胎儿酒精谱系障碍患者血管白质脑病的观察:一种关联尚不清楚

Julie Gallien , Nadia Bouhamdani , Mahée Côté , Dominique Bouhamdani , M'Hamed Belkhodja , Nicole Leblanc , Ludivine Chamard-Witkowski
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引用次数: 0

摘要

胎儿酒精谱系障碍(FASD)包括由产前酒精暴露(PAE)引起的广泛的身体和神经损伤。虽然FASD的神经学后果已被充分记录,但其与血管性脑白质病(VL)的潜在关联仍未被充分记录和完全了解。本病例报告提出了一个独特的VL病例,记录于一名20岁的女性,在11岁时被诊断为FASD,为这种未被充分认识和潜在的新关联提供了新的见解。患者从婴儿期开始就有一些神经和神经发育方面的问题,这促使他一生中进行了多次脑磁共振成像(MRI)扫描。最近,非典型神经系统检查和合并症导致转介到神经科调查多发性硬化症的可能诊断。神经学评估,包括安排新的核磁共振成像和回顾以前的扫描,证实了提示VL的进行性白质病变的存在。尽管进行了广泛的诊断检查,包括遗传、代谢和自身免疫检测,但没有发现其他病因。患者的临床病史、神经发育特征和确认的PAE提高了VL与FASD相关的可能性,这是最合理的解释。本病例强调了PAE的潜在血管后果,包括血管生成中断、脑灌注不足和血脑屏障通透性增加,这些机制与VL中所见的相似。因此,它强调了在临床环境中认识到这种可能关联的重要性。FASD患者的早期神经影像学可能有助于及时发现亚临床血管病理,指导治疗策略,并有助于减轻长期神经系统风险。记录这些病例对于扩大临床意识和支持未来的研究至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vascular leukoencephalopathy observed in a patient with fetal alcohol spectrum disorder: An association not yet understood
Fetal alcohol spectrum disorder (FASD) encompasses a broad range of physical and neurological impairments resulting from prenatal alcohol exposure (PAE). While the neurological consequences of FASD are well documented, its potential association with vascular leukoencephalopathy (VL) remains poorly documented and incompletely understood. This case report presents a unique case of VL documented in a 20-year-old female diagnosed with FASD at 11 years of age, offering new insights into this underrecognized and potentially emerging association. The patient had several neurological and neurodevelopmental concerns starting in infancy, which prompted a number of brain Magnetic Resonance Imaging (MRI) scans throughout life. More recently, atypical neurological examination and comorbidities led to a referral to the neurology department to investigate a possible diagnosis of multiple sclerosis. Neurological evaluation, which included ordering a new MRI and reviewing previous scans, confirmed the presence of progressive white matter lesions suggestive of VL. Despite an extensive diagnostic workup, including genetic, metabolic, and autoimmune testing, no alternative etiology was identified. The patient’s clinical history, neurodevelopmental profile, and confirmed PAE raised the possibility of VL being associated with FASD as the most plausible explanation. This case highlights the potential vascular consequences of PAE, including disrupted angiogenesis, cerebral hypoperfusion, and increased blood-brain barrier permeability, mechanisms that mirror those seen in VL. As such, it emphasizes the importance of recognizing this possible association in a clinical setting. Early neuroimaging in FASD patients may facilitate timely detection of subclinical vascular pathology, guide treatment strategies, and help mitigate long-term neurological risks. Documenting such cases is crucial to expanding clinical awareness and supporting future research.
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来源期刊
Brain disorders (Amsterdam, Netherlands)
Brain disorders (Amsterdam, Netherlands) Neurology, Clinical Neurology
CiteScore
1.90
自引率
0.00%
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审稿时长
51 days
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