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CNS infection in HIV patients
Int.Naruenont Dolsaritchaiya th June 2013
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Outline Approach Common diseases - basic knowledges
- medical treatment - surgical indication Take home messages
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How to approach HIV patients can acquire both opportunistic infections and others found in normal host Work up should be extensive due to the possibility of multiple infections However, opportunistic infection should draw attention firstly
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How to approach Algorithm
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How to approach Source : HIV-associated Opportunistic
infections of the CNS Lancet Neurol 2012; 11:
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How to approach Lesions can be categorized into 3 types based on radiological appearance : 1.Focal mass 2.White matter disease 3.Meningeal disease
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How to approach Focal masses Focal masses with rim-enhancement
1.Toxoplasmosis 2.Tuberculoma 3.Cryptococcoma 4.Primary CNS lymphoma (not infection) 5.Bacterial and fungal abscesses 6.CMV encephalitis (rarely)
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How to approach Focal masses Focal masses without rim-enhancement
1.Toxoplasmosis 2.Cryptococcoma 3.Atypical primary CNS lymphoma
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How to approach White matter disease 1.HIV encephalopathy (HIVE)
2.CMV encephalitis 3.Progressive multifocal leukoencephalopathy (PML)
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How to approach Meningeal disease 1.HIV meningoencephalitis
2.Cryptococcal meningitis 3.Tuberculous meningitis 4.Other bacterial/viral meningitis
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Common diseases
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Toxoplasmosis Principal OI in HIV patients 15-40% of AIDS patients
Usually occurs when CD4 < 100 Almost always a reactivation and serology is positive in 85% Seronegative cases occur as a result immunosuppression or rarely a primary infection
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Toxoplasmosis Common sites : 1.Basal ganglia
2.Cortico-medullary junction usually frontal and parietal lobe 3.Brainstem Meningeal involvement uncommon
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Toxoplasmosis Diagnosis 1. Imaging : CT/MRI - rim-enhancing lesion
- typically 1-2 cm - < 20% solitary 2.Serology : IgG, IgM 3.PCR
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Toxoplasmosis
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Toxoplasmosis Treatment : Pyrimethamine + Sulfadiazine 6 weeks
In cases of failure to diagnose or respond to medical treatment within 7 days, biopsy is needed for tissue pathological diagnosis Secondary prophylaxis until CD4 > 200 for 6 months
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Tuberculosis Found in both immunocompromised and immunocompetent host
HIV patients are prone to develop reactivation and extrapulmonary infection Tuberculous meningitis and tuberculoma/TB abscess (uncommon)
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Tuberculosis CN III palsy
Involves cerebral artery which can produce focal ischemia
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Tuberculosis Diagnosis 1.CSF profile : mainstay for Dx
***AFB +ve in 1/3 2.Imaging : CT/MRI
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Tuberculosis Diagnosis : CSF profile
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Tuberculosis Imaging : CT/MRI
- Leptomeningeal enhancement mainly at the base of skull - tuberculoma at basal ganglia - communicating/noncommunicating hydrocephalus
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Tuberculosis Imaging : CT/MRI
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Tuberculosis Treatment : HRZE x 9 months or more
***Steroid reduces morbidity In case of hydrocephalus, extraventricular drainage or shunt is required to reduce ICP
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Cryptococcosis Usually develops when CD4 < 100
Forms : meningitis/cryptococcoma pulmonary skin and soft tissue Meningismus may be absent Complication : CN deficit, visual loss, cognitive impairment
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Cryptococcosis Poor prognosis : - +ve Indian ink - high CSF pressure
- low glucose - low pleocytosis < 2 cells/mm3 - extraneural yeast cell - absence of Ab - CSF or serum crypto. Ag > 1:32 - steroid use - hematologic malignacy
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Cryptococcosis Diagnosis 1.Indian ink 2.Cryptococcal Ag in CSF/serum
3.Imaging : CT/MRI
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Cryptococcosis
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Cryptococcosis Imaging : CT/MRI - hydrocephalus
- meningeal enhancement - cryptococcomas at basal ganglion - punched-out cystic lesion
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Cryptococcosis Imaging : CT/MRI
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Cryptococcosis Treatment :
