肾移植后新发的肌萎缩症

Case Reports in Transplantation Pub Date : 2024-01-29 eCollection Date: 2024-01-01 DOI:10.1155/2024/5473862
Aaron de Souza, Rajesh Raj
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引用次数: 0

摘要

肾移植后新发的肌无力是一种罕见的重症肌无力病。一名 57 岁的女性因患多囊肾而接受腹膜透析治疗,在接受肾移植时使用了标准的巴利昔单抗诱导疗法。她之前没有神经肌肉问题病史。移植三个月后,她出现了进行性乏力和疲劳,最后需要坐轮椅才能行动。移植功能稳定。检查发现她有斑块状肢体无力,反复运动后症状加重。颅神经、反射或感觉均无异常。肌电图正常,但重复神经刺激研究显示,突触后神经肌肉传导缺陷提示患有重症肌无力症。血清学检测没有发现任何抗体。最初使用吡啶斯的明治疗效果不佳。在一次因严重肢体无力而住院治疗后,她接受了静脉注射免疫球蛋白的治疗,病情有了明显好转,并在接下来的几周内持续好转。大约 6 个月后,她的症状再次复发,静脉注射免疫球蛋白后症状再次得到缓解。移植后新发重症肌无力是一种罕见病,在文献中鲜有报道。移植后的免疫抑制通常足以预防免疫介导的疾病,因此这种疾病令人惊讶。这名患者没有类似的病史。肾移植等大手术后身体恢复迟缓通常归因于其他原因,如体质下降,患者通常会接受物理治疗作为应对措施。在这名患者身上,移植手术后持续数周的不明原因的极度虚弱促使他转诊至神经科医生,从而得到了这一罕见的诊断。这个故事强调了密切监测意外症状的必要性,以及在移植后病情改善不符合通常预期时考虑广泛鉴别诊断的必要性。最后,这个病例还说明了多学科参与护理这些复杂病人的好处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
De Novo Onset of Myasthenia Gravis after Kidney Transplantation.

Myasthenia gravis occurring de novo after kidney transplantation is a rare course of severe muscle weakness. A 57-year-old female on treatment with peritoneal dialysis following polycystic kidney disease received a renal transplant with standard basiliximab induction. She had no preceding history of neuromuscular problems. Three months after transplant she presented with progressive weakness and fatigability, finally needing a wheelchair to mobilise. Graft function was stable. Examination revealed patchy limb weakness, worsening on repeated exercise. There were no abnormalities in cranial nerves, reflexes, or sensation. Electromyography was normal, but repetitive nerve stimulation studies showed a postsynaptic neuromuscular transmission defect suggestive of myasthenia gravis. Serological testing revealed no putative antibodies. Initial treatment with pyridostigmine was not tolerated. Following an episode of hospitalisation with severe limb weakness, she received intravenous immunoglobulin and showed dramatic improvement, which persisted over the next few weeks. Approximately 6 months later, she had a relapse of her symptoms, which once again responded to intravenous immunoglobulin therapy. De novo myasthenia gravis after transplantation is a rare entity, infrequently reported in the literature. This illness is surprising since immunosuppression after transplant is usually sufficient to prevent immune-mediated disease. This patient had no history of similar illnesses. Delayed physical recovery after major surgery such as renal transplantation is often attributed to other causes such as deconditioning, and patients are often prescribed physiotherapy as a response. In this patient, the profound unexplained weakness that persisted for several weeks after transplant prompted referral to the neurologist, which enabled this rare diagnosis to be made. This story highlights the need to monitor unexpected symptoms closely and to consider a wide differential diagnosis when improvement after transplant is not along usual expected lines. Finally, this case also illustrates the benefits of multidisciplinary involvement in the care of these complex patients.

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