Accurate diagnosis of acute hemorrhagic edema of infancy: a French multicenter observational study.

Acute hemorrhagic edema of infancy Finkelstein-Seidlmayer vasculitis Leukocytoclastic vasculitis Observational study Pediatric dermatology Purpura

Journal

European journal of pediatrics
ISSN: 1432-1076
Titre abrégé: Eur J Pediatr
Pays: Germany
ID NLM: 7603873

Informations de publication

Date de publication:
Sep 2023
Historique:
received: 29 03 2023
accepted: 04 07 2023
revised: 29 06 2023
pubmed: 11 7 2023
medline: 11 7 2023
entrez: 11 7 2023
Statut: ppublish

Résumé

The purpose of the study is to highlight clinical signs that are either suggestive of or against the diagnosis of AHEI to improve diagnosis and management. The medical records of children under 3 years old diagnosed with AHEI were retrospectively reviewed. Clinical data and photographs were reviewed by three independent experts, and the cases were classified as probable, doubtful, or unclear AHEI. Of the 69 cases of children diagnosed with AHEI included in 22 centers, 40 were classified as probable, 22 as doubtful, and 7 as unclear. The median age of patients with probable AHEI was 11 months [IQR 9-15], and they were in overall good condition (n = 33/40, 82.5%). The morphology of the purpura was targetoid in 75% of cases (n = 30/40) and ecchymotic in 70% of cases (n = 28/40) and affected mostly the legs (n = 39/40, 97%), the arms (n = 34/40, 85%), and the face (n = 33/40, 82.5%). Edema was observed in 95% of cases and affected mostly the hands (n = 36/38, 95%) and feet (n = 28/38, 74%). Pruritus was absent in all patients with probable AHEI and described for 6/21 with doubtful AHEI (29%). AHEI was the original diagnosis in only 24 patients (n = 24/40, 60%). The major differential diagnoses were purpura fulminans and urticaria multiforme.  Conclusion: AHEI, which the diagnosis is made on clinical findings, is often misdiagnosed. Purpuric lesions localized on the face/ears, arms/forearms, and thighs/legs with edema of the hands without pruritus in a young child with a good overall condition are highly suggestive of AHEI. What is Known: •Acute hemorrhagic edema of infancy (AHEI) is a cutaneous leukocytoclastic vasculitis affecting children under 3 years old. •Appropriate diagnosis is important to distinguish this benign disease from more serious diseases to avoid investigations and treatments, iatrogenic harm and unnecessary follow-up. What is New: •AHEI is an uncommon disorder often misdiagnosed by pediatricians and dermatologists. •Purpuric lesions localized on the face/ears, arms/forearms, and thighs/legs with edema of the hands without pruritus in an infant with a good overall condition are highly suggestive of AHEI.

Identifiants

pubmed: 37432503
doi: 10.1007/s00431-023-05098-7
pii: 10.1007/s00431-023-05098-7
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4133-4141

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Sophie Leducq (S)

Department of Dermatology and Reference Center for Rare Diseases and Vascular Malformations (MAGEC), Unit of Pediatric Dermatology, CHRU Tours, Tours, France. sophie.leducq@univ-tours.fr.
Universities of Tours and Nantes, INSERM 1246-SPHERE, , Tours, France. sophie.leducq@univ-tours.fr.

Annabel Maruani (A)

Department of Dermatology and Reference Center for Rare Diseases and Vascular Malformations (MAGEC), Unit of Pediatric Dermatology, CHRU Tours, Tours, France.
Universities of Tours and Nantes, INSERM 1246-SPHERE, , Tours, France.

Christine Bodemer (C)

Department of Dermatology and Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), APHP, Paris University, Necker-Enfants Malades Hospital, Paris Centre University, Imagine Institute, Paris, France.

Sandra Biscardi (S)

Department of Pediatrics, CHI Créteil, Créteil, France.

Olivia Boccara (O)

Department of Dermatology and Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), APHP, Paris University, Necker-Enfants Malades Hospital, Paris Centre University, Imagine Institute, Paris, France.

Marie-France Chinazzo (MF)

Department of Pediatrics, CHRU Tours, Tours, France.

Emmanuel Mahé (E)

Department of Dermatology, Hôpital Victor Dupouy, Argenteuil, France.

Patrice Plantin (P)

Department of Dermatology, Quimper, Quimper, CH, France.

Sylvie Fraitag (S)

Pathology Department, Necker-Enfants Malades Hospital, APHP, Paris, France.

Juliette Mazereeuw-Hautier (J)

Department of Dermatology, CHU Toulouse, Toulouse, France.

Christine Chiaverini (C)

Department of Dermatology, University Hospital of Nice, Nice, France.

Irene Lemelle (I)

Paediatric Onco-Haematology, Brabois Hospital, University Hospital of Nancy, Vandoeuvre-Lès-Nancy, France.

Didier Bessis (D)

Department of Dermatology, University Hospital of Montpellier, Montpellier, France.

Emmanuelle Bourrat (E)

Department of General Pediatrics, Robert Debré University Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.

Stéphanie Mallet (S)

Department of Dermatology, Hôpital Timone, Aix-Marseille Université, Marseille, France.

Bertille Bonniaud (B)

Department of Dermatology and Genetics of Developmental Anomalies, UMR Inserm 1231, François-Mitterrand University Hospital, 14 Rue Paul Gaffarel, BP 77908, 21079, Dijon, France.

Martine Grall-Lerosey (M)

Department of Pediatrics, CHU Rouen, Rouen, France.

Ludovic Martin (L)

Department of Dermatology, CHU Angers, Angers, France.

Franck Boralevi (F)

Pediatric Dermatology Unit, Hôpital Pellegrin-Enfants, CHU de Bordeaux, France.

Maryam Piram (M)

Department of Pediatrics, CHU Sainte Justine Research Centre, Sainte Justine University Hospital, University of Montreal, Montreal, QC, Canada.

Classifications MeSH