Amp. B mg/kg/day 2 weeks and then fluconazole 400 mg/day for 10 weeks Repeated LP or shunt is necessary to relieve increased ICP Secondary prophylaxis until CD4 > 200 for 6 months
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Primary CNS lymphoma Frequently occurs in severe immunosuppression or AIDS High grade B-cell lymphoma Strongly associated with EBV Poor prognosis compared to similar lymphoma outside CNS
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Primary CNS lymphoma Imaging : CT/MRI
- rim-enhancing or heterogeneously enhancing - usually > 3 cm - periventricular, frontal, temporal Difficult to distinguish from toxoplasmosis or metastasis
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Primary CNS lymphoma Diagnosis usually made after failure to respond to toxoplasmosis Rx Brain biopsy is mandatory to obtain tissue pathology If safe to LP, CSF for EBV DNA help to diagnose with no need to perform biopsy
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Primary CNS lymphoma Imaging : CT/MRI
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Primary CNS lymphoma Treatment : CMT + WBRT
> 90% have a recurrence disease Surgical resection : for immediate decompresion of life-threatening mass effect
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HIV encephalopathy HIV-associated dementia
Symptoms : progressive dementia, cognitive impairment, motor symptoms, gait disturbance, tremor Subcortical dementia : no aphasia, apraxia or agnosia Alertness is minimally perturbed
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HIV encephalopathy Diagnosis 1.Imaging : CT/MRI 2.CSF profile
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HIV encephalopathy Imaging : CT/MRI
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HIV encephalopathy CSF profile
- non specific increased in cells and protein - helpful in diagnosing or ruling out OI - HIV RNA not correlate with HIV encephalopathy
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HIV encephalopathy Treatment : HAART CNS resistance may occur
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CMV encephalitis Usually occurs when CD4 < 50
Reactivation of latent infection Two forms : 1.Encephalitis : progressive dementia 2.Ventriculoencephalitis : CN deficit, alteration of consciousness, nystagmus, disorientation, ventriculomegaly
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CMV encephalitis Diagnosis 1.CSF : PCR for CMV DNA culture
2.Imaging : CT/MRI - periventricular enhancement ***no calcification like congenital CMV - subependymal enhancement - 50% normal imaging
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CMV encephalitis Imaging : CT/MRI
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CMV encephalitis Treatment : Ganciclovir, Valganciclovir
induction of days followed by prolonged maintenance therapy Secondary prophylaxis until CD4 > 100 for 3 months
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PML Caused by the reactivation of the Jamestown Canyon (JC) virus
CD4 counts usually below 100/mm3 Multiple areas of demyelination throughout the brain sparing cord and optic nerve
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PML Symptoms : visual loss mental impairment weakness ataxia
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PML Diagnosis : 1. MRI - multifocal asymmetric white matter lesions
- subcortical white matter, cerebellum - low signal on T1 weighted images and hyperintense on T2 weighted/FLAIR
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PML Diagnosis : MRI
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PML Diagnosis : 2.CSF : PCR for JCV DNA normal cells and protein
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HSV encephalitis HSV produces necrotizing encephalitis in HIV patients
Predilection for the medial temporal and inferior frontal lobes
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HSV encephalitis Diagnosis : 1.CSF : PCR for HSV DNA
- sens. 96% and spec. 99% (equivalent or exceed brain biopsy) - maybe negative if too early (< 72 hr) or more than 14 days
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HSV encephalitis Diagnosis : 2.Imaging : CT/MRI
- area of low absorption, mass effect or hemorrhage on CT - hyperintensity signal on T2/FLAIR or diffuse-weighted
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HSV encephalitis Imaging : CT/MRI
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HSV encephalitis Treatment : IV acyclovir 10 mg/kg q 8 hr for 14 days and repeat CSF profile *** Dilute < 7mg/ml and infused slowly over 1 hr to minimize renal dysfunction
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Take home messages Neurological manifestations in HIV/AIDS patients have a wide spectrum Clinicians must consider multiple causes which share similar clinical and radiographic patterns Neurosurgery carry an important role for diagnosis and treatment
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References Youman textbook of neurosurgery 6th ed.
Harrison textbook of internal medicine 17th ed. Lancet neurology 2012
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THANK YOU
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