Inzirillo Karen, Carranza Octavio, Swerdloff Marc A
Neurology, Marcus Neuroscience Institute, Boca Raton Regional Hospital, Baptist Health South Florida, Boca Raton, USA.
Neurology, Charles E. Schmidt College of Medicine, Florida Atlantic University, Boca Raton, USA.
Cureus. 2024 Nov 29;16(11):e74768. doi: 10.7759/cureus.74768. eCollection 2024 Nov.
Myasthenia gravis (MG) is one of the most common neuromuscular disorders. It is an antibody-mediated autoimmune disease affecting the neuromuscular junction, presenting with fluctuating muscle weakness that commonly affects the ocular, bulbar, proximal, and respiratory muscles. Treating MG in the older population with preexisting comorbidities can be challenging. Intravenous efgartigimod alfa (EA) was successfully used as an initial monotherapy for a 90-year-old woman with acetylcholine receptor seropositive MG and stage IV colon adenocarcinoma who was referred for visually disabling bilateral eyelid ptosis. Standard MG therapy was considered but not chosen due to relative contraindications and anticipated adverse effects. EA infusions were well tolerated and corrected her ptosis after two weeks of treatment. EA infusion may be considered the first-line therapy for selected patients with seropositive generalized MG who have disabling ocular symptoms.
重症肌无力(MG)是最常见的神经肌肉疾病之一。它是一种抗体介导的自身免疫性疾病,影响神经肌肉接头,表现为波动性肌无力,通常影响眼肌、延髓肌、近端肌和呼吸肌。治疗合并有其他疾病的老年重症肌无力患者具有挑战性。静脉注射艾加莫德α(EA)成功地用作一名90岁女性的初始单一疗法,该女性患有乙酰胆碱受体血清阳性重症肌无力和IV期结肠腺癌,因双侧眼睑下垂导致视力障碍前来就诊。考虑过标准的重症肌无力疗法,但由于相对禁忌证和预期的不良反应而未选用。EA输注耐受性良好,治疗两周后矫正了她的上睑下垂。对于有导致视力障碍的眼部症状的血清阳性全身型重症肌无力的特定患者,EA输注可被视为一线治疗方法。