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- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- MedEspera: International Medical Congress for Students and Young Doctors
- MedEspera 2016
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/11037
Title: | Cytomegalovirus infections in children |
Authors: | Racovet, Angela |
Keywords: | CMV congenital infection;hepato-splenomegaly;intracranial calcifications;chorioretinitis |
Issue Date: | 2016 |
Publisher: | MedEspera |
Citation: | RACOVET, Angela. Cytomegalovirus infections in children. In: MedEspera: the 6th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2016, p.80-81. |
Abstract: | Introduction. Cytomegalovirus Infection (CMV) is one the most common congenital viral
infection and an important public health issue, which is widely spread in newborns, about 0.3% -
2.4%,characterized by symptomatic infection, clinical polymorphism, severe evolution and irreversible
sequelae (mental retardation, hepatitis and deafness), persistent viral infections Associated with risks of
reactivation of immunosuppressed states. The objective of the research is to study and highlight the
clinical and diagnostic peculiarities of CMV infection in infants and young children.
Materials and methods. A retrospective study was performed on a group of 42 children at ages
1month-3years, most of them (29 children-69%) aged under 12 months were from rural areas. Presenceof specific anti CMV IgM and IgG (ELISA test) in serum and CMV DNA in serum or urine by means
of PCR were confirmed in diagnosing CMV infection.
Results. The study results proved the presence of high risk perinatal factors for antenatal fetal
infection in over 53% of pregnant women: area of origin, low socioeconomic level, previous abortions
or mortality cases, infections during pregnancy, premature births in medical history. The current
gestation ended with premature birth in 10 (23%) cases, 12 cases of born at term infants (35.5%) showed
retarded intrauterine development. The clinical features of congenital CMV infection was multiformelike.
The reason for hospitalization was neurological, pulmonary and liver impairment. Neurological
examination revealed the presence of a neuro-psychological retardation of varying degrees in 21 (50%)
cases, periventricular calcifications in 10 (23.8%) children, microcephaly in 5 (12%) children. Liver
damage was characterized by hepatosplenomegaly and cytolisis in 2/3 of children. The ophthalmologic
examination revealed chorioretinitis in 5 (12%) children and optic nerve atrophy in 2 children. One child
was diagnosed with sensorineural deafness. Most children suffered from interstitial lung- pneumonia.
The disease diagnosis was confirmed by the presence of CMV-DNA in the serum of 7 children out of
11 investigations and DNA in the urine of 10 children out of 11 investigated ones. The serologic test
results were positive for CMV IgM antibodies in 23 (55%) cases and anti CMV IgG in 27 (64%) cases.
Conclusions. According to the survey, more than 53% of cases resulted from pathological
pregnancies. Interstitial pneumonia, hepatomegaly and cytolisis, periventricular calcification and
microcephaly, chorioretinitis and optic nerve atrophy were the most common clinical manifestations of
congenital CMV infection. The serologic positive results confirmed the diagnosis by presence of CMV
IgM and IgG antibodies and CMV DNA in serum or urine. |
URI: | http://repository.usmf.md/handle/20.500.12710/11037 |
ISBN: | 978-9975-3028-3-8. |
Appears in Collections: | MedEspera 2016
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