Haboubacar Idi Djibadje, Kaoutar El Fakhr, Musoni Liberat, Ezzouine Hanane, Charra Boubaker
Medical Intensive Care Unit, Ibn Rochd University Hospital, B.P 5696, Casablanca, Morocco.
Faculty of Medicine and Pharmacy, Hassan II University of Casablanca, Morocco.
Ann Med Surg (Lond). 2021 Sep 4;69:102809. doi: 10.1016/j.amsu.2021.102809. eCollection 2021 Sep.
Introduction and importance: Myasthenia gravis is an autoimmune disease characterized by the destruction of postsynaptic acetylcholine receptors in skeletal striated muscles. It is most common in young women. Myasthenia can be diagnosed by the detection of anti-acetylcholine receptor antibodies. Treatment includes anticholinesterase drugs, thymectomy, and restricting drugs that may aggravate myasthenia. The authors report a rare case of accidental revelation of myasthenia gravis in an elderly woman during sedation for diagnostic gastrointestinal fibroscopy. : A 85-years-old female patient scheduled for diagnostic gastrointestinal fibroscopy presented signs of myasthenic crisis during the perioperative with severe respiratory failure. The diagnosis of myasthenia was confirmed by bioassay and electromyogram (EMG). Her chest CT scan showed a thymoma. The evolution was favorable as a result of early and appropriate management. Myasthenia can occur in perioperative settings outside the usual circumstances. The prognosis depends on early and adapted management.
重症肌无力是一种自身免疫性疾病,其特征是骨骼肌横纹肌突触后乙酰胆碱受体遭到破坏。该病在年轻女性中最为常见。重症肌无力可通过检测抗乙酰胆碱受体抗体来诊断。治疗方法包括抗胆碱酯酶药物、胸腺切除术以及停用可能加重重症肌无力的药物。作者报告了一例罕见病例,一名老年女性在诊断性胃肠纤维镜检查镇静期间意外被发现患有重症肌无力。:一名85岁女性患者计划进行诊断性胃肠纤维镜检查,在围手术期出现重症肌无力危象并伴有严重呼吸衰竭。通过生物测定和肌电图(EMG)确诊为重症肌无力。她的胸部CT扫描显示有胸腺瘤。由于早期和适当的治疗,病情进展良好。重症肌无力可在通常情况以外的围手术期发生。预后取决于早期和适当的治疗。