Progressive rubella panencephalitis

Specialty| Infectious disease

Progressive rubella panencephalitis (PRP) is a neurological disorder which may occur in a child with congenital rubella.[1] It is a slow viral infection of the brain characterized by chronic encephalitis, usually manifesting between 8–19 years of age. It is believed to be due to a persistence or reactivation of rubella virus infection.[citation needed]

## Contents

* 1 Cause
* 2 Diagnosis
* 3 Treatment
* 4 Incidence
* 5 See also
* 6 References
* 7 Further reading

## Cause

It develops 6 months to 4 years after the primary rubella infection, which in most cases is a congenital rubella. In children with congenital rubella infection the deficits remain stable; neurological deterioration after the first few years of life is not believed to occur.[citation needed]

Progression of the disease can be divided into two stages:[citation needed]

* 1st stage: Behavioural Changes
* insidious onset
* subtle changes in behaviour and declining school work
* 2nd stage: Neurological Changes
* seizures – sometimes myoclonic
* cerebellar ataxia
* spastic weakness
* retinopathy, optic atrophy
* frank dementia leading to coma
* spasticity and brainstem involvement with death in 2–5 years

## Diagnosis

The diagnosis is considered when a child with congenital rubella develops progressive spasticity, ataxia, mental deterioration, and seizures. Testing involves at least CSF examination and serology. Elevated CSF total protein and globulin and elevated rubella antibody titers in CSF and serum occur. CT may show ventricular enlargement due to cerebellar atrophy and white matter disease. Brain biopsy may be necessary to exclude other causes of encephalitis or encephalopathy. Rubella virus cannot usually be recovered by viral culture or immunohistologic testing.[citation needed]

## Treatment

Although no specific treatment exists, the disease can be managed with anticonvulsants, physiotherapy, etc.[citation needed]

## Incidence

PRP is very rare and similar to SSPE but without intracellular inclusion bodies. Only 20 patients have been identified since first recognized in 1974.[citation needed]

## See also

* Subacute sclerosing panencephalitis

## References

1. ↑ Moore, David P. (2008) (in en). Textbook of clinical neuropsychiatry (2nd ed.). London: Hodder Arnold. p. 507. ISBN 9780340939536. https://books.google.com/books?id=7BKOLn3EpQsC&q=Progressive+rubella+panencephalitis&pg=PA507. Retrieved 6 August 2017.

## Further reading

* "Progressive rubella panencephalitis. Late onset after congenital rubella". N. Engl. J. Med. 292 (19): 990–3. 1975. doi:10.1056/NEJM197505082921902. PMID 1117960.
* "Rubella". Merck Manual. http://www.merck.com/mmpe/sec14/ch193/ch193e.html#sec14-ch193-ch193e-2804.
* Haukenes, G. (2002). "40. Slow viruses: Conventional Slow Virus Infections – Subacute Sclerosing Panencephalitis (SSPE)". in Haaheim, L. R.. A Practical Guide to Clinical Virology (2nd ed.). Wiley. ISBN 9780470844298. http://www3.interscience.wiley.com/cgi-bin/bookhome/103520508.

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