical features and genetic test.

CONCLUSIONS

We report a rare case of adult-onset cerebral X-linked leukodystrophy with a clinical phenotype of adrenomyeloneuropathy, and the diagnosis was confounded by a history of alcohol abuse.

摘要

背景

X 连锁肾上腺脑白质营养不良是一种具有多种临床表型的遗传性疾病。在这些表型中,脑型通常在幼儿期出现,伴有快速的认知和神经功能恶化,并伴有广泛的白质受累。然而,肾上腺脊髓神经病通常影响年轻人,具有脊髓和周围神经受累的典型局灶性症状。

病例介绍

一名有酗酒史的 35 岁非裔美国男性出现人格改变和下肢无力。脑部影像显示弥漫性脱髓鞘,根据临床特征和基因检测诊断为脑型。

结论

我们报告了一例罕见的成年起病的脑型 X 连锁白质营养不良病例,其临床表型为肾上腺脊髓神经病,且诊断因酗酒史而混淆。

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