Neuropediatrics 2020; 51(03): 221-224
DOI: 10.1055/s-0039-3402011
Short Communication
Georg Thieme Verlag KG Stuttgart · New York

Neonatal Herpes Simplex Virus-1 Recurrence with Central Nervous System Disease in Twins after Completion of a Six-Month Course of Suppressive Therapy: Case Report

Anthony Grondin
1   Neonatal Unit, Department of Paediatrics, CHU of Reunion Island, Northern Hospital Group, Saint-Denis, France
,
Eloïse Baudou
2   Neurology Unit, Department of Paediatrics, CHU of Toulouse Purpan, Toulouse, France
,
Marlène Pasquet
3   Immunology Unit, Department of Paediatrics, CHU of Toulouse Purpan, Toulouse, France
,
Sonia Pelluau
4   Pediatric Intensive Care, Department of Paediatrics, CHU of Toulouse Purpan, Toulouse, France
,
Karim Jamal-Bey
5   Cardiology Unit, Department of Paediatrics, CHU of Reunion Island, Southern Hospital Group, Réunion, France
,
Cécile Bermot
6   Department of Radiology, Georges POMPIDOU Hospital, Paris, France
,
Frederic Villega
7   Neurology Unit, Department of Paediatrics, CHU of Bordeaux, Aquitaine, France
,
Emmanuel Cheuret
8   Neurology Unit, Department of Paediatrics, CHU of Toulouse Purpan, Toulouse, France
› Author Affiliations
Further Information

Publication History

20 June 2019

06 November 2019

Publication Date:
30 December 2019 (online)

Abstract

Seventeen-day-old twins were hospitalized for neonatal herpes simplex virus 1 (HSV-1) with central nervous system disease and internal capsule and thalamic lesions on magnetic resonance imaging (MRI). They were treated with the usual intravenous (IV) treatment and oral therapy for 6 months. The clinical course was good in both children with negative HSV polymerase chain reaction on completion of IV therapy. The neurological condition recurred in one child with new radiological lesions at 7 months of age, 2 weeks after discontinuation of oral treatment. Cerebral lesions highlighted on the MRI scan are specific to the neonatal period and impact long-term prognosis. The likely genetic predisposition in this case is interesting and requires further investigation. In addition, this case raises questions about the duration of oral acyclovir suppressive therapy.

 
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