Clinical, Laboratory, and Interferon-Alpha Response Characteristics of Patients With Chilblain-like Lesions During the COVID-19 Pandemic.


Journal

JAMA dermatology
ISSN: 2168-6084
Titre abrégé: JAMA Dermatol
Pays: United States
ID NLM: 101589530

Informations de publication

Date de publication:
01 02 2021
Historique:
pubmed: 26 11 2020
medline: 12 3 2021
entrez: 25 11 2020
Statut: ppublish

Résumé

Chilblain-like lesions have been reported during the coronavirus 2019 (COVID-19) pandemic. The pathophysiology of such manifestations remains largely unknown. To perform a systematic clinical, histologic, and biologic assessment in a cohort of patients with chilblain-like lesions occurring during the COVID-19 pandemic. In this prospective case series carried out with a COVID-19 multidisciplinary consultation group at the University Hospital of Nice, France, 40 consecutive patients presenting with chilblain-like lesions were included. Patients underwent a thorough general and dermatologic examination, including skin biopsies, vascular investigations, biologic analyses, interferon-alpha (IFN-α) stimulation and detection, and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) polymerase chain reaction (PCR) and serologic analysis. Overall, 40 consecutive patients with chilblain-like lesions were included. Most patients were young, with a median (range) age of 22 (12-67) years; 19 were male and 21 were female. The clinical presentation was highly reproducible with chilblain-like lesions mostly on the toes. Bullous and necrotic evolution was observed in 11 patients. Acrocyanosis or cold toes were reported in 19 (47.5%) cases. Criteria compatible with COVID-19 cases were noted in 11 (27.5%) within 6 weeks prior to the eruption. The real-time PCR (rt-PCR) testing results were negative in all cases. Overall, SARS-CoV-2 serology results were positive in 12 patients (30%). D-dimer concentration levels were elevated in 24 (60.0%) cases. Cryoglobulinemia and parvovirus B19 serologic results were negative for all tested patients. The major histologic findings were features of lymphocytic inflammation and vascular damage with thickening of venule walls and pericyte hyperplasia. A significant increase of IFN-α production after in vitro stimulation was observed in the chilblain population compared with patients with mild-severe acute COVID-19. Taken together, our results suggest that chilblain-like lesions observed during the COVID-19 pandemic represent manifestations of a viral-induced type I interferonopathy. ClinicalTrials.gov Identifier: NCT04344119.

Identifiants

pubmed: 33237291
pii: 2773121
doi: 10.1001/jamadermatol.2020.4324
pmc: PMC7689569
doi:

Substances chimiques

Interferon-alpha 0

Banques de données

ClinicalTrials.gov
['NCT04344119']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

202-206

Auteurs

Thomas Hubiche (T)

Department of Dermatology, Université Côte d'Azur, CHU Nice, Nice, France.

Nathalie Cardot-Leccia (N)

Department of Pathology, Université Côte d'Azur, CHU Nice, Nice, France.

Florence Le Duff (F)

Department of Dermatology, Université Côte d'Azur, CHU Nice, Nice, France.

Barbara Seitz-Polski (B)

Department of Immunology, Université Côte d'Azur, UPR 01, UR2CA, CHU Nice, Nice, France.

Pascal Giordana (P)

Department of Vascular Medicine, Université Côte d'Azur, CHU Nice, Nice, France.

Christine Chiaverini (C)

Department of Dermatology, Université Côte d'Azur, CHU Nice, Nice, France.

Valérie Giordanengo (V)

Department of Virology, Université Côte d'Azur, CHU Nice, Nice, France.
Université Côte d'Azur, INSERM, U1065, C3M, Nice, France.

Géraldine Gonfrier (G)

Department of Virology, Université Côte d'Azur, CHU Nice, Nice, France.

Vincent Raimondi (V)

Cerballiance Côte d'Azur, Cagnes-sur-Mer, France.

Olivier Bausset (O)

Cerballiance Côte d'Azur, Cagnes-sur-Mer, France.

Zoubir Adjtoutah (Z)

Cerballiance Côte d'Azur, Cagnes-sur-Mer, France.

Margaux Garnier (M)

Department of Dermatology, Université Côte d'Azur, CHU Nice, Nice, France.

Fanny Burel-Vandenbos (F)

Department of Pathology, Université Côte d'Azur, CHU Nice, Nice, France.

Bérengère Dadone-Montaudié (B)

Department of Pathology, Université Côte d'Azur, CHU Nice, Nice, France.
Laboratory of Solid Tumors Genetics, Université Côte d'Azur, CHU Nice, Nice, France.
Institute for Research on Cancer and Aging of Nice (IRCAN), Université Côte d'Azur, CNRS UMR 7284/INSERM U1081, Nice, France.

Véréna Fassbender (V)

Department of Vascular Medicine, Université Côte d'Azur, CHU Nice, Nice, France.

Aurélia Palladini (A)

Department of Dermatology, Université Côte d'Azur, CHU Nice, Nice, France.

Johan Courjon (J)

Department of Infectiology, Université Côte d'Azur, CHU Nice, Nice, France.

Véronique Mondain (V)

Department of Infectiology, Université Côte d'Azur, CHU Nice, Nice, France.

Julie Contenti (J)

Emergency Department, Université Côte d'Azur, CHU Nice, Nice, France.

Jean Dellamonica (J)

Medical Intensive Care Unit, Université Côte d'Azur, UPR 01, UR2CA, CHU Nice, Nice, France.

Georges Leftheriotis (G)

Department of Vascular Medicine, Université Côte d'Azur, CHU Nice, Nice, France.

Thierry Passeron (T)

Department of Dermatology, Université Côte d'Azur, CHU Nice, Nice, France.
Université Côte d'Azur, INSERM, U1065, C3M, Nice, France.

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