González-Bonet Luis Germán, García-Boyero Raimundo, Gaona-Morales John
Department of Neurosurgery, Hospital General Universitario de Castellón, Castellón, Spain.
Department of Hematology, Hospital General Universitario de Castellón, Castellón, Spain.
World Neurosurg. 2017 Mar;99:808.e1-808.e2. doi: 10.1016/j.wneu.2016.12.122. Epub 2017 Jan 4.
We describe a 71-year-old-patient receiving antiplatelet therapy and being attended by emergency medical services for psychomotor retardation and gait disturbance. An emergency computed tomographic scan showed a bilateral subacute hematoma. The patient reported a fall 2 weeks earlier. We performed bilateral drills and saw a solid mass that was biopsied. The patient had a history of mantle cell lymphoma (MCL) in complete remission (results of bone marrow biopsy and whole-body positron emission tomography-computed tomography scans were normal 6 months earlier). We diagnosed an intracranial MCL by immunohistochemistry, flow cytometry, and fluorescence in situ hybridization. We performed magnetic resonance imaging. The results of a new bone marrow biopsy were positive for recurrence of MCL. MCL constitutes approximately 5%-6% of non-Hodgkin lymphoma. The incidence of central nervous system (CNS) involvement between MCLs is 4.1%. After a review of the literatures we found small series comprising 3-5 cases and a multicenter study with 57 cases. Until now, the median survival was 3.7 months. Ibrutinib, an oral Bruton tyrosine kinase inhibitor, has demonstrated efficacy and CNS penetration in relapsed or refractory MCL with rapid and complete response even after 1 year of follow-up. Our patient received ibrutinib and had a complete response at 3 months, which was maintained to the present (6 months). After a review of the literature, we found different pathologies that can mimic subdural hematomas. However, this is the first report of a lymphoma with CNS involvement mimicking bilateral subdural hematomas. This report contributes to the knowledge of lymphomas with CNS involvement. Its strange radiographic appearance and histologic type make it unique.
我们描述了一名71岁的患者,该患者正在接受抗血小板治疗,因精神运动迟缓及步态障碍而由紧急医疗服务人员接诊。急诊计算机断层扫描显示双侧亚急性血肿。患者称2周前曾摔倒。我们进行了双侧钻孔,发现了一个实性肿块并进行了活检。该患者有套细胞淋巴瘤(MCL)病史,目前处于完全缓解状态(6个月前骨髓活检及全身正电子发射断层扫描-计算机断层扫描结果均正常)。我们通过免疫组织化学、流式细胞术及荧光原位杂交诊断为颅内MCL。我们进行了磁共振成像检查。新的骨髓活检结果显示MCL复发呈阳性。MCL约占非霍奇金淋巴瘤的5%-6%。MCL累及中枢神经系统(CNS)的发生率为4.1%。在查阅文献后,我们发现有包含3-5例病例的小系列报道以及一项有57例病例的多中心研究。截至目前,中位生存期为3.7个月。伊布替尼是一种口服布鲁顿酪氨酸激酶抑制剂,已证明其对复发或难治性MCL有效且可穿透CNS,即使在随访1年后仍能产生快速且完全的反应。我们的患者接受了伊布替尼治疗,3个月时出现完全反应,且一直维持到目前(6个月)。在查阅文献后,我们发现有不同的病理情况可模拟硬膜下血肿。然而,这是首例报道的累及CNS的淋巴瘤模拟双侧硬膜下血肿。本报告有助于增进对累及CNS淋巴瘤的认识。其奇特的影像学表现及组织学类型使其独具特色。