Wells syndrome and acquired cutis laxa: An atypical association.
The Journal of dermatology(2023)
摘要
The Journal of DermatologyEarly View LETTER TO THE EDITOR Wells syndrome and acquired cutis laxa: An atypical association Margot Bouquerel, Corresponding Author Margot Bouquerel [email protected] orcid.org/0000-0002-3159-4935 Service de Dermatologie, CHU de Bordeaux, Bordeaux, France Correspondence Margot Bouquerel, 44 avenue Vergniaud, 94100 Saint-Maur-des-Fosses, France. Email: [email protected]Search for more papers by this authorLaure Dequidt, Laure Dequidt Service de Dermatologie, CHU de Bordeaux, Bordeaux, FranceSearch for more papers by this authorMarie-Laure Jullie, Marie-Laure Jullie Service de Pathologie, Hôpital Haut Lévêque, CHU de Bordeaux, Bordeaux, FranceSearch for more papers by this authorFanny Beltzung, Fanny Beltzung Service de Pathologie, Hôpital Haut Lévêque, CHU de Bordeaux, Bordeaux, FranceSearch for more papers by this authorJean-Baptiste Gibier, Jean-Baptiste Gibier Institut de Pathologie, Centre de Biologie Pathologie, CHU de Lille, Lille, FranceSearch for more papers by this authorGuillaume Lefevre, Guillaume Lefevre Centre de référence des syndromes hyperéosinophiliques, Service de Médecine interne et Immunologie Clinique, U1286 INSERM INFINITE Institute for Translationnel Research in Inflammation, Lille, FranceSearch for more papers by this authorFrederic Dezoteux, Frederic