Indian Journal of Dermatology, Venereology and Leprology Medknow Publications on behalf of The Indian Association of Dermatologists, Venereologists and Leprologists (IADVL) ISSN: 0378-6323 EISSN: 0973-3922 Vol. 76, Num. 6, 2010, pp. 724-724

Indian Journal of Dermatology, Venereology, and Leprology, Vol. 76, No. 6, November-December, 2010, pp. 724

Net Case

Fetal varicella syndrome

S Ramachandra, Arun Kumar Metta, Nayeem Sadath Haneef, Sandeep Kodali

Department of Dermatology, Venereology and Leprology, Kamineni Institute of Medical Sciences, Narketpally, Nalgonda, Andhra Pradesh, India

Correspondence Address: S Ramachandra Professor and Head, Department of DVL, Kamineni Institute of Medical Sciences, Narketpally, Nalgonda, Andhra Pradesh India dr_sramoo@yahoo.co.in

Code Number: dv10222

DOI: 10.4103/0378-6323.72475

Abstract

Keywords: Fetal varicella syndrome, congenital varicella syndrome, congenital varicella zoster syndrome

Introduction

Fetal varicella syndrome (FVS) is a rare complication of maternal varicella infection occurring in <2% of the babies born to women infected with varicella between 7 and 28 weeks of pregnancy. ^[1],[2],[3] The newborn may present with low birth weight, cutaneous scars, papular lesions, localized absence of skin on a limb, hypoplasia of one or more limbs, malformed digits along with various ocular and central nervous system (CNS) abnormalities. ^[3],[4] We are reporting one such case in view of paucity of reports from the Indian subcontinent. ^[5]

Case Report

Dermatologists opinion was sought for a newborn male baby on the 2 ^nd day of birth, born with scars over the left upper limb. There was no history of vesiculobullous lesions. The baby was born to a 22-year-old lady (gravida 2 para 1) at full term by cesarian delivery for non-progression of labor. She had a history of chicken pox during the first trimester of pregnancy. Birth weight of the child was 3.2 kg and APGAR score was 8-10. There was no history of consanguinity. Investigations like ultrasonography (fetal anomaly scan) or TORCH battery could not be performed as the mother did not get routine antenatal check ups in our hospital. The previous delivery was a full-term normal vaginal delivery and the baby was healthy.

Cutaneous examination of the child revealed a linear, irregular, depressed, erythematous scar measuring 12 cm × 5 cm over the anteromedial aspect of the left forearm. A similar small scar was present over the left axillary fold [Figure - 1] and [Figure - 2]. This distribution corresponds to C8 and T1 dermatomes. There was no limb hypoplasia, malformed digits, ocular changes or CNS abnormalities. There were no skeletal deformities on X-ray. The patient's routine blood and urine parameters were within normal limits. His blood group was O positive and Venereal Diseases Research Laboratory test and human immunodeficiency virus antibodies were non-reactive. Differential diagnosis of neonatal scars was considered [Table - 1], but a diagnosis of FVS was made based on the characteristic history and clinical features.

The parents of the baby were counseled about the condition and reassured. No active intervention was advised at this stage.

Discussion

Chicken pox may develop during pregnancy in one to five per 10,000 pregnancies. If infection occurs during the last 2 weeks of pregnancy, the infection may be transmitted to the fetus and the newborn may present with varicella at or soon after birth. ^[2] The neonate may develop severe disseminated varicella and septicemia with increased mortality (up to 28%) if maternal infection occurs 5 days before or after delivery due to the absence of protective maternal antibodies. ^[2] Occasionally, herpes zoster can occur in early infancy if the child has been infected with varicella zoster virus during early intrauterine life. ^[6] Maternal varicella occurring between 7 and 28 weeks of pregnancy may lead to either spontaneous abortions or "fetal varicella syndrome" [Table - 2]. ^{[2],[4],[5],[6]}

FVS was first described in 1947 by La Foret and Lynch. ^[1] Srabstein et al. rediscovered the syndrome in 1974 and named it "congenital varicella syndrome." ^[7],[8] Subsequently, the condition has been reported under various names like congenital varicella zoster syndrome, fetal varicella zoster syndrome, varicella embryopathy, varicella embryofetopathy, etc.

A majority of the cases (90%) of FVS occur as a complication due to maternal varicella infection during the 1 ^st or 2 ^nd trimesters of pregnancy, and a few cases (10%) follow maternal herpes zoster. ^[7] Risk of transmission to fetus is approximately 2% and is especially more common when the mother has infection between the 13 ^th and 20 ^th weeks of gestation. ^[3],[6]

The typical clinical features include low birth weight, cutaneous lesions like scars often in a dermatomal outline (70%), papular lesions resembling connective tissue nevi, ocular abnormalities (66%) like choreoretinitis, cataracts, microophthalmia, Horner's syndrome, nystagmus, limb hypoplasia (50%), CNS abnormalities (46%) including seizures, mental retardation, hydrocephalus, cortical atrophy, cerebellar aplasia, encephalomyelitis and dorsal radiculitis, and poor sphincter control (32%). ^[7]

In anticipated cases of FVS, amniocentesis, fetal blood and chorionic villous sampling may be performed to isolate the virus or to detect specific IgM. Pregnant women who are suspected not to be immune and who experience exposure to varicella zoster should be given varicella zoster immunoglobulin (VZIG) within 3 days after contact, although the efficacy is doubtful. ^[2] Termination of pregnancy is not indicated as the risk of fetal damage is less. Plastic surgery may be considered for the scars and limb abnormalities.

The case described above shows cutaneous scars typical of FVS, and there is history of varicella in the mother during the first trimester of pregnancy. The segmental distribution of scars probably reflects damage to the fetal nervous system by the neurotrophic virus. ^[8],[9] Our case is being reported to increase awareness about this rare but fascinating condition, which requires a high index of suspicion and careful history for diagnosis.

References

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