非典型神经淋巴瘤1例

Laura Danielson, MD, Ann Murray, MD, Kymberly A. Gyure, MD, Amelia Adcock, MD
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摘要

神经淋巴瘤的诊断是非常具有挑战性的,需要高度的怀疑。本文讨论一例继发性神经淋巴瘤的临床及随访。有弥漫性大b细胞淋巴瘤病史的患者表现为急性、上升、进行性神经病变,与急性炎性脱髓鞘性多根神经病变相似,但有细微差别。静脉注射免疫球蛋白无反应,但在同时进行血浆置换和口服类固醇后有短暂的改善。广泛的检查最终通过腓肠神经活检诊断为神经淋巴瘤。根据家属的意愿,病人在开始目前典型的化疗药物治疗前,被送往安宁疗护中心。神经淋巴瘤可以表现为一种快速进展的神经病变,诊断上具有挑战性,然而,关于治疗方案的数据有限。多个病例报告表明,包括大剂量甲氨蝶呤在内的化疗组合取得了令人鼓舞的结果。
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An Atypical Case of Neurolymphomatosis
The diagnosis of neurolymphomatosis can be highly challenging requiring a high index of suspicion. This paper discusses a clinical case and workup for secondary neurolymphomatosis. A patient with history of diffuse large B-cell lymphoma presented as an acute, ascending, progressive neuropathy mimicking acute inflammatory demyelinating polyradiculopathy with subtle differences. No response to intravenous immunoglobulins was seen though he had transient improvement after concurrent plasmapheresis and oral steroids. Extensive work-up eventually lead to a diagnosis of neurolymphomatosis by sural nerve biopsy. The patient was sent to hospice per family preference prior to initiation of the typical current treatment of chemotherapeutic agents. Neurolymphomatosis can present as a rapidly progressive neuropathy that can be diagnostically challenging, however, data is limited regarding treatment protocols. Multiple case reports suggest encouraging results from chemotherapy combinations which include high-dose methotrexate.
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