Book of Medical Disorders in Pregnancy - Tintash
Book of Medical Disorders in Pregnancy - Tintash
Book of Medical Disorders in Pregnancy - Tintash
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identify<strong>in</strong>g a primary <strong>in</strong>fection<br />
accurately.<br />
Immunity: Infection with CMV confers<br />
immunity <strong>in</strong> the host because persistence<br />
<strong>of</strong> the agent <strong>in</strong> a latent phase and<br />
reactivation <strong>in</strong> response to various<br />
stimuli occurs. Although unusual, a<br />
woman may bear a second child with<br />
congenital <strong>in</strong>fection <strong>of</strong> the same serotype.<br />
S<strong>in</strong>ce cytomegalovirus exists <strong>in</strong><br />
multiple serotypes, re<strong>in</strong>fection <strong>of</strong> a<br />
woman <strong>in</strong> the childbear<strong>in</strong>g age with a<br />
different type can result, <strong>in</strong> the birth <strong>of</strong><br />
another <strong>in</strong>fected <strong>in</strong>fant to the same<br />
mother. These occurrences nevertheless<br />
are very rare. In general after the birth <strong>of</strong><br />
a congenitally <strong>in</strong>fected <strong>in</strong>fant the fetus <strong>in</strong><br />
the subsequent pregnancy is not at<br />
significantly greater risk.<br />
Fetal <strong>in</strong>fection: Intrauter<strong>in</strong>e <strong>in</strong>fection<br />
with CMV is probably the most common<br />
viral <strong>in</strong>fection <strong>of</strong> the human fetus. It has<br />
been estimated that the prevalence <strong>of</strong><br />
CMV <strong>in</strong>fection at birth shows a<br />
frequency <strong>of</strong> 4 to 10 <strong>in</strong>fected <strong>in</strong>fants per<br />
1,000 births. Many po<strong>in</strong>ts <strong>of</strong> similarity<br />
can be found between congenital CMV<br />
and Rubella, but <strong>in</strong> general there is a<br />
lower frequency <strong>of</strong> congenital disease <strong>in</strong><br />
CMV with a preponderance <strong>of</strong> damage<br />
to the CNS <strong>in</strong> contrast to the<br />
comb<strong>in</strong>ation <strong>of</strong> malfor-mation and<br />
congenital disease which is to be found<br />
<strong>in</strong> <strong>in</strong>fants with congenital Rubella.<br />
Another common feature is that the<br />
<strong>in</strong>fant may be excret<strong>in</strong>g virus at birth yet<br />
show no symptoms. The majority rema<strong>in</strong><br />
unaffected as they grow older.<br />
Approximately one <strong>in</strong> 10 <strong>of</strong> congenitally<br />
<strong>in</strong>fected <strong>in</strong>fant develops symptoms. The<br />
fulm<strong>in</strong>at<strong>in</strong>g illness may present with<br />
hepatosplenomegaly, jaundice, petechial<br />
rash and low birthweight. The <strong>in</strong>fant<br />
may also be premature. The mortality<br />
168<br />
rate is high, particularly if CNS<br />
<strong>in</strong>volvement is prom<strong>in</strong>ent or respiratory<br />
distress is present. The prognosis for<br />
<strong>in</strong>fants with jaundice and thrombocytopenic<br />
purpura alone is better than for<br />
those who have CNS <strong>in</strong>volvement. In<br />
many <strong>in</strong>fants with the former symptoms<br />
recovery is complete <strong>in</strong> 6 to 8 weeks, but<br />
there is always the possibility that other<br />
symptoms may develop later. The<br />
neurological symptoms are <strong>of</strong> the<br />
greatest consequence both <strong>in</strong> the short<br />
terms and long terms. Microcephaly may<br />
be obvious at birth or become apparent<br />
later <strong>in</strong> <strong>in</strong>fancy. Cerebral diplegia,<br />
spasticity and fits present<strong>in</strong>g early <strong>in</strong> life<br />
usually have a bad prognosis. Henshaw<br />
et al (1973) found a higher <strong>in</strong>cidence <strong>of</strong><br />
CMV <strong>in</strong>fection determ<strong>in</strong>ed by the presence<br />
<strong>of</strong> CF antibody <strong>in</strong> children with<br />
undiagnosed seizures and microcephaly<br />
than <strong>in</strong> patients with genetically determ<strong>in</strong>ed<br />
CNS disease and <strong>in</strong> a control<br />
group <strong>of</strong> normal children.<br />
Fig13.3: shows CMV <strong>in</strong>fection rash on<br />
the body<br />
Toxoplasmosis: Toxoplasma gondii is a<br />
parasite which has a proliferative<br />
(<strong>in</strong>vasive) phase and a cystic (resistant)<br />
phase. The resistant phase is formed <strong>in</strong><br />
response to the immune reaction <strong>of</strong> the<br />
host. The mode <strong>of</strong> <strong>in</strong>fection is unknown.<br />
The <strong>in</strong>fection occurs <strong>in</strong> most parts <strong>of</strong> the<br />
world but is particularly prevalent <strong>in</strong><br />
warm and humid climates.