Rizvi Wajeeha, Truong Quoc
Internal Medicine, University of Kansas School of Medicine - Wichita.
Cureus. 2018 Feb 9;10(2):e2176. doi: 10.7759/cureus.2176.
Chronic lymphocytic leukemia (CLL) is the most prevalent leukemia with over 20,000 estimated cases in 2017. Leukemic involvement of the nervous system from CLL causing neurologic symptoms is reported in only about one percent of patients. Unfortunately, there is no current standard therapy for the treatment of CLL leptomeningeal disease. In this case, we discuss an unusual presentation of CLL leptomeningeal disease misdiagnosed as chronic rebound headache. A 61-year-old female was diagnosed with Rai stage I CLL in 2002. She presented at that time with peripheral blood lymphocytosis and subsequent flow cytometry revealed a mature B cell population consistent with CLL. She was monitored clinically as there were no indications for therapy. In 2006, she developed B symptoms along with hemolytic anemia refractory to steroids and was initiated on chemotherapy with fludarabine, cyclophosphamide, and rituximab (FCR). She had a complete response after six cycles. The patient was in her usual state of health until 2016, when she complained of chronic headaches. She took acetaminophen and ibuprofen regularly and was diagnosed with rebound headaches by neurology. These symptoms progressed and the patient developed encephalopathy requiring inpatient admission. Magnetic resonance imaging (MRI) revealed abnormal enhancement in the cerebellar peduncles and dentate nuclei symmetrically; a lumbar puncture performed revealed evidence of CLL consistent with leptomeningeal disease. Therapy was started with oral ibrutinib at 560 mg daily for better central nervous system (CNS) penetration. After three months of therapy, she had complete resolution of symptoms and MRI abnormalities. Leptomeningeal disease is a rare complication of CLL that clinicians should be aware of and ibrutinib can be an effective, tolerable therapy for this debilitating disease.
慢性淋巴细胞白血病(CLL)是最常见的白血病,2017年估计病例超过20000例。据报道,仅约1%的CLL患者会出现白血病累及神经系统并导致神经症状。不幸的是,目前尚无治疗CLL软脑膜疾病的标准疗法。在此病例中,我们讨论了一例被误诊为慢性反弹性头痛的CLL软脑膜疾病的不寻常表现。一名61岁女性于2002年被诊断为Rai I期CLL。她当时表现为外周血淋巴细胞增多,随后的流式细胞术显示为与CLL一致的成熟B细胞群。由于没有治疗指征,她接受了临床监测。2006年,她出现了B症状以及对类固醇难治的溶血性贫血,并开始接受氟达拉滨、环磷酰胺和利妥昔单抗(FCR)化疗。六个周期后她完全缓解。该患者一直处于健康状态,直到2016年,她开始抱怨慢性头痛。她定期服用对乙酰氨基酚和布洛芬,并被神经科诊断为反弹性头痛。这些症状逐渐加重,患者发展为脑病,需要住院治疗。磁共振成像(MRI)显示小脑脚和齿状核对称异常强化;腰椎穿刺显示有与软脑膜疾病一致的CLL证据。开始使用每日560毫克的口服伊布替尼进行治疗,以更好地穿透中枢神经系统(CNS)。治疗三个月后,她的症状和MRI异常完全消失。软脑膜疾病是CLL的一种罕见并发症,临床医生应予以关注,伊布替尼可以是治疗这种使人衰弱疾病的一种有效且可耐受的疗法。