Cytomegalic inclusion body disease

Cytomegalic inclusion body disease (CIBD) also known as cytomegalic inclusion disease (CID) is a series of signs and symptoms caused by cytomegalovirus infection, toxoplasmosis or other rare infections such as herpes or rubella viruses. It can produce massive calcification of the central nervous system, and often the kidneys.[1]

Cytomegalic inclusion body disease
Differential diagnosiscytomegalovirus infection

Cytomegalic inclusion body disease is the most common cause of congenital abnormalities in the United States. It can also cause pneumonia and other diseases in immunocompromised patients, such as those with HIV/AIDS or recipients of organ transplants.[2]

Presentation

Various systems are affected.

  • CNS abnormalities – microcephaly, intellectual disability, spasticity, epilepsy, periventricular calcification
  • Eye – choroidoretinitis and optic atrophy
  • Ear – sensorineural deafness
  • Liver – hepatosplenomegaly and jaundice due to hepatitis
  • Lung – pneumonitis (interstitial pneumonitis)
  • Heart – myocarditis
  • Thrombocytopenic purpura, haemolytic anaemia
  • GI diseases in AIDS patients
  • Late sequelae in individuals asymptomatic at birth – hearing defects and reduced intelligence

The cells of the infected organ show intranuclear inclusion giving the nucleus classical owls eye appearance. Further tests like ELISA can be used to detect the antigen. Virus can be grown in cell culture also.

References
  1. Marquis JR, Lee JK (October 1976). "Extensive central nervous system calcification in a stillborn male infant due to cytomegalovirus infection". AJR. American Journal of Roentgenology. 127 (4): 665–7. doi:10.2214/ajr.127.4.665. PMID 184717.
  2. Levinson, Warren (2012). Review of Medical Microbiology and Immunology (12th ed.). McGraw-Hill. ISBN 978-0071774345.


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