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资源受限环境下脊髓小脑共济失调的临床诊断与管理:来自尼泊尔东部的病例报告

Clinical diagnosis and management of spinocerebellar ataxia in a resource-constrained setting: a case report from Eastern Nepal.

作者信息

Adhikari Nabin, Pokhrel Popular, Kc Priyanka, Kumar Sah Navin, Shah Bhupendra

机构信息

B.P. Koirala Institute of Health Sciences, Dharan, Nepal.

Department of Internal Medicine, B.P. Koirala Institute of Health Sciences, Dharan, Nepal.

出版信息

Ann Med Surg (Lond). 2024 Oct 16;86(12):7385-7389. doi: 10.1097/MS9.0000000000002654. eCollection 2024 Dec.

Abstract

INTRODUCTION

Spinocerebellar ataxias (SCA) are a diverse group of neurodegenerative disorders with autosomal dominant inheritance, primarily affecting the cerebellum and its connections. Diagnosis typically involves genetic testing, but in resource-limited settings, clinical and neuroimaging assessments become critical. This case report highlights the role of nongenetic methods in diagnosing SCA and outlines management strategies in such settings.

CASE PRESENTATION

A 41-year-old male presented with a 2-year history of progressive gait imbalance, headache, and abnormal speech. He had a family history of similar symptoms in two siblings, but no significant past medical history. Clinical examination revealed scanning speech, dysmetria, and a broad-based gait. Clinical and neuroimaging findings, including cerebellar atrophy, led to a diagnosis of SCA in the absence of genetic testing. Patient management with speech, occupational, and physical therapies, showed gradual improvement.

DISCUSSION

SCA, characterized by cerebellar atrophy and a range of clinical symptoms, is typically diagnosed through genetic testing, but clinical and imaging assessments are crucial when genetic resources are limited. This case illustrates that a comprehensive clinical evaluation, including neuroimaging, can support the diagnosis of SCA even without genetic testing. Strategic management emphasizing symptomatic relief and functional improvement through a multidisciplinary approach, including regular follow-up and personalized therapy, are crucial, as evidenced by the timely improvement observed in our case.

CONCLUSION

In resource-limited settings, a comprehensive clinical and neuroimaging assessment is essential for diagnosing spinocerebellar ataxia when genetic testing is not feasible. Effective management through multidisciplinary therapies can improve patient outcomes, underscoring the need for innovative strategies to enhance diagnostic and treatment capabilities in such environments.

摘要

引言

脊髓小脑共济失调(SCA)是一组具有常染色体显性遗传的多样化神经退行性疾病,主要影响小脑及其连接。诊断通常需要进行基因检测,但在资源有限的环境中,临床和神经影像学评估变得至关重要。本病例报告强调了非基因方法在诊断SCA中的作用,并概述了在这种情况下的管理策略。

病例介绍

一名41岁男性,有2年进行性步态失衡、头痛和言语异常病史。他的两个兄弟姐妹有类似症状的家族史,但无重大既往病史。临床检查发现断续性言语、辨距不良和宽基步态。临床和神经影像学检查结果,包括小脑萎缩,在未进行基因检测的情况下导致SCA的诊断。通过言语、职业和物理治疗对患者进行管理,症状逐渐改善。

讨论

SCA以小脑萎缩和一系列临床症状为特征,通常通过基因检测进行诊断,但在基因资源有限时,临床和影像学评估至关重要。本病例表明,即使没有基因检测,包括神经影像学检查在内的全面临床评估也可以支持SCA的诊断。强调通过多学科方法缓解症状和改善功能的战略管理,包括定期随访和个性化治疗,至关重要,我们病例中观察到的及时改善证明了这一点。

结论

在资源有限的环境中,当基因检测不可行时,全面的临床和神经影像学评估对于诊断脊髓小脑共济失调至关重要。通过多学科治疗进行有效管理可以改善患者预后,强调了在这种环境中需要创新策略来提高诊断和治疗能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bba7/11623831/957d91243226/ms9-86-7385-g001.jpg

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