突发性直立性构音障碍是球源性重症肌无力的主要症状:一个视频病例报告

Dr. Jānis Dāvis Osipovs , Dr. Eva Šankova , Prof. Guntis Karelis , Dr. Ziedīte Želve , Dr. Elīna Polunosika , Mg. sc. sal. Līga Savicka
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引用次数: 0

摘要

重症肌无力(MG)是一种罕见的自身免疫性神经肌肉疾病,可呈现各种早期临床症状和体征。对于神经肌肉疾病经验有限的临床医生来说,诊断伴有球症状的MG在临床上具有挑战性。这个病例报告提出了一个突然发作的直立性构音障碍的老年患者,在诊断的高度怀疑导致短时间内直到确诊。本临床病例为球源性MG患者,在症状出现后第4天开始对症治疗。在住院第11天接受了MG的血清学确认。本病例报告包含一个评估直立性构音障碍的短视频。直立性构音障碍是球源性MG的罕见表现。关于评价直立性构音障碍的信息很少。考虑到球源性MG可能危及生命,我们想分享我们快速诊断和成功治疗的积极经验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sudden onset orthostatic dysarthria as a presenting symptom of bulbar onset myasthenia gravis: a video case report
Myasthenia gravis (MG) is a rare autoimmune neuromuscular disorder that can present with various early clinical symptoms and signs. The diagnosis of MG with bulbar symptom onset can be clinically challenging for clinicians with limited experience with neuromuscular disorders.
This case report presents an elderly patient with an abrupt onset of orthostatic dysarthria, in whom a high level of diagnostic suspicion leads to a short period until confirmation of diagnosis. This clinical case shows symptomatic treatment initiation on the 4th day after the onset of symptoms in a patient with bulbar onset MG. Serologic confirmation of MG was received on the 11th hospitalisation day. This case report contains a short video of the evaluation of orthostatic dysarthria.
Orthostatic dysarthria is a rare presentation symptom for bulbar onset MG. Information on the evaluation of orthostatic dysarthria is sparse. Considering that bulbar onset MG can be a life-threatening condition, we would like to share our positive experience of rapid diagnosis and successful treatment.
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