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Severe Facial Herpes Vegetans and Viremia in NFKB2-Deficient Common Variable Immunodeficiency.
Parsons, Karyn; Cipriano, Sarah D; Rosen, Lindsey B; Browne, Sarah K; Walter, Jolan E; Stone, Bryan L; Keeshin, Susana; Chen, Karin.
Afiliación
  • Parsons K; Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT, United States.
  • Cipriano SD; Department of Dermatology, University of Utah School of Medicine, Salt Lake City, UT, United States.
  • Rosen LB; Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.
  • Browne SK; Center for Biologics Evaluation and Research, Food and Drug Administration, Silver Spring, MD, United States.
  • Walter JE; Division of Allergy and Immunology, Department of Pediatrics, Johns Hopkins All Children's Hospital, St. Petersburg, FL, United States.
  • Stone BL; Division of Allergy and Immunology, Department of Pediatrics, Morsani College of Medicine, University of South Florida, Tampa, FL, United States.
  • Keeshin S; Division of Allergy and Immunology, Department of Pediatrics, Massachusetts General Hospital for Children, Boston, MA, United States.
  • Chen K; Division of Pediatric Inpatient Medicine, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT, United States.
Front Pediatr ; 7: 61, 2019.
Article en En | MEDLINE | ID: mdl-30941333
ABSTRACT
With the accessibility of next-generation sequencing modalities, an increasing number of primary immunodeficiency disorders (PIDDs) such as common variable immunodeficiency (CVID) have gained improved understanding of molecular pathogenesis and disease phenotype with the identification of a genetic etiology. We report a patient with early-onset CVID due to an autosomal dominant loss-of-function mutation in NFKB2 who developed a severe herpes vegetans cutaneous infection as well as concurrent herpes simplex virus viremia. The case highlights features of CVID, unique aspects of NF-κB2 deficiency including susceptibility to herpesvirus infections, the detection of neutralizing anticytokine antibodies, and the complexity of medical management of patients with a PIDD that can be aided by a known genetic diagnosis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Pediatr Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Pediatr Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos
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