Vijayakumar B, Cao M, Mackillop L, Sarangmat N, Leite M I, Wathen C G, Nickol A H, Turnbull C D
Department of Respiratory Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Nuffield Department of Clinical Neurosciences, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Obstet Med. 2021 Jun;14(2):121-124. doi: 10.1177/1753495X20944707. Epub 2020 Oct 19.
We describe a 40-year-old female who presented with progressive breathlessness and hypercapnic respiratory failure during pregnancy secondary to undiagnosed muscle-specific kinase myasthenia gravis. Her presentation was progressive and protracted, having over five contacts with healthcare professionals over nine months, many of these predating her pregnancy. Her atypical presentation for myasthenia with minimal limb weakness led to consideration of other causes of hypercapnic respiratory failure. Once diagnosed, she was treated with intravenous immunoglobulin and non-invasive ventilation. She gave birth to a pre-term infant by planned caesarean section. Her insidious presentation and the progressive nature of her breathlessness were unusual and our report highlights the predominant involvement of respiratory muscles in muscle-specific kinase myasthenia. Her pregnancy may have further delayed her diagnosis due the attribution of some symptoms to normal pregnancy. Early recognition and treatment of myasthenia gravis are important to prevent life-threatening complications.
我们描述了一名40岁女性,她在怀孕期间因未被诊断出的肌肉特异性激酶重症肌无力而出现进行性呼吸困难和高碳酸血症性呼吸衰竭。她的症状呈进行性且持续时间长,在九个月内与医疗保健专业人员有过五次以上接触,其中许多接触发生在她怀孕之前。她的重症肌无力表现不典型,肢体无力轻微,这导致人们考虑高碳酸血症性呼吸衰竭的其他原因。一旦确诊,她接受了静脉注射免疫球蛋白和无创通气治疗。她通过计划剖宫产分娩了一个早产儿。她隐匿的表现和呼吸困难的进行性特征并不常见,我们的报告强调了呼吸肌在肌肉特异性激酶重症肌无力中的主要受累情况。由于一些症状被归因于正常妊娠,她的怀孕可能进一步延迟了她的诊断。重症肌无力的早期识别和治疗对于预防危及生命的并发症很重要。