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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Prolonged interval between sentinel pseudotumoral demyelination and development of primary CNS lymphoma.
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Prolonged interval between sentinel pseudotumoral demyelination and development of primary CNS lymphoma.

机译:前哨假瘤脱髓鞘与原发性中枢神经系统淋巴瘤发展之间的间隔延长。

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摘要

Primary central nervous system lymphoma (PCNSL) can be associated with preceding demyelinating pseudotumoral brain lesions. The 'sentinel' demyelinating lesions recede spontaneously or with corticosteroid, and are followed by development of PCNSL typically within 12 months. This report describes a 29 year-old post-partum woman who developed PCNSL 4 years after a biopsy-proven pseudotumoral demyelinating episode. She presented with focal seizures in February 2005. She subsequently developed hemiparesis and raised intracranial pressure. MRI showed two contrast enhancing lesions in the right frontal lobe, which were hypermetabolic on (18)F-FDG PET. A provisional diagnosis of tumefactive multiple sclerosis was made. Symptoms recurred despite multiple courses of high dose corticosteroid. Brain biopsy confirmed large B-cell non-Hodgkin's lymphoma. This patient illustrates the importance of considering PCNSL in patients presenting with a space-occupying lesion, even with previously confirmed demyelination, and that the interval between the two events may be several years.
机译:原发性中枢神经系统淋巴瘤(PCNSL)可能与先前脱髓鞘的假瘤脑病变有关。 “前哨”脱髓鞘病变会自发地或与皮质类固醇一起后退,然后通常在12个月内发展为PCNSL。该报告描述了一名29岁的产后妇女,在经过活组织检查证实的假瘤脱髓鞘发作4年后发展为PCNSL。她于2005年2月出现局灶性癫痫发作。随后,她出现了偏瘫和颅内压升高。 MRI显示右额叶有两个对比增强病变,在(18)F-FDG PET上代谢亢进。初步诊断为肿瘤性多发性硬化症。尽管多次服用高剂量的皮质类固醇,症状仍会复发。脑活检证实为大B细胞非霍奇金淋巴瘤。该患者说明了即使在先前已确认脱髓鞘的情况下,对于存在占位性病变的患者考虑PCNSL的重要性,并且两次事件之间的间隔可能为数年。

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