Cytomegalovirus (CMV) encephalitis is a CNS infection that almost always develops in the context of profound immunosuppression.
This article focus on adult infection. CMV is also one of the most frequent prenatal infections, which is discussed separately: congenital CMV infection.
It is extremely rare to involve immunocompetent individuals.
Presentation is variable, however generalized cognitive decline is most frequent. Focal neurological signs and cranial nerve palsies are uncommon to rare.
At autopsy active CMV infection is also seen systemically although clinical manifestations are variable:
- CMV adrenalitis (92%)
- CMV pneumonitis (42%)
- CMV retinitis (58%)
Typically, before CMV infections become clinically apparent the patient's CD4+ count typically reaches below 50/mm3 2. CMV infects the entire neuraxis (brain, spinal cord, meninges, nerve roots, eye) and therefore has variable presentation.
Cytomegalovirus is a DNA virus belonging to the herpesviruses group, and is also known as Human Herpesvirus 5 (HHV-5). It is found in all geographic locations and socioeconomic groups, and infects between 50-80% of adults in the United States as indicated by the presence of antibodies in much of the general population.
Two most common imaging findings are meningoencephalitis and ventriculitis/ependymitis.
In CMV encephalitis, there is usually only non specific increased T2/FLAIR signal in the white matter. If ventriculitis is also present then enhancement of the ependymal surface and hydrocephalus may also be seen.
high T2 white matter change most prominent in a periventricular distribution
- no enhancement (unless ventriculitis present, in which case 30% or so will enhance)
- no mass effect (often seen with concurrent atrophy)
Appearances are similar to HIV encephalitis, although usually CMV occurs in patients with a longer duration of disease, and lower CD4+ counts.
Other white matter changes in HIV, especially :
- HIV encephalitis
- progressive multifocal leukoencephalitis (PML)
- primary CNS lymphoma: periventricular but has mass effect and enhances
Particularly in a profoundly immunocompromised patient, ventriculitis characterized by high T2/FLAIR signal and post contrast enhancement is highly suggestive of CMV infection.
- 1. Holland NR, Power C, Mathews VP et-al. Cytomegalovirus encephalitis in acquired immunodeficiency syndrome (AIDS). Neurology. 1994;44 (3): 507-14. Pubmed citation
- 2. HIV-1 Associated Opportunistic Infections - Cytomegalovirus Encephalitis by Niranjan N Singh from emedicine.com. HIV-1 Associated Opportunistic Infections - Cytomegalovirus Encephalitis
- 3. Ketonen L, Hiwatashi A, Sidhu R. Pediatric brain and spine, an atlas of MRI and spectroscopy. Springer Verlag. (2005) ISBN:3540213406. Read it at Google Books - Find it at Amazon
- 4. Kleinschmidt-DeMasters BK, Miravalle A, Schowinsky J et-al. Update on PML and PML-IRIS occurring in multiple sclerosis patients treated with natalizumab. J. Neuropathol. Exp. Neurol. 2012;71 (7): 604-17. doi:10.1097/NEN.0b013e31825caf2c - Pubmed citation
- 5 . Smith A, Smirniotopoulos J, Rushing E. Central Nervous System Infections Associated with Human Immunodeficiency Virus Infection: Radiologic-Pathologic Correlation1. Radiographics. 2008;28 (7): 2033-2058. Radiographics (full text) - doi:10.1148/rg.287085135
Related Radiopaedia articles
Infections of the central nervous system
- classification by etiology
- Eastern equine encephalitis
- enterovirus rhombencephalitis
- flavivirus encephalitis
herpes virus family
- herpes simplex virus 1 (HSV-1) encephalitis
- herpes simplex virus 2 (HSV-2) encephalitis
- varicella zoster virus (VZV) encephalitis
- Epstein-Barr virus (EBV) encephalitis
- cytomegalovirus (CMV) encephalitis
- human herpesvirus 6 (HHV-6) encephalitis
- HIV CNS manifestations
- HTLV-1-associated myelopathy
- JC virus
- measles encephalitis
- Nipah virus (NiV) encephalitis
- rabies encephalitis
- 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)
- cerebral amoebiasis
- cerebral malaria (Plasmodium falciparum)
- cerebral sparganosis (Spirometra mansonoides)
- neurocysticercosis (Taenia solium)
- neurohydatidosis (Echinococcus spp)
- neurotoxoplasmosis (Toxoplasma gondii)
- Creutzfeldt-Jakob disease (sporadic, variant, familial, and iatrogenic)
- fatal familial insomnia
- Gerstmann-Straussler-Scheinker disease
- variably protease sensitive prionopathy
- others or those with possible infectious etiologies
- classification by location
- classification by etiology