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MINI REVIEW article
Front. Pediatr.
Sec. Pediatric Immunology
Volume 13 - 2025 | doi: 10.3389/fped.2025.1561339
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Herpes Zoster (HZ), caused by reactivation of varicella zoster virus (VZV), is an uncommon cause of rash in pediatrics, which can lead to concerns of an underlying immunodeficiency. We reviewed studies on HZ in children. Diagnosis of HZ can usually be established based on the clinical and epidemiological features. HZ is associated with T-cell immune defects that can be secondary to infections with HIV, tuberculosis and other pathogens, diabetes, malnutrition and cancer, or to primary immunodeficiency. Important clinical clues indicating that HZ is due to an underlying immunodeficiency include recurrent HZ during a short period, disseminated HZ, new lesions more than a week after presentation, prolonged course despite antiviral medications, a history of recurrent, invasive, or prolonged infections by other pathogens and a family history of an immunodeficiency or consanguinity. Reassuring features include exposure to VZV prior to one year of age or a compromised or incomplete VZV vaccination schedule. Initial laboratory analysis could include confirmation of normal newborn screening for profound T cell immunodeficiency, complete blood count with differential, quantitative serum immunoglobulins, lymphocyte subset analysis and the presence of IgG to VZV. In a child previously received VZV vaccine, the possibility of vaccine-type HZ needs to be considered. In conclusion, isolated and uncomplicated childhood HZ is unlikely to be the sole harbinger of an underlying immunodeficiency. Therefore, most children with HZ can be adequately diagnosed through medical history and readily available laboratory evaluations. The presence of concerning clinical or laboratory features, should prompt an evaluation by an experienced specialist.
Keywords: Herpes Zoster, varicella zoster virus, Pediatrics, Immunodeficencies, inborn error immunity
Received: 15 Jan 2025; Accepted: 12 Feb 2025.
Copyright: © 2025 Zhang, Kim and Grunebaum. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Eyal Grunebaum, Division of Immunology and Allergy, Hospital for Sick Children, University of Toronto, Toronto, Canada
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
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