From the 2nd Radiology Department, University Hospital of Strasbourg, Avenue Molière 1, 67098, Strasbourg, France.
Division of Neuroradiology, Department of Imaging and Medical Information Sciences, Geneva University Hospitals, Rue Gabrielle-Perret-Gentil 4, 1205, Geneva, Switzerland.
Eur Radiol. 2019 Jan;29(1):102-114. doi: 10.1007/s00330-018-5543-7. Epub 2018 Jun 19.
Bing-Neel syndrome (BNS) is a rare neurological complication of Waldenström's macroglobulinemia. The aim of this study is to describe the spectrum of radiological manifestations of this syndrome and their prevalence in order to facilitate its early diagnosis.
Twenty-four patients with BNS were diagnosed between 1994 and 2016 in eight centres in France. We retrospectively examined the medical records of these patients as well as the corresponding literature, focusing on imaging studies. Recorded data were statistically analysed and radiological findings described.
The mean age of our patients was 62.4 years (35-80 years). The vast majority of patients were men, with a male to female ratio of 9:1. Findings included parenchymal or meningeal involvement or both. The most common finding was leptomeningeal infiltration, either intracranial or spinal, with a prevalence reaching 70.8%. Dural involvement was present in 37.5% of patients. In 41.7% (10/24) of patients, there was parenchymal involvement with a higher prevalence of brain comparing to medullar involvement (33.3% and 23.1% respectively). High T2 signal of the parenchyma was identified in 41.7% of patients and high signal in diffusion was evident in 25% of them. Intraorbital or periorbital involvement was also detected in four cases. A proposition regarding the appropriate imaging protocol completed our study.
BNS's diagnosis remains challenging. Central nervous system MRI findings in the setting of known or suspected Waldenström's macroglobulinemia appear to be highly suggestive of BNS and appropriate imaging protocols should be implemented for their depiction.
• Diagnosis of Bing-Neel syndrome (BNS) remains challenging and recent expert recommendations include MRI in the diagnostic criteria for the syndrome. • The most common radiological manifestations of BNS are leptomeningeal/dural infiltration or parenchymal involvement of brain or spinal cord, but many atypical forms may exist with various presentations. • Appropriate imaging protocol for BNS should include enhanced MRI studies of both brain and spine.
Bing-Neel 综合征(BNS)是瓦尔登斯特伦巨球蛋白血症的一种罕见神经系统并发症。本研究旨在描述该综合征的放射学表现谱及其在疾病中的普遍性,以便于早期诊断。
1994 年至 2016 年期间,法国 8 个中心共诊断出 24 例 BNS 患者。我们回顾性地检查了这些患者的病历及相关文献,重点关注影像学检查。记录的数据进行了统计学分析,并描述了放射学发现。
患者的平均年龄为 62.4 岁(35-80 岁)。绝大多数患者为男性,男女比例为 9:1。表现包括实质或脑膜受累或两者均有。最常见的表现是脑脊髓膜浸润,颅内或脊髓均可发生,发生率为 70.8%。37.5%的患者存在硬脑膜受累。24 例患者中有 41.7%(10/24)存在实质受累,脑实质受累的发生率高于脊髓实质受累(分别为 33.3%和 23.1%)。41.7%的患者存在实质高 T2 信号,25%的患者存在弥散高信号。4 例患者还存在眼眶或眶周受累。本研究还提出了一个关于适当影像学检查方案的建议。
BNS 的诊断仍然具有挑战性。已知或疑似瓦尔登斯特伦巨球蛋白血症患者的中枢神经系统 MRI 发现似乎高度提示 BNS,应实施适当的成像方案来描绘其特征。
• Bing-Neel 综合征(BNS)的诊断仍然具有挑战性,最近的专家建议将 MRI 纳入该综合征的诊断标准。• BNS 最常见的放射学表现是脑膜/硬脑膜浸润或脑或脊髓实质受累,但可能存在多种不典型表现,具有多种表现形式。• BNS 的适当成像方案应包括脑和脊柱增强 MRI 研究。