Suppr超能文献

[一例急性起病并反复出现共济失调性构音障碍发作的成人型肾上腺脑白质营养不良病例]

[A case of adult type adrenoleukodystrophy with an acute onset and repeated episodes of ataxic dysarthria].

作者信息

Ochi H, Yamashita Y

机构信息

Department of Neurology, Matsuyama Red Cross Hospital.

出版信息

Rinsho Shinkeigaku. 1996 Nov;36(11):1229-33.

PMID:9046854
Abstract

We report a 30-year-old man with adult type adrenoleukodystrophy (ALD) who manifested an acute onset and repeated episodes of ataxic dysarthria. He noticed a moderate dysarthria after a high grade fever in February of 1995; however, two weeks later his symptom disappeared completely. Three months later, he noticed the dysarthria again and he was referred to our hospital for further examination. General physical findings on admission revealed a dark skin color, pigmentation of gingivae and reduced body hair. Neurologically he was normal except for a moderate ataxic dysarthria. Cranial T2-weighted MRI showed multiple high intensity lesions in the subcortical white matter of frontal lobe, bilateral peritrigonal white matter, splenium of the corpus callosum and bilateral cerebellar white matter. Only cerebellar lesions responsible for his symptom were enhanced on MRI after gadolinium administration. Initially we diagnosed him with multiple sclerosis (MS) based upon the clinical course and MRI findings, and then started corticosteroid treatment. His dysarthria was slightly improved after the treatment and bilateral gadolinium-enhanced lesions of cerebellar white matter on MRI disappeared. Multimodality evoked potentials such as short latency somatosensory evoked potentials, brainstem auditory evoked potentials and pattern-reversal visual evoked potentials, disclosed a prolonged central conduction time associated with bilaterally symmetric individual interpeak latencies. These findings, which supported diffuse and bilateral subclinical demyelinating lesions in the central nervous system, were unusual for MS; therefore his plasma very-long-chain fatty acids (VLCFA) were assayed for ALD. Finally, he was diagnosed with adult type ALD because of the high ratio of C26: 0/C22: 0 (0.075; normal 0.033). It is very difficult to clinically distinguish the early stage of adult type ALD especially in patients like this from MS. Therefore it is useful and important to evaluate not only the level of plasma VLCFA, but also to evaluate multimodality evoked potentials.

摘要

我们报告一名30岁患成人型肾上腺脑白质营养不良(ALD)的男性,其表现为急性起病且反复出现共济失调性构音障碍发作。1995年2月,他在高热后出现中度构音障碍;然而,两周后症状完全消失。三个月后,他再次出现构音障碍,并被转诊至我院进一步检查。入院时的全身体格检查发现皮肤颜色较深、牙龈色素沉着和体毛减少。神经系统检查除中度共济失调性构音障碍外均正常。头颅T2加权磁共振成像(MRI)显示额叶皮质下白质、双侧三角区周围白质、胼胝体压部和双侧小脑白质有多个高信号病变。钆剂注射后MRI仅显示导致其症状的小脑病变有强化。最初,根据临床病程和MRI表现,我们将他诊断为多发性硬化(MS),并开始使用皮质类固醇治疗。治疗后他的构音障碍稍有改善,MRI上双侧小脑白质钆剂强化病变消失。短潜伏期体感诱发电位、脑干听觉诱发电位和图形翻转视觉诱发电位等多模式诱发电位显示中枢传导时间延长,伴有双侧对称的各波峰间潜伏期。这些支持中枢神经系统弥漫性和双侧亚临床脱髓鞘病变的发现,在MS中并不常见;因此,检测了他的血浆极长链脂肪酸(VLCFA)以排查ALD。最终,由于C26:0/C22:0比值较高(0.075;正常为0.033),他被诊断为成人型ALD。临床上很难将成人型ALD的早期阶段,尤其是像这样的患者,与MS区分开来。因此,不仅评估血浆VLCFA水平,而且评估多模式诱发电位是有用且重要的。

引用本文的文献

1
Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia.
PLoS One. 2017 May 8;12(5):e0177296. doi: 10.1371/journal.pone.0177296. eCollection 2017.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验