65岁女性迟发性重症肌无力伴强力霉素长期使用的罕见病例

Angel Wong, Kayvan Mirhadi
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摘要

重症肌无力(MG)是一种罕见的自身免疫性疾病,由抗体介导的乙酰胆碱受体(AChR)或其相关蛋白的破坏引起。MG发病年龄呈双峰分布,在第二、三十年以女性病例为主,在第六、八十年以男性病例为主。MG经常被压力源(如全身性疾病、药物、手术和怀孕)所掩盖。我们提出了一例迟发性MG在65岁的女性与长期使用强力霉素最近的历史。然而,她过去的一些病史,包括涉及免疫系统的合并症和许多药物不耐受,应该增加临床对MG的怀疑。此外,在症状出现之前的一个医学事件是用强力霉素治疗肺炎。本病例提示,MG患者应谨慎使用强力霉素,对于有神经系统症状和既往病史的老年女性患者,MG应作为鉴别诊断的一部分。
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Rare Case of Late-onset Myasthenia Gravis in a 65-year-old Female with Prolonged Doxycycline Use
Myasthenia gravis (MG) is a rare autoimmune condition caused by antibody-mediated disruption of acetylcholine receptors (AChR) or their associated proteins. The age of onset of MG has a bimodal distribution, with a predominance of female cases in the second and third decades and a predominance of male cases in the sixth to eighth decades. MG is often unmasked by stressors such as systemic illness, medication, surgery, and pregnancy. We present a case of late-onset MG in a 65-year-old female with a recent history of prolonged doxycycline use. However, there are aspects of her past medical history, including comorbidities involving the immune system and numerous drug intolerances that should have increased clinical suspicion for MG. Additionally, one medical event that preceded symptom onset was pneumonia treated with doxycycline. This case suggests that doxycycline should be used with caution in MG patients, and that MG should be considered as part of the differential diagnosis in older female patients presenting with neurologic symptoms and suggestive past medical history.
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