A Rare Pediatric Case of Allopurinol-Induced Drug Reaction With Eosinophilia and Systemic Symptoms (DRESS) Successfully Treated With Intravenous Immunoglobulins.

allopurinol drug reaction drug reaction with eosinophilia and systemic symptoms immunoglobulins

Journal

The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG
ISSN: 1551-6776
Titre abrégé: J Pediatr Pharmacol Ther
Pays: United States
ID NLM: 101089851

Informations de publication

Date de publication:
Apr 2024
Historique:
received: 25 02 2022
accepted: 28 11 2022
medline: 10 4 2024
pubmed: 10 4 2024
entrez: 10 4 2024
Statut: ppublish

Résumé

Allopurinol-induced drug reaction syndrome with eosinophilia and systemic symptoms (A-DRESS) is a well-described condition in adults, whereas it is uncommon among children. We describe a case of A-DRESS in a 16-year-old male with steroid-dependent nephrotic syndrome. He presented a life-threatening clinical course with persisting fever, skin rash, eosinophilia, lymphadenopathy, distributive shock, and herpesvirus 6 detection. The withdrawal of allopurinol and a combination of intravenous immunoglobulins (IVIGs) and systemic corticosteroids led to the patient's recovery without sequelae. Drug reaction with eosinophilia and systemic symptoms (DRESS) in pediatrics is rare and can present in a severe form. Early diagnosis and timely treatment are critical for prognostic purposes. This report suggests the potentially crucial role of IVIG in the treatment of patients with A-DRESS.

Identifiants

pubmed: 38596415
doi: 10.5863/1551-6776-29.2.195
pmc: PMC11001218
doi:

Types de publication

Journal Article

Langues

eng

Pagination

195-199

Informations de copyright

Copyright. Pediatric Pharmacy Association. All rights reserved. For permissions, email: membership@pediatricpharmacy.org.

Déclaration de conflit d'intérêts

Disclosures. The authors declare no conflicts or financial interest in any product or service mentioned in the manuscript, including grants, equipment, medications, employment, gifts, and honoraria. The authors had full access to all patient information in this report and take responsibility for the integrity and accuracy of the report.

Auteurs

Gioacchino Andrea Rotulo (GA)

Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (GAR, CC, M Battaglini, M Bassi, SS), University of Genoa, Genoa, Italy.
Clinical and Research Unit of Clinical Immunology and Vaccinology (GAR), IRCCS Bambino Gesù Children Hospital, Rome, Italy.

Claudia Campanello (C)

Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (GAR, CC, M Battaglini, M Bassi, SS), University of Genoa, Genoa, Italy.

Marcella Battaglini (M)

Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (GAR, CC, M Battaglini, M Bassi, SS), University of Genoa, Genoa, Italy.

Marta Bassi (M)

Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (GAR, CC, M Battaglini, M Bassi, SS), University of Genoa, Genoa, Italy.

Carlotta Pastorino (C)

Dermatology Unit (CP), Giannina Gaslini Children's Hospital, Genoa, Italy.

Andrea Angeletti (A)

Division of Nephrology, Dialysis, and Transplantation (AA, GMG), Giannina Gaslini Children's Hospital, Genoa, Italy.

Giacomo Brisca (G)

Subintensive Care Unit (GB), IRCCS Istituto Giannina Gaslini, Genoa, Italy.

Sara Signa (S)

Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (GAR, CC, M Battaglini, M Bassi, SS), University of Genoa, Genoa, Italy.
Autoinflammatory Diseases and Immunodeficiencies Center (SS, RC), IRCCS Istituto Giannina Gaslini, Genoa, Italy.

Roberta Caorsi (R)

Autoinflammatory Diseases and Immunodeficiencies Center (SS, RC), IRCCS Istituto Giannina Gaslini, Genoa, Italy.

Gian Marco Ghiggeri (GM)

Division of Nephrology, Dialysis, and Transplantation (AA, GMG), Giannina Gaslini Children's Hospital, Genoa, Italy.

Classifications MeSH