多发性硬化症长期利妥昔单抗治疗相关的鼻-脑毛霉菌病:1例报告和文献回顾

Mohsen Koosha, Golfam Mehrparvar, Sepideh Paybast
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摘要

简介:利妥昔单抗是一种CD20消耗剂,广泛用作治疗多发性硬化症(MS)的标签外疾病治疗(DMT)。本研究旨在报告第一例用利妥昔单抗治疗的继发性进行性多发性硬化症(SPMS)患者的鼻-大脑毛霉菌病。病例报告:患者是一名38岁的男性,有接受利妥昔单抗治疗的SPMS病史,出现亚急性左视力丧失和眼球运动障碍。他还提到了伴随而来的严重头痛和脸颊肿胀。根据脑部和眼眶磁共振成像(MRI)结果,怀疑为鼻-大脑毛霉菌病。随后的内窥镜检查证实了诊断。他接受了两性霉素B脂质体药物治疗和外科清创术,取得了显著的临床康复。他最终出院回家,得到了停用利妥昔单抗的可靠建议。结论:本报告显示一例经利妥昔单抗治疗的SPMS患者并发鼻-脑毛霉菌病。
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Rhino-Sino-Cerebral Mucormycosis Associated with Long-Term Rituximab Therapy in Multiple Sclerosis: A Case Report and Review of the Literature
Introduction: Rituximab is a CD20 depleting agent, widely used as an off-label diseasemodifying treatment (DMT) in treating multiple sclerosis (MS). The present study aimed to report the first case of rhino-sino-cerebral mucormycosis in a patient with secondary progressive MS (SPMS), treated with rituximab. Case Report: The patient was a 38-year-old man with a history of SPMS treated with rituximab, who developed subacute left vision loss and impaired ocular movement. He also mentioned a concomitant severe headache and cheek swelling. Based on the brain and orbital magnetic resonance imaging (MRI) findings, rhino-sino-cerebral mucormycosis was suspected. Subsequent endoscopic examination confirmed the diagnosis. He underwent medical treatment with amphotericin B liposomal and surgical debridement leading to a significant clinical recovery. He was eventually discharged home with a solid recommendation to discontinue rituximab. Conclusion: The present report indicates a case of SPMS treated with rituximab, who developed rhino-sino-cerebral mucormycosis.
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