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液体玻璃体活检的分子分析揭示了脑和玻璃体细胞学阴性活检后的隐匿性淋巴瘤。

Molecular Analysis of Liquid Vitreous Biopsy Reveals Occult Lymphoma Following Cytology-Negative Biopsies of the Brain and Vitreous.

机构信息

Department of Ophthalmology and Visual Science, W.K. Kellogg Eye Center, University of Michigan, Ann Arbor, Michigan, USA.

Department of Pathology, University of Michigan, Ann Arbor, Michigan, USA.

出版信息

Ocul Immunol Inflamm. 2024 Oct;32(8):1689-1697. doi: 10.1080/09273948.2023.2287061. Epub 2023 Dec 18.

Abstract

PURPOSE

Primary central nervous system lymphoma (PCNSL) is a rare but deadly malignancy that principally affects adults in the fifth and sixth decades of life. Despite diagnostic advances in analyses of cerebral spinal fluid and neuroimaging, definitive diagnosis of PCNSL requires primary brain tissue biopsy. While small neurosurgical biopsy volumes are pursued to minimize removal of normal brain tissue, the spatial margins to precisely biopsy pathologic tissue are narrow and can result in missed diagnoses. Furthermore, prior steroid treatment can significantly reduce tumor burden increasing the likelihood of a non-diagnostic biopsy.

METHODS

A retrospective case report from a tertiary referral center using a combination of neuroradiological studies, sterotactic tissue biopsy, and molecular testing for genome mutations.

RESULTS

A 72-year-old woman with strong suspicion for PCNSL clinically and radiologically, but cerebral spinal fluid and primary brain tissue biopsy were negative for tumor. However, vitreous liquid biopsy molecular testing for a mutation as well as B-cell clonality ( rearrangement) were positive, indicating the presence of secondary vitreoretinal lymphoma from PCNSL. Only after autopsy of her brain was histopathological and immunohistochemical evidence of PCNSL confirmed.

CONCLUSION

This case illustrates the unique contribution of liquid biopsy neuropathology-oriented molecular testing in a challenging case with high clinical suspicion of PCNSL in which gold-standard diagnostic testing failed to yield a diagnosis.

摘要

目的

原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见但致命的恶性肿瘤,主要影响 50 至 60 岁的成年人。尽管在脑脊液分析和神经影像学方面取得了诊断进展,但 PCNSL 的明确诊断仍需要进行原发性脑组织活检。虽然小神经外科活检量旨在尽量减少正常脑组织的切除,但精确活检病理组织的空间边界很窄,可能导致漏诊。此外,皮质类固醇治疗会显著降低肿瘤负担,增加非诊断性活检的可能性。

方法

回顾性病例报告,来自一个三级转诊中心,采用神经影像学研究、立体定向组织活检和基因突变的分子检测相结合的方法。

结果

一位 72 岁的女性在临床上和放射学上强烈怀疑患有 PCNSL,但脑脊液和原发性脑组织活检均未发现肿瘤。然而,玻璃体液活检的突变和 B 细胞克隆性(重排)分子检测呈阳性,表明存在源自 PCNSL 的继发性玻璃体视网膜淋巴瘤。只有在对她的大脑进行尸检后,才证实了 PCNSL 的组织病理学和免疫组织化学证据。

结论

本病例说明了针对具有高度 PCNSL 临床怀疑的挑战性病例的液体活检神经病理学导向分子检测的独特贡献,而金标准诊断检测未能得出诊断。

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本文引用的文献

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