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布朗-维阿莱托-范莱尔综合征的长期生存:一例强调呼吸护理的病例报告

Long-Term Survival in Brown-Vialetto-Van Laere Syndrome: A Case Report Highlighting Respiratory Care.

作者信息

Lourenço Joana, Moreira Sandra, Leão Miguel, Simão Paula, Ramos Luisa

机构信息

Department of Pulmonology, Pedro Hispano Hospital, Matosinhos Local Health Unit, Matosinhos, PRT.

Department of Neurology, Pedro Hispano Hospital, Matosinhos Local Health Unit, Matosinhos, PRT.

出版信息

Cureus. 2025 May 20;17(5):e84491. doi: 10.7759/cureus.84491. eCollection 2025 May.

Abstract

Brown-Vialetto-Van Laere syndrome (BVVLS) is an extremely rare genetic neurological disorder caused by riboflavin transport deficiency, an autosomal recessive condition mostly associated with mutations in the and genes. It follows a progressive course, typically characterized by sensorineural deafness, facial weakness, ponto-bulbar palsy, ataxia, and peripheral sensory-motor neuropathy. This disease is often associated with childhood mortality if left untreated. We report the case of a 68-year-old woman who first noticed a mild hearing loss at the age of 12. This was followed by a slowly progressive onset of bilateral facial paresis, dysarthro-dysphonia, stridor, and tongue atrophy with fasciculations. At 63 years of age, genetic testing revealed a single heterozygous variant in the gene. Although typically autosomal recessive, some individuals with classic symptoms and even response to riboflavin therapy have been found to carry only a single mutation in either the or gene. Therefore, given the compatible clinical presentation, a diagnosis of BVVLS was considered after discussion with a center of expertise. Consequently, 10 mg/kg/day of riboflavin supplementation was prescribed for three years, but no significant clinical improvement was observed. Currently, at age 68, the patient is on nocturnal non-invasive mechanical ventilation (NIV) and uses assisted airway clearance techniques, including air-stacking maneuvers and mechanical insufflation-exsufflation on demand, due to respiratory compromise secondary to diaphragmatic weakness and vocal cord paralysis. This unique presentation of slowly progressive symptoms and long survival may be related to the single heterozygous variant found. Respiratory care in BVVLS is currently adapted from other neuromuscular disorders with stronger evidence bases. This case highlights the critical role of pulmonology in BVVLS care, including clinical and functional monitoring, early initiation of NIV, and the implementation of airway clearance techniques.

摘要

布朗 - 维阿莱托 - 范莱尔综合征(BVVLS)是一种极其罕见的遗传性神经疾病,由核黄素转运缺陷引起,这是一种常染色体隐性疾病,主要与 和 基因的突变有关。它呈进行性发展,典型特征为感音神经性耳聋、面部无力、脑桥延髓麻痹、共济失调以及周围感觉运动神经病变。如果不进行治疗,这种疾病常与儿童期死亡相关。我们报告一例68岁女性病例,她12岁时首次注意到轻度听力损失。随后逐渐出现双侧面部轻瘫、构音障碍 - 发声困难、喘鸣以及伴有肌束震颤的舌萎缩。63岁时,基因检测发现 基因存在一个杂合变异。尽管该病通常为常染色体隐性遗传,但已发现一些具有典型症状甚至对核黄素治疗有反应的个体在 或 基因中仅携带一个突变。因此,鉴于临床表现相符,在与一个专业中心讨论后考虑诊断为BVVLS。随后,给予每日10mg/kg的核黄素补充剂,持续三年,但未观察到明显的临床改善。目前,68岁的患者因膈肌无力和声门麻痹继发呼吸功能不全,正在接受夜间无创机械通气(NIV),并使用辅助气道清理技术,包括空气堆叠手法和按需机械吸气 - 呼气。这种缓慢进展症状和长期存活的独特表现可能与所发现的单个杂合 变异有关。BVVLS的呼吸护理目前是借鉴其他有更强证据基础的神经肌肉疾病。该病例突出了肺病学在BVVLS护理中的关键作用,包括临床和功能监测、早期启动NIV以及实施气道清理技术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08a9/12178585/c2c1da6fe115/cureus-0017-00000084491-i01.jpg

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