2021
DOI: 10.7759/cureus.15174
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Pembrolizumab-Associated Seronegative Myasthenia Gravis in a Patient With Metastatic Renal Cell Carcinoma

Abstract: Seronegative myasthenia gravis is a rare, but potential adverse effect of immune checkpoint inhibition. There have been few but increasing number of cases reported in recent years, and early recognition is important for prompt diagnosis and management. Here, we describe the case of a 65-year-old male with metastatic renal cell carcinoma on pembrolizumab diagnosed with new-onset seronegative myasthenia gravis and review literature on its management.

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Cited by 3 publications
(3 citation statements)
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“…One case report demonstrated that the patient developed MG-related symptoms after a second dose of pembrolizumab and was successfully treated with systemic corticosteroid therapy. MG is an autoimmune phenomenon characterized by fluctuating muscle weakness involving ocular, bulbar, respiratory and limb muscles [ 9 ]. MG is diagnosed based on typical symptoms and positive serum antibodies.…”
Section: Discussionmentioning
confidence: 99%
“…One case report demonstrated that the patient developed MG-related symptoms after a second dose of pembrolizumab and was successfully treated with systemic corticosteroid therapy. MG is an autoimmune phenomenon characterized by fluctuating muscle weakness involving ocular, bulbar, respiratory and limb muscles [ 9 ]. MG is diagnosed based on typical symptoms and positive serum antibodies.…”
Section: Discussionmentioning
confidence: 99%
“…Though MG can independently manifest as a paraneoplastic syndrome, the association with de novo diagnosis after starting pembrolizumab suggests a likely checkpoint-inhibitor-associated presentation of MG [ 3 ]. Our patient developed symptoms consistent with myasthenia gravis shortly after being treated with pembrolizumab, which included ptosis, dysarthria, cervical myalgia, generalized fatigue, and weakness.…”
Section: Discussionmentioning
confidence: 99%
“…Due to clinical concern for ICI neurotoxicity, methylprednisolone was initiated (1 g intravenously daily for five days) [ 2 , 7 ]. Ultimately the clinical picture was thought to be most consistent with seronegative MG [ 7 , 9 ]. Since the patient exhibited fluctuating weakness, other causes including inflammatory myopathy and acute inflammatory demyelinating polyradiculoneuropathy were considered less likely.…”
Section: Case Presentationmentioning
confidence: 99%