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一名接受类固醇和利妥昔单抗治疗的重症肌无力患者的咳嗽变异性哮喘

Cough-Variant Asthma in a Myasthenia Gravis Patient on Treatment With Steroids and Rituximab.

作者信息

Meshram Shailesh B, Anand Atulya, Orakkan Rishi G

机构信息

Respiratory Medicine, Dr. D. Y. Patil Medical College, Hospital & Research Centre, Dr. D. Y. Patil Vidyapeeth (Deemed to be University), Pune, IND.

出版信息

Cureus. 2024 Oct 15;16(10):e71512. doi: 10.7759/cureus.71512. eCollection 2024 Oct.

DOI:10.7759/cureus.71512
PMID:39544556
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11561697/
Abstract

Muscle weakness that worsens on exercise and improves on resting is the hallmark of myasthenia gravis (MG), an uncommon autoimmune illness. Acetylcholinesterase inhibitors, immunosuppressants, and corticosteroids are commonly used in treatment. Rituximab has been tried in refractory patients. On the contrary, asthma is characterized by a persistent inflammation of the airways and a range of symptoms, including cough-variant asthma (CVA), in which the main symptom is only cough. We describe the case of a female in her 30s who had a history of MG and had been treated with steroids and rituximab. The patient had an acute dry cough in bouts. Spirometry revealed no obstructive or restrictive pattern, and the chest X-ray was normal. Based on allergy diathesis, a diagnosis of CVA was hypothesized and confirmed clinically by the patient's reaction to long-acting beta-agonists and inhaled corticosteroids. This case emphasizes how difficult it can be to diagnose respiratory symptoms in MG patients and how crucial it is to rule out CVA as a differential diagnosis, particularly in patients who have recently started immunomodulatory medication and have an allergy tendency. Fast symptom relief and positive clinical results were achieved by the efficient use of inhalation treatment.

摘要

运动时肌无力加重、休息时肌无力改善是重症肌无力(MG)的典型特征,这是一种罕见的自身免疫性疾病。乙酰胆碱酯酶抑制剂、免疫抑制剂和皮质类固醇常用于治疗。利妥昔单抗已用于难治性患者。相反,哮喘的特征是气道持续炎症和一系列症状,包括咳嗽变异性哮喘(CVA),其主要症状仅为咳嗽。我们描述了一名30多岁女性的病例,她有重症肌无力病史,曾接受类固醇和利妥昔单抗治疗。患者阵发性急性干咳。肺功能检查未显示阻塞性或限制性模式,胸部X光片正常。基于过敏体质,推测为咳嗽变异性哮喘诊断,并通过患者对长效β受体激动剂和吸入性皮质类固醇的反应在临床上得到证实。该病例强调了重症肌无力患者呼吸症状诊断的困难程度,以及排除咳嗽变异性哮喘作为鉴别诊断的关键,特别是在最近开始使用免疫调节药物且有过敏倾向的患者中。通过有效使用吸入治疗实现了快速症状缓解和积极的临床结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/888e/11561697/b7b8bb0eda84/cureus-0016-00000071512-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/888e/11561697/8f501da8ad6c/cureus-0016-00000071512-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/888e/11561697/e8caabd5e5b3/cureus-0016-00000071512-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/888e/11561697/b7b8bb0eda84/cureus-0016-00000071512-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/888e/11561697/8f501da8ad6c/cureus-0016-00000071512-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/888e/11561697/e8caabd5e5b3/cureus-0016-00000071512-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/888e/11561697/b7b8bb0eda84/cureus-0016-00000071512-i03.jpg

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本文引用的文献

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Myasthenia gravis, respiratory function, and respiratory tract disease.重症肌无力、呼吸功能与呼吸道疾病。
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