[一名全身性肌无力患者出现了 COVID 19 相关肺炎,而 Eculizumab 为患者带来了有益的临床疗程]。

Q4 Medicine Clinical Neurology Pub Date : 2024-02-23 Epub Date: 2024-01-27 DOI:10.5692/clinicalneurol.cn-001922
Yusuke Kuroda, Gennya Watanabe, Kazuki Satou, Hirohiko Ono, Kennichi Tsukita, Yasushi Suzuki
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引用次数: 0

摘要

一位 74 岁的妇女在 32 岁时患上了肌无力(MG)。次年,她接受了胸腺瘤切除手术,但她的肌萎缩症状并未稳定,需要经常住院接受速效治疗(FT)。两年前的 3 月,她开始使用依库珠单抗,并在 MG 症状变轻后接受了门诊随访。今年 2 月,她因轻度 COVID-19 相关肺炎、全身不适和发热而住进我院。她的 COVID-19 相关性肺炎接受了静脉注射索托维单抗、地塞米松和非分细肝素的治疗,而 MG 的口服治疗则保持不变。住院期间没有使用伊库珠单抗,原因是该患者的 MG 症状稳定,而且日本的保险制度不支付该药物的费用。住院期间,患者的 MG 和 COVID-19 相关肺炎并不严重。然而,当 MG 患者出现 COVID-19 相关肺炎时,发生肌无力危象和死亡的风险很高。多份报告显示,接受依库珠单抗治疗的 MG 患者发生 COVID-19 相关肺炎的情况并不严重,而且依库珠单抗对补体途径的抑制对 COVID-19 相关肺炎有效。在 COVID-19 患者的器官微血管中观察到补体沉积,这表明补体过载可能是 COVID-19 相关肺炎的一个危险因素。补体过度激活可能与发病机制有关;因此,依库珠单抗可能通过抑制这一途径发挥作用。在本病例中,患者在患 COVID-19 相关肺炎期间停用了依库珠单抗,但在因 COVID-19 相关肺炎住院期间,作为补体指标的 CH50 却受到了抑制。因此,依库珠单抗可能干扰了这一病程。本病例表明,依库珠单抗对合并 COVID-19 相关肺炎的 MG 患者可能是安全的,患者也可以耐受,但还需要积累更多的病例来支持这一结论。
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[Eculizumab led to beneficial clinical course in a patient with generalized myasthenia gravis who developed COVID 19-associated pneumonia].

A 74-year-old woman developed myasthenia gravis (MG) at the age of 32. She had a thymoma removed the following year, but her MG symptoms did not stabilize, and she required frequent hospitalization for fast-acting treatment (FT). She started eculizumab in March of two years ago and was followed up on an outpatient basis as her MG symptoms became milder. In February of this year, she was admitted to our hospital due to mild COVID-19-associated pneumonia with general malaise and fever. Her COVID-19-associated pneumonia was treated with intravenous sotrovimab, dexamethasone, and unfractionated heparin, and oral therapy for MG stayed the same. Eculizumab was not administered during hospitalization due to the combination of stable MG symptoms and the fact that the drug is not paid for by the Japanese insurance system. The patient's MG and COVID-19-associated pneumonia were not severe during hospitalization. However, the risk of myasthenic crisis and death is high when patients with MG develop COVID-19-associated pneumonia. Several reports suggest that the condition of patients with eculizumab-treated MG who develop COVID-19-associated pneumonia is not severe, and that that inhibition of the complement pathway with eculizumab is effective for COVID-19-associated pneumonia. Complement deposition in organ microvessels has been observed in patients with COVID-19, which suggests that complement overload may be a risk factor for COVID-19-associated pneumonia. Excessive complement activation may be involved in the pathogenesis; thus, eculizumab may function by inhibiting this pathway. In this case, eculizumab was discontinued while the patient had COVID-19-associated pneumonia, however, CH50, which is an indicator of complement, was suppressed during hospitalization due to the COVID-19-associated pneumonia. Therefore, eculizumab may have interfered with this course of events. This case demonstrates that eculizumab may be safe for and tolerated by patients with MG and COVID-19-associated pneumonia, but more cases need to be accumulated to support this conclusion.

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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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