Department of Neurology, College of Health Sciences, Addis Ababa University, Po Box 6396, Addis Ababa, Ethiopia.
Department of Internal Medicine, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
BMC Infect Dis. 2020 Aug 5;20(1):574. doi: 10.1186/s12879-020-05297-9.
Despite widespread use of combination antiretroviral therapy (cART), HIV-associated neurocognitive disorder (HAND) and HIV-associated myelopathy (HAM) are not showing significant reduction in there occurrence. The HAM is a progressive myelopathy that often occur synchronously with severe form of the HAND in patients' having advanced immunosuppression. However, co-existence of less severe form of the HAND and HAM in patient with relatively preserved CD4 cells is rarely reported clinical entity in post cART era.
We report a 16-year old male, acquired HIV infection vertically, was on second line regimen because of virological failure since 3 years. His current CD4 lymphocyte count is 835 cells/uL with viral RNA level of 33,008 copies/mL. Currently presented with progressive forgetfulness, gait imbalance, and a frequent staring episodes without loss of postural tone. Neurological examination was pertinent for cognitive dysfunction with score of 6 on International HIV Dementia Scale (motor speed = 3, psychomotor speed = 2, and memory recall = 1). Lower limbs power is 4/5, increased deep tendon reflexes, and unsteady gait. Brain MRI revealed diffuse both cortical and white matter T2 and FLAIR hyperintense lesions. Thoracic MRI showed abnormal T2 signal prolongation spanning from mid thoracic cord to conus. Electroencephalography study showed severe generalized slowing with evidence of focal dysrhythmia in bilateral frontotemporal regions. Unremarkable serum vitamin B 12 level (286 ng/mL). Virological failure with the HAND, HAM and seizure was considered. Dolutegravir +3TC + ATV/r regimen and valproate for seizure disorder was started. On 6 months follow up evaluation, he is clinically stable with significant improvement of his symptoms related to seizure disorders and modest improvement of his cognitive dysfunction, as he is now attending his school regularly. However, less improvement was observed reading his gait abnormality.
This case supports the current understanding regarding the persistent occurrence of HIV-associated neurocognitive disorder and HIV-associated myelopathy even decades after introduction of cART. Therefore, it's important to screen HIV+ patients for the HAND and HAM even if they have relatively preserved immunity. Because patient can be easily shifted to ART drugs with better CNS penetrating potential to achieve acceptable virological suppression level, to observe sound clinical improvement.
尽管广泛使用联合抗逆转录病毒疗法(cART),但 HIV 相关神经认知障碍(HAND)和 HIV 相关脊髓病(HAM)的发病率并没有显著降低。HAM 是一种进行性脊髓病,常在免疫抑制严重的患者中与 HAND 的严重形式同时发生。然而,在 cART 后时代,在相对保留 CD4 细胞的患者中,同时存在HAND 的较轻形式和 HAM 是一种罕见的临床实体。
我们报告了一名 16 岁男性,经垂直感染获得 HIV 感染,由于 3 年来病毒学失败,一直在接受二线治疗方案。他目前的 CD4 淋巴细胞计数为 835 个/μL,病毒 RNA 水平为 33008 拷贝/mL。目前表现为进行性健忘、步态失衡和频繁凝视发作,但姿势张力没有丧失。神经系统检查提示认知功能障碍,国际 HIV 痴呆量表评分为 6 分(运动速度=3,运动速度=2,记忆回忆=1)。下肢肌力为 4/5,腱反射亢进,步态不稳。脑 MRI 显示弥漫性皮质和白质 T2 和 FLAIR 高信号病变。胸椎 MRI 显示从中胸段到圆锥的异常 T2 信号延长。脑电图研究显示广泛严重的弥漫性减慢,双侧额颞叶区域有局灶性节律障碍的证据。血清维生素 B12 水平正常(286ng/mL)。考虑到病毒学失败、HAND、HAM 和癫痫发作,开始使用多替拉韦+拉米夫定+阿巴卡韦/利托那韦和丙戊酸钠治疗癫痫发作。在 6 个月的随访评估中,他的临床状况稳定,癫痫发作相关症状明显改善,认知功能障碍也有所改善,现在可以定期上学。然而,他的步态异常改善不明显。
该病例支持目前关于即使在引入 cART 几十年后,HIV 相关神经认知障碍和 HIV 相关脊髓病仍持续发生的认识。因此,即使患者免疫功能相对保留,也有必要对 HIV+患者进行 HAND 和 HAM 的筛查。因为患者可以很容易地转为具有更好中枢神经系统穿透能力的 ART 药物,以达到可接受的病毒学抑制水平,从而观察到良好的临床改善。