Tallant Aaron, Selig Daniel, Wanko Sam O, Roswarski Joseph
Walter Reed National Military Medical Center, Bethesda, Maryland, USA.
Tripler Army Medical Center, Honolulu, Hawaii, USA.
BMJ Case Rep. 2018 Oct 2;2018:bcr-2018-226102. doi: 10.1136/bcr-2018-226102.
The authors present a case of an elderly man with a history of Waldenstrom macroglobulinaemia in remission who presented with progressively worsening gait abnormalities and falls for several months. His examination was notable for bilateral lower extremity weakness and an unsteady gait. Brain and spinal MRI showed focal leptomeningeal enhancement in the brain and spinal column. Lumbar puncture was performed and cerebrospinal fluid flow cytometry demonstrated a monoclonal CD5/CD10-negative, CD20-positive B-cell lymphocyte population consistent with a diagnosis of Bing-Neel syndrome. He was started on ibrutinib, an oral Bruton's tyrosine kinase inhibitor, and had marked improvement in his weakness and gait. Repeat imaging 2 months after starting ibrutinib showed improvement in his leptomeningeal enhancement. During subsequent follow-up, he continued to tolerate ibrutinib and had a sustained clinical response.
作者报告了一例既往有处于缓解期的华氏巨球蛋白血症病史的老年男性病例,该患者出现进行性加重的步态异常和跌倒数月。他的检查结果显示双侧下肢无力和步态不稳。脑部和脊髓磁共振成像(MRI)显示脑部和脊柱的软脑膜有局灶性强化。进行了腰椎穿刺,脑脊液流式细胞术显示存在单克隆CD5/CD10阴性、CD20阳性B淋巴细胞群,符合宾-尼尔综合征的诊断。他开始服用口服布鲁顿酪氨酸激酶抑制剂伊布替尼,其虚弱症状和步态有显著改善。开始服用伊布替尼2个月后复查影像学检查显示其软脑膜强化有所改善。在随后的随访中,他继续耐受伊布替尼并获得了持续的临床反应。