Bing-Neel综合征-一个具有挑战性的诊断:病例报告

Y. Davidkova, N. Simonoski, B. Spassov, G. Balatzenko, M. Guenova
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引用次数: 0

摘要

Bing-Neel综合征是一种罕见的Waldenström巨球蛋白血症的神经系统并发症,以克隆性淋巴浆细胞浸润中枢神经系统为特征。我们提出一个罕见的临床病例的病人,谁的诊断一年后Waldenström的巨球蛋白血症,进展与多种神经系统的表现和脑脊液累及。诊断基于磁共振成像和流式细胞术检测脑脊液中克隆b细胞。有神经系统症状和Waldenström巨球蛋白血症史的患者应考虑Bing-Neel综合征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bing-Neel Syndrome – A Challenging Diagnosis: Case Report
Bing-Neel syndrome is a rare neurologic complication of Waldenström’s macroglobulinemia, characterized by infiltration of the central nervous system by clonal lymphoplasmacytes. We present a rare clinical case of a patient, who one year after the diagnosis of Waldenström’s macroglobulinemia, progressed with diverse neurologic presentation and cerebrospinal fluid involvement. The diagnosis was based on magnetic resonance imaging and flow cytometry detection of clonal B-cells in the cerebrospinal fluid. Bing-Neel syndrome should be considered in patients with neurologic symptoms and a history of Waldenström’s macroglobulinemia.
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