HIV-associated neurocognitive disorders
HIV-associated neurocognitive disorders (HANDs), is a term that emerged from an international conference in 2006 1, and corresponds to a group of clinical syndromes related to the HIV infection in the cells of the nervous system expressing different degrees of impairment of cognition and associated functioning. They are part of neuroAIDS.
Three different clinical conditions have been defined 1-3:
- asymptomatic neurocognitive impairment: characterized by impairment in cognitive function clinically diagnosed, however the everyday functioning is not affected
- mild neurocognitive disorder: characterized by impairment in cognitive function clinically diagnosed and mild interference in everyday functioning
- HIV-associated dementia (HAD): characterized by marked impairment in cognitive function which significantly limits abilities to function in daily work, home and social activities. It was previously referred as AIDS dementia complex and is the only condition which demonstrates clear recognisable features of HIV encephalopathy on MRI.
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Infections of the central nervous system
-
CNS infections
- classification by etiology
- viral
- bacterial
- CNS listeriosis (Listeria monocytogenes)
- CNS nocardiosis (Nocardia spp)
- CNS tuberculosis (Mycobacterium tuberculosis)
- Lyme disease (Borrelia burgdorferi)
- neurobrucellosis (Brucella sp.)
- neurosyphilis (Treponema pallidum)
- Rocky Mountain spotted fever (Rickettsia rickettsii)
- fungal
- CNS aspergillosis (Aspergillus spp)
- CNS coccidioidomycosis (Coccidioides immitis)
- CNS cryptococcosis (Cryptococcus neoformans)
- CNS mucormycosis (order Mucorales)
- neurocandidiasis (Candida spp)
- parasitic
- cerebral amoebiasis
- primary amoebic meningoencephalitis (Naegleria fowleri)
- granulomatous amoebic encephalitis (Acanthamoeba spp, Balamuthia mandrillaris and Sappinia pedata)
- cerebral malaria (Plasmodium falciparum)
- cerebral sparganosis (Spirometra mansonoides)
- neurocysticercosis (Taenia solium)
- neurohydatidosis (Echinococcus spp)
- neurotoxoplasmosis (Toxoplasma gondii)
- neuroschistosomiasis
- cerebral amoebiasis
-
prion
- Creutzfeldt-Jakob disease (sporadic, variant, familial, and iatrogenic)
- fatal familial insomnia
- Gerstmann-Straussler-Scheinker disease
- kuru
- variably protease-sensitive prionopathy
- others or those with possible infectious etiologies
- acute necrotizing encephalopathy of childhood
- encephalitis lethargica
- hemorrhagic shock and encephalopathy syndrome
- Mollaret meningitis (idiopathic recurrent meningitis)
- Rasmussen encephalitis
- classification by location
- extra-axial
- intra-axial
- classification by etiology