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一名小儿肾移植受者在转换为依维莫司治疗后,他克莫司相关臂丛神经炎的恢复——病例报告及文献综述

Recovery of tacrolimus-associated brachial neuritis after conversion to everolimus in a pediatric renal transplant recipient--case report and review of the literature.

作者信息

Al Masri Omar, Fathallah Waseem, Quader Suzanne

机构信息

Department of Pediatrics, Division of Pediatric Nephrology, Sheikh Khalifa Medical City, Abu Dhabi, UAE.

出版信息

Pediatr Transplant. 2008 Dec;12(8):914-7. doi: 10.1111/j.1399-3046.2008.00961.x. Epub 2008 May 23.

Abstract

TAC has been shown to be a potent immunosuppressive agent for solid organ transplantation in pediatrics. Neurotoxicity is a potentially serious toxic effect. It is characterized by encephalopathy, headaches, seizures, or neurological deficits. Here, we describe an eight-and-a-half-yr-old male renal transplant recipient with right BN. MRI demonstrated hyperintense T2 signals in the cervical cord and right brachial plexus roots indicative of both myelitis and right brachial plexitis. Symptoms persisted for three months despite TAC dose reduction, administration of IVIG and four doses of methylprednisolone pulse therapy. Improvement and eventually full recovery only occurred after TAC was completely discontinued and successfully replaced by everolimus.

摘要

他克莫司已被证明是一种用于儿科实体器官移植的强效免疫抑制剂。神经毒性是一种潜在的严重毒性作用。其特征为脑病、头痛、癫痫发作或神经功能缺损。在此,我们描述一名8岁半的男性肾移植受者,患有右侧臂丛神经病变。磁共振成像(MRI)显示颈髓和右侧臂丛神经根T2信号增强,提示存在脊髓炎和右侧臂丛神经炎。尽管降低了他克莫司剂量、给予静脉注射免疫球蛋白(IVIG)以及四次甲泼尼龙冲击治疗,但症状仍持续了三个月。仅在完全停用他克莫司并成功换用依维莫司后,症状才有所改善并最终完全恢复。

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