HIV-associated neurocognitive disorder and HIV-associated myelopathy in a patient with a preserved CD4, but high viral load-a rarely reported phenomenon: a case report and literature review

被引:7
作者
Ayele, Biniyam Alemayehu [1 ]
Amogne, Wondwossen [2 ]
Gemechu, Lalise [2 ]
机构
[1] Addis Ababa Univ, Coll Hlth Sci, Dept Neurol, POB 6396, Addis Ababa, Ethiopia
[2] Addis Ababa Univ, Coll Hlth Sci, Dept Internal Med, Addis Ababa, Ethiopia
关键词
HIV-associated neurocognitive disorder; Seizure; cART; HIV-associated myelopathy; VACUOLAR MYELOPATHY; PARAPLEGIA; AFRICA; ADULTS; AIDS;
D O I
10.1186/s12879-020-05297-9
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
BackgroundDespite 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.Case presentationWe report a 16-year old male, acquired HIV infection vertically, was on second line regimen because of virological failure since 3years. 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 (286ng/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.ConclusionThis 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.
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