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氟达拉滨神经毒性的临床和影像学特征。

Clinical and imaging features of fludarabine neurotoxicity.

机构信息

Department of Ophthalmology, University of Minnesota, Minneapolis, Minnesota, USA.

出版信息

J Neuroophthalmol. 2010 Mar;30(1):37-41. doi: 10.1097/WNO.0b013e3181ce8087.

Abstract

Neurotoxicity from intravenous fludarabine is a rare but recognized clinical entity. Its brain imaging features have not been extensively described. Three patients received 38.5 mg or 40 mg/m per day fludarabine in a 5-day intravenous infusion before bone marrow transplantation in treatment of hematopoietic malignancies. Several weeks later, each patient developed progressive neurologic decline, including retrogeniculate blindness, leading to coma and death. Brain MRI showed progressively enlarging but mild T2/FLAIR hyperintensities in the periventricular white matter. The lesions demonstrated restricted diffusion but did not enhance. Because the neurotoxicity of fludarabine appears long after exposure, neurologic decline in this setting is likely to be attributed to opportunistic disease. However, the imaging features are distinctive in their latency and in being mild relative to the profound clinical features. The safe dose of fludarabine in this context remains controversial.

摘要

静脉注射氟达拉滨引起的神经毒性是一种罕见但已被认识到的临床病症。其脑部影像学特征尚未得到广泛描述。在进行骨髓移植治疗血液系统恶性肿瘤之前,3 名患者接受了 38.5mg 或 40mg/m 的氟达拉滨,每天静脉输注 5 天。几周后,每位患者都出现了进行性神经功能下降,包括视放射后失明,导致昏迷和死亡。脑部 MRI 显示出进行性扩大但轻度的脑室周围白质 T2/FLAIR 高信号。病变显示受限扩散,但不增强。由于氟达拉滨的神经毒性在暴露后很长时间才出现,因此在此情况下的神经功能下降很可能归因于机会性疾病。然而,其影像学特征在潜伏期和与严重的临床特征相比的轻度方面具有独特性。在此情况下氟达拉滨的安全剂量仍存在争议。

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