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滤泡性淋巴瘤继发中枢神经系统受累:病例报告及文献复习

Secondary central nervous system involvement by follicular lymphoma: case report and review of the literature.

作者信息

Grupka N L, Seinfeld J, Ryder J, Lillehei K O, Kleinschmidt-Demasters B K

机构信息

Department of Pathology, University of Colorado, Denver, CO 80262, USA.

出版信息

Surg Neurol. 2006 Jun;65(6):590-4. doi: 10.1016/j.surneu.2005.08.027.

Abstract

BACKGROUND

We report a patient with indolent stage IV follicular lymphoma, grade 1, initially successfully treated with chemotherapy, who later developed aggressive diffuse large B-cell lymphoma in the parieto-occipital lobe 8 years after initial presentation. The differing patterns of lymphomatous involvement of the central nervous system (CNS) are briefly reviewed, with a focus on the patterns seen in secondary CNS spread by low-grade lymphomas.

CASE DESCRIPTION

A 53-year-old man was diagnosed with stage IV follicular lymphoma, grade 1, in 1996. Although initial chemotherapy was successful, he developed several recurrences of lymphoma over the following years. In May 2004, he presented with a discrete, single, massive parieto-occipital lobe brain lesion. The mass failed to regress with empiric cranial external beam radiotherapy. Because of suspicion of an unusual infection, the lesion was surgically excised in its entirety. The mass proved to be an aggressive diffuse large B-cell lymphoma, transformed from his previous follicular cell lymphoma, with retention of strong Bcl-2 and Bcl-6 immunoreactivity.

CONCLUSIONS

Parenchymal brain involvement, as opposed to dural or leptomeningeal, is a relatively uncommon pattern of spread to the CNS for systemic lymphomas. More significantly, follicular lymphomas are one of the least frequent types of indolent lymphomas to develop clinically apparent, secondary CNS spread. The presentation of an indolent follicular lymphoma with transformation to an aggressive diffuse large B-cell lymphoma within the brain parenchyma is rare. Its manifestation as a massive, singular lesion is unique and prompted diagnostic confusion.

摘要

背景

我们报告了一名惰性IV期1级滤泡性淋巴瘤患者,最初接受化疗成功,但其在初次就诊8年后于顶枕叶发生了侵袭性弥漫性大B细胞淋巴瘤。本文简要回顾了中枢神经系统(CNS)淋巴瘤累及的不同模式,重点关注低度淋巴瘤继发CNS播散时的模式。

病例描述

一名53岁男性于1996年被诊断为IV期1级滤泡性淋巴瘤。尽管初始化疗成功,但在随后几年中他出现了几次淋巴瘤复发。2004年5月,他出现了一个孤立的、单一的、巨大的顶枕叶脑病变。该肿块在接受经验性颅外照射放疗后未消退。由于怀疑是罕见感染,该病变被完整手术切除。肿块被证实是由先前的滤泡性细胞淋巴瘤转化而来的侵袭性弥漫性大B细胞淋巴瘤,保留了强烈的Bcl-2和Bcl-6免疫反应性。

结论

与硬脑膜或软脑膜受累不同,实质脑受累是系统性淋巴瘤向CNS播散的一种相对不常见的模式。更重要的是,滤泡性淋巴瘤是临床上发生明显继发CNS播散的最不常见的惰性淋巴瘤类型之一。惰性滤泡性淋巴瘤在脑实质内转化为侵袭性弥漫性大B细胞淋巴瘤的情况罕见。其表现为巨大的单一病变是独特的,这引发了诊断上的困惑。

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