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ultrasound diagnosis of fatal anomalies

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INFECTIONS

Congenital Varicella

Definition: Infection with varicella zoster virus.

This is a DNA virus belonging to the family of

herpesviruses. The primary infection causes

chickenpox; reactivation of the virus at a later

stage from the sensory roots of the posterior

horn of the spinal cord is responsible for the

clinical symptoms of herpes zoster.

Incidence: Maternal infection during pregnancy,

one in 2000–10 000. The risk of congenital infection

to the fetus is low; congenital malformations

result in less than 5% of cases.

Origin: The virus affects the nervous system,

causing neurological impairment of fetal structures.

Infections in the first trimester cause the

most severe damage.

Clinical features: Focal ulceration of the skin and

anomalies described in the following section.

Ultrasound findings: Rarely, the following are

detected: growth restriction, hydramnios, microphthalmia,

hydrocephalus, or microcephaly;

ascites, pleural effusions and even full-fledged

fetal hydrops; hepatic calcification, club feet and

other limb anomalies, reduction in fetal movements.

These anomalies develop only in the

most severely affected cases, about 3–12 weeks

after maternal infection.

Clinical management: Serology of maternal

blood; fetal IgM is detectable from 20 weeks,

amniotic fluid culture, chorionic villus sampling

and polymerase chain reaction, regular scanning

controls (is hydrocephalus developing?). IgG

may be given to the mother within 72–96 h if the

mother has been in contact with an infected individual

and is not immune.

Procedure after birth: Acyclovir may be given

after birth.

Prognosis: The infants usually do not show any

symptoms. Fetal anomalies appear in 1–2% of

cases if infection occurs before 20 weeks of gestation.

About one-third of the most severely affected

infants die in the early neonatal stage; in

the surviving infants, mental impairment and

fits may occur.

References

Dufour P, de Bièvre P, Vinatier D, et al. Varicella and

pregnancy. Eur J Obstet Gynecol Reprod Biol 1996;

66: 119–23.

Harger JH, Ernest JM, Thurnau GR, et al. Frequency of

congenital varicella syndrome in a prospective cohort

of 347 pregnant women. Obstet Gynecol 2002;

100: 260–5.

Kerkering KW. Abnormal cry and intracranial calcifications:

clues to the diagnosis of fetal varicella-zoster

syndrome [review]. J Perinatol 2001; 21: 131–5.

Lecuru F, Taurelle R, Bernard JP, et al. Varicella zoster

virus infection during pregnancy: the limits of prenatal

diagnosis. Eur J Obstet Gynecol Reprod Biol

1994; 56: 67–8.

Mets MB. Eye manifestations of intrauterine infections

[review]. Ophthalmol Clin North Am 2001; 14: 521–

31.

Petignat P, Vial Y, Laurini R, Hohlfeld P. Fetal varicellaherpes

zoster syndrome in early pregnancy: ultrasonographic

and morphological correlation. Prenat

Diagn 2001; 21: 121–4.

Pons JC, Vial P, Rozenberg F, et al. Prenatal diagnosis of

fetal varicella in the second trimester of pregnancy. J

Gynecol Obstet Biol Reprod (Paris) 1995; 24: 829–38.

Taylor WG, Walkinshaw SA, Thomson MA. Antenatal

assessment of neurological impairment. Arch Dis

Child 1993; 68: 604–5.

Yaron Y, Hassan S, Geva E, Kupferminc MJ, Yavetz H,

Evans MI. Evaluation of fetal echogenic bowel in the

second trimester. Fetal Diagn Ther 1999; 14: 176–80.

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