Finessi Andrea, Aziz Muhammad A, Izquierdo-Pretel Guillermo, Bracho Adriana
Internal Medicine, Florida International University, Herbert Wertheim College of Medicine, Miami, USA.
Cureus. 2024 Apr 14;16(4):e58230. doi: 10.7759/cureus.58230. eCollection 2024 Apr.
We present a case of cytomegalovirus (CMV) polyradiculopathy which occurred concomitantly with CMV encephalitis and CMV retinitis in a patient with HIV/AIDS. Our patient is a 43-year-old male who was admitted with progressive changes in mentation. Cerebrospinal fluid (CSF) analysis showed elevated white blood cell (WBC), low glucose, and elevated protein. The polymerase chain reaction (PCR) panel of CSF was positive for CMV, and other microbiology results were negative. Extensive bilateral CMV retinitis was also noted. The patient was started on ganciclovir and foscarnet, and two weeks after, highly active antiretroviral therapy (HAART) was initiated using Truvada and dolutegravir. The hospital course was complicated by urinary retention and bilateral lower extremity weakness with hypotonia, severe hyperalgesia, and allodynia. An electromyography (EMG) study demonstrated bilateral lumbosacral root dysfunction at L2-S1 with active neurologic changes indicating significant axon loss. Neurology was consulted, and the patient was diagnosed with CMV-induced polyradiculopathy. After three months of treatment, no improvement was noted on lower limbs as he continued with intravenous (IV) ganciclovir. The therapeutic response to induction therapy was discordant as improvement of encephalitis was noted, but not on polyradiculopathy after 180 days of treatment. This highlights the lack of data and treatment guidelines for established CMV polyradiculopathy and not only the necessity for prolonged treatment of CMV polyradiculopathy but also the difficulty in recovery of function once it has developed.
我们报告一例巨细胞病毒(CMV)多发性神经根病病例,该病例发生在一名患有人类免疫缺陷病毒/获得性免疫综合征(HIV/AIDS)的患者身上,同时伴有CMV脑炎和CMV视网膜炎。我们的患者是一名43岁男性,因精神状态进行性改变入院。脑脊液(CSF)分析显示白细胞(WBC)升高、葡萄糖降低和蛋白质升高。CSF的聚合酶链反应(PCR)检测结果显示CMV呈阳性,其他微生物学检查结果均为阴性。还发现广泛的双侧CMV视网膜炎。患者开始接受更昔洛韦和膦甲酸钠治疗,两周后,开始使用替诺福韦酯和多替拉韦进行高效抗逆转录病毒治疗(HAART)。住院过程中出现了尿潴留以及双侧下肢无力,伴有肌张力减退、严重痛觉过敏和感觉异常。肌电图(EMG)研究显示L2-S1水平双侧腰骶神经根功能障碍,伴有活跃的神经学改变,提示明显的轴突丢失。咨询了神经科医生后,患者被诊断为CMV诱导的多发性神经根病。经过三个月的治疗,患者继续静脉注射(IV)更昔洛韦,但下肢情况未见改善。诱导治疗的疗效不一致,因为在治疗180天后,脑炎有所改善,但多发性神经根病没有改善。这突出了对于已确诊的CMV多发性神经根病缺乏数据和治疗指南的情况,不仅强调了对CMV多发性神经根病进行长期治疗的必要性,也凸显了一旦病情发展,功能恢复的困难。