Author
Information
(*
Second Year Resident, ** Professor, Department of Obstetrics &
Gynecology. Seth G.S.Medical College & KEM Hospital, Mumbai,
India.).
Abstract
We
are presenting a case where an
asymptomatic mother
infected with herpes, rubella and CMV virus
as diagnosed by elevated IgG
levels
of
all
these
three viruses gave
birth to a neonate
with microcephalus. On
serology,
titres of all these
three
viruses were found to be raised in the
neonate;
indicating that
the neonate
acquired infection in the
first
trimester
of the intrauterine life.
Introduction
TORCH
infection
is an acronym
for
infection caused by Toxoplasmosis,
Other (syphilis, varicella-zoster, parvovirus B19),
Hepatitis
B,
Rubella,
Cytomegalo and Herpes virus. This group of infections are a main
threat of serious congenital neonatal infection. Severity of
infection depends on the
gestational
age. In early pregnancy placenta forms a barrier that protects the
fetus from damage
caused by humoral
and cell mediated immunity response.[1]
Case
Report
A
22 year woman
married
since 6 year G2P1NND1L0 with moderate mitral stenosis of
rheumatic
etiology
with
non-immunized
Rh
negative status
registered
at our hospital at 6 months of amenorrhea. On antenatal
ultrasonography microcephalus with overriding of skull bone was
detected. On evaluation her TORCH serology
showed Herpesvirus1,
Cytomegalovirus and Rubella virus specific
IgG
titre values well above the
normal
range. IgG values for CMV was 65 IU/AU, for HSV1 was 150 IU/AU and
for Rubella was 135 IU/AU respectively. IgM
was negative. Her
other antenatal investigation profile was normal including HIV status
which was negative. Her blood group was O negative, her husband’s
blood group was A positive and her indirect coomb test (ICT) was
negative.
She had a
spontaneous term
delivery.
A
live female neonate with microcephalus
was born. There
were no other visible external anomalies detected at birth. The
neonate was further evaluated by neonatologist to find out the cause
of microcephalus. On imaging with MRI the brain showed diffused
cerebral and cerebellar hypoplasia, ventriculomegaly predominantly
involving lateral ventricles, gyral abnormality in both cerebral
hemispheres with paucity of gyri in left occipital region
representing Lisencephaly. Also there was periventricular
calcification of basal ganglia, frontal and parietal region. All
these features were suggestive of TORCH infection (most likely
because of CMV infection).
TORCH
titre of the
neonate
was positive for Cytomegolo virus, Rubella virus and Herpes virus
infection. Titre of IgG value for herpes virus 1and 2 was
29.90IU/ml(reactive >1.1), for Rubella was 78.21
IU/ml(reactive>10) and for CMV was 650.09 IU/ml(reactive>1.1)
respectively. The IgM antibodies were found negative in both, mother
and neonate for all three viruses indicating infection in earlier
trimester of pregnancy at least 3 month earlier than birth of child.
It was suspected that infection was because of CMV as titre of CMV
antibodies was much higher than other viruses antibodies titre.
Figure1.
Microcephalus.
Figure
2.
MRI
of brain.
The black hollow arrow shows the periventricular calcification.
For
further confirmation neonate’s urine sample was sent for DNA PCR,
which is a gold standard test for diagnosis of TORCH infection, which
came to be negative. Neonate was discharged on
oral
Gancycliovir 16mg/kg twice a day dose for six weeks and was
called
for further follow up after completion of the
dose.
Discussion
CMV
is a member of the herpesviridae family of viruses. The virus has a
property
of latency and reactivation.[1]
Symptomatic
infection occurs either in fetuses
or in patients with defective T-Cell immunity. CMV has property to
destroy host cell and disturb host defense
mechanism and persists as a latent infection in the host.[2]
Majority of the
infected
newborns remain asymptomatic other than those which are clinically
affected and the
immunosuppressed
ones.
CMV
is the
most
common congenital infection in the
new
born affecting 1%
of
all live births.[3]
Primary verses secondary infection during pregnancy is differentiated
on the basis of serologic testing. Presence of IgG and IgM antibodies
during pregnancy indicates primary infection
in a previous known seronegative woman.
The presence of maternal antibodies prior to conception along with
the presence of CMV virus by culture in new born confirms the
recurring infection in mother. A limited number of infants with
symptomatic congenital infections are known to have been born to
mother who were sero-positive before pregnancy.[4-6]
In
our case mother was totally asymptomatic except that she had a
previous unexplained neonatal death and her IgG titre
for CMV
was raised between
the two pregnancies. This shows
that the mother was infected before pregnancy and fetus got infected
which is a rare phenomena in case of primary CMV infection as
mother’s anti CMV antibodies prevents infection to the
fetus.
However in this pregnancy the fetus was probably affected because of
recurrent or
reactivation of the CMV infection.
Conclusion
Though
CMV infection is rare one, it is an important cause of microcephalus
in newborns affected. We need to follow up these babies with full
course of anti-viral treatment for their future
neuro-development.
References
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Pass R. Cytomegalovirus infection [published erratum in pediatr Rev 2002;13:0]. Pediatr Rev 2002;23:163-70.
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Noyola DE1, Demmler GJ, Nelson CT, Griesser C, Williamson WD, Atkins JT, Rozelle J,etal Early predictors of neurodevelopmental outcome in symptomatic congenital cytomegalovirus infection .J Pediatr 2001;138;325-31.
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Gaytant MA, Steegers EA, Semmekrot BA, Merkus HM, Galama JM. Congenital cytomegalovirus infection: review of the epidemiology and outcome. Obset Gynecol Surv 2002;57:245-56.
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Demmler GJ. Congenital cytomegalovirus infection and disease. Adv Pediatr Infect Dis 1996;11:135-62
Mehta
V, Gupta AS.
Microcephalus
In A Neonate Caused By Cytomegalo Virus (CMV)
JPGO 2015. Volume 2 No. 9. Available from: http://www.jpgo.org/2015/09/microcephalus-in-neonate-caused-by.html