Cytomegalovirus Infection
Also called generalized salivary gland disease and cytomegalic inclusion disease, cytomegalovirus (CMV) occurs worldwide. A herpesvirus, the disease is transmitted by human contact. Most CMV infections are asymptomatic and the virus remains latent.
In most, the disease is so mild that it’s overlooked. However, CMV can be devastating to a fetus or to an immunosuppressed patient.
Causes
The infection results from the cytomegalovirus, an ether-sensitive, deoxyribonucleic acid virus belonging to the herpes family. CMV has been found in the saliva, urine, semen, breast milk, feces, blood, and vaginal and cervical secretions of infected people.
Transmission occurs through direct contact with secretions and excretions, through blood transfusions, through the placenta, and through transplanted organs (patients who receive organs from a CMV-seropositive donor run a 90% chance of contracting the infection). CMV in cervical secretions can infect a sexual partner or an infant during passage through the birth canal. CMV is reaching epidemic proportions in female prostitutes and sexually active homosexual
males as CMV antibody titers in these groups approach 100%.
males as CMV antibody titers in these groups approach 100%.
The disease probably spreads through the body in lymphocytes or mononuclear cells to the lungs, liver, GI tract, eyes, and central nervous system, where it often produces inflammatory reactions.
Complications
Immunosuppressed patients, such as those with acquired immunodeficiency syndrome, may develop opportunistic infections, such as pneumonia, hepatitis, ulceration of the GI tract, retinitis, and encephalopathy.
Pediatric pointer
Congenital CMV can lead to neonatal retinitis, microcephaly, mental retardation, seizures and, later, hearing loss. The infant can also develop thrombocytopenia and hemolytic anemia. Stillbirth is also possible.
Assessment
There are predominantly three clinical syndromes for CMV: acute acquired CMV infection, CMV in immunocompromised hosts, and perinatal. The adult patient’s history may reveal an immunosuppressive condition. He may complain of mild, nonspecific clinical symptoms, such as fatigue, myalgia, and headache, or he may have no symptoms.