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[宾-尼尔综合征揭示华氏巨球蛋白血症]

[Bing-Neel syndrome revealing Waldenström's macroglobulinemia].

作者信息

Drouet T, Behin A, Psimaras D, Choquet S, Guillevin R, Hoang Xuan K

机构信息

Service de neurologie Mazarin, groupe hospitalier Pitié-Salpêtrière, AP-HP, UPMC, 47, boulevard de l'Hôpital, 75651 Paris cedex 13, France.

出版信息

Rev Neurol (Paris). 2010 Jan;166(1):66-75. doi: 10.1016/j.neurol.2009.03.003. Epub 2009 Apr 28.

Abstract

INTRODUCTION

The most frequent neurological complication of Waldenström's macroglobulinemia is IgM-mediated polyneuropathy. Direct tumor cell infiltration of the nervous system is very rare and better known as the "Bing and Neel syndrome". This syndrome relates usually to a meningeal or meningo-myelo-cerebral tumor infiltration.

OBSERVATION

A 54-year-old man developed a terminal cauda equina syndrome over several years. MRI disclosed lumbar roots infiltration and lumbar puncture the presence of lymphocytic meningitis with intrathecal synthesis of monoclonal IgM identical to that found in the blood. The bone biopsy revealed a lymphoplasmocytic infiltration consistent with the diagnosis of Waldenström's macroglobulinemia. The final diagnosis was meningeal and lumbar roots infiltration revealing Waldenström's macroglobulinemia. Partial remission was obtained after polychemotherapy with CHOP, rituximab and methotrexate. At the end of the treatment, the patient improved his bladder's control and was able to walk with a stick.

DISCUSSION

We reviewed the 35 cases of "Bing and Neel syndrome" we have identified by a PubMed research. The present case report is original by the initial neurological presentation of the disease three years before diagnosis and the successful use of rituximab in the polychemotherapy regimen.

摘要

引言

华氏巨球蛋白血症最常见的神经系统并发症是IgM介导的多发性神经病。肿瘤细胞直接浸润神经系统非常罕见,即众所周知的“宾-尼尔综合征”。该综合征通常与脑膜或脑膜-脊髓-脑肿瘤浸润有关。

观察

一名54岁男性在数年内发展为终末期马尾综合征。磁共振成像(MRI)显示腰神经根浸润,腰椎穿刺显示淋巴细胞性脑膜炎,鞘内合成的单克隆IgM与血液中发现的相同。骨活检显示淋巴浆细胞浸润,符合华氏巨球蛋白血症的诊断。最终诊断为脑膜和腰神经根浸润,提示华氏巨球蛋白血症。采用CHOP、利妥昔单抗和甲氨蝶呤联合化疗后获得部分缓解。治疗结束时,患者膀胱控制能力改善,能够拄着拐杖行走。

讨论

我们通过PubMed检索回顾了我们确定的35例“宾-尼尔综合征”病例。本病例报告的独特之处在于,疾病在诊断前三年出现最初的神经系统表现,以及在联合化疗方案中成功使用了利妥昔单抗。

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