Hyper-IgE syndrome in an 11 year old female presenting with acneiform rash.


Journal

Skin health and disease
ISSN: 2690-442X
Titre abrégé: Skin Health Dis
Pays: England
ID NLM: 9918227353706676

Informations de publication

Date de publication:
Feb 2024
Historique:
received: 06 07 2023
revised: 09 08 2023
accepted: 15 09 2023
medline: 5 2 2024
pubmed: 5 2 2024
entrez: 5 2 2024
Statut: epublish

Résumé

Hyper-IgE (HIES) is a rare, primary immunodeficiency characterised by eczema, recurrent staphylococcal infections, pneumonia, increased serum IgE and eosinophilia. We present the case of an 11-year-old girl presenting to dermatology with an acneiform facial rash and associated bacterial lymphadenitis. History was significant for otitis media, primary tooth retention, low impact wrist fracture, infantile acne and an absence of eczema or pneumonia. Investigations demonstrated mildly elevated IgE, normal eosinophils but positivity for a STAT3 gene mutation-thus representing a case of HIES presenting as an acneiform facial rash with absence of other primary immunological features.

Identifiants

pubmed: 38312258
doi: 10.1002/ski2.297
pii: SKI2297
pmc: PMC10831543
doi:

Types de publication

Case Reports

Langues

eng

Pagination

e297

Informations de copyright

© 2023 The Authors. Skin Health and Disease published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists.

Déclaration de conflit d'intérêts

None to declare.

Auteurs

Berbie Byrne (B)

Department of Dermatology University Hospital Galway Galway Ireland.

Tom Hefferon (T)

Department of Dermatology University Hospital Galway Galway Ireland.

Rob Harrington (R)

Department of Dermatology University Hospital Galway Galway Ireland.

Marion Leahy (M)

Department of Dermatology University Hospital Galway Galway Ireland.

Annette Murphy (A)

Department of Dermatology University Hospital Galway Galway Ireland.

Classifications MeSH