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运动神经元病患者出现体重减轻和急慢性呼吸衰竭。

Presentation of motor neuron disease in a patient with weight loss and acute-on-chronic respiratory failure.

机构信息

Acute Medicine, University Hospitals Plymouth NHS Trust, Plymouth, UK

出版信息

BMJ Case Rep. 2021 Apr 21;14(4):e238789. doi: 10.1136/bcr-2020-238789.

Abstract

A previously fit and well 72-year-old man was referred to the acute medical unit with acute shortness of breath and confusion. He had presented 6 months earlier to his General Practitioner with a 6-month history of weight loss and lethargy. Despite CT imaging and extensive blood tests, no cause was found. He was having ongoing outpatient investigations, including a respiratory review leading up to his admission; the deterioration in his condition also coincided with the implementation of the COVID-19 lockdown. On admission, he was found to be in acute-on-chronic type 2 respiratory failure; examination revealed scattered fasciculations. Further inpatient electromyography (EMG) and nerve conduction study (NCS) confirmed motor neuron disease (MND). This case highlighted the importance of considering neuromuscular causes for acute respiratory failure in acute presentations and demonstrated the challenges in the diagnosis of MND in those presenting atypically with non-specific symptoms and the limitations of remote consultations in complex cases.

摘要

一位原本健康的 72 岁男性因急性呼吸急促和意识混乱被转至急症内科。他在 6 个月前曾向他的全科医生就诊,诉有 6 个月的体重减轻和乏力病史。尽管进行了 CT 成像和广泛的血液检查,但未找到病因。他一直在进行门诊检查,包括入院前的呼吸检查;他病情的恶化也与 COVID-19 封锁的实施同时发生。入院时,他被诊断为慢性 2 型呼吸衰竭急性加重;检查发现有散在的束颤。进一步的住院肌电图(EMG)和神经传导研究(NCS)证实为运动神经元病(MND)。本病例强调了在急性发作时考虑急性呼吸衰竭的神经肌肉原因的重要性,并表明在非特异性症状表现不典型的情况下诊断 MND 具有挑战性,以及在复杂病例中远程咨询的局限性。

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