Myasthenia Crisis as First Presentation of MuSk Positive Myasthenia Gravis: A Case Report.

JNMA; journal of the Nepal Medical Association Pub Date : 2025-03-01 Epub Date: 2025-03-31 DOI:10.31729/jnma.8896
Dipesh Chhetri, Amit Sharma Bhattarai, Pankaj Joshi, Kriti Thapa
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Abstract

We report a unique presentation of a 57-year-old female presented with severe respiratory acidosis, which was found to be a case of Musk-positive Myasthenia Gravis. Patient presented with depressed level of consciousness and respiratory failure, mandating urgent ventilatory support. She responded well with positive pressure ventilation. However, she persistently failed to maintain adequate ventilation after extubation and had to be reintubated. At presentation, the absence of classical symptoms typical of Myasthenia Gravis posed a diagnostic dilemma, initially obscuring the underlying etiology. However, since there was no other identifiable cause for the inability to maintain ventilation, antibody panels were sent which turned out positive for Muscle specific kinase. This case thus highlights the significance of considering atypical neuromuscular presentations, particularly when respiratory compromise is the predominant manifestation, highlighting the necessity for comprehensive neurological evaluation even in the absence of classical symptoms for timely diagnosis and management of Myasthenia Gravis.

麝香阳性重症肌无力首次表现为重症肌无力危象1例。
我们报告一个独特的表现,57岁的女性提出了严重的呼吸性酸中毒,这被发现是一个麝香阳性重症肌无力的情况下。患者表现为意识低下和呼吸衰竭,需要紧急呼吸支持。她在正压通气下反应良好。然而,她拔管后持续不能保持足够的通气,不得不重新插管。目前,缺乏典型的重症肌无力的典型症状提出了一个诊断困境,最初模糊了潜在的病因。然而,由于没有其他可识别的原因导致无法维持通气,抗体小组被送往肌肉特异性激酶阳性。因此,该病例强调了考虑非典型神经肌肉表现的重要性,特别是当呼吸损害是主要表现时,强调了即使在没有经典症状的情况下,也需要进行全面的神经学评估,以便及时诊断和治疗重症肌无力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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