Pham Chengde, Griffiths James D, Kam Anthony, Hunn Martin K
Department of Neurosurgery, Level 1, Old Baker Building, The Alfred Hospital, 55 Commercial Rd, Melbourne, Victoria 3004, Australia.
Melbourne Haematology, Epworth Medical Centre, Suite 1.6, 173 Lennox St, Richmond, Victoria 3121, Australia.
J Clin Neurosci. 2017 Nov;45:134-135. doi: 10.1016/j.jocn.2017.07.010. Epub 2017 Jul 29.
We report the case of a 68-year-old male with right eye vision loss secondary to a compressive optic neuropathy from Waldenstrom macroglobulinaemia relapse in both cavernous sinuses. Central nervous system involvement is extremely uncommon in lymphoplasmacytic lymphoma. Known as Bing-Neel syndrome, this has not been previously reported to present simultaneously in bilateral cavernous sinuses. We discuss the pathophysiology, diagnostic and neuroradiological features of Bing-Neel syndrome. In this case, there was marked clinical and radiological response to chemotherapy. As outcomes following treatment for Waldenstrom macroglobulinaemia improve, greater awareness of its less common manifestations becomes important. Neurosurgical intervention may be indicated to obtain histological diagnosis or decompress critical structures.
我们报告了一例68岁男性患者,因双侧海绵窦内瓦尔登斯特伦巨球蛋白血症复发导致压迫性视神经病变而出现右眼视力丧失。中枢神经系统受累在淋巴浆细胞淋巴瘤中极为罕见。这种情况被称为宾-尼尔综合征,此前尚未有双侧海绵窦同时出现的报道。我们讨论了宾-尼尔综合征的病理生理学、诊断及神经放射学特征。在此病例中,化疗后有明显的临床和影像学反应。随着瓦尔登斯特伦巨球蛋白血症治疗效果的改善,对其较罕见表现的更多认识变得很重要。可能需要进行神经外科干预以获得组织学诊断或对关键结构进行减压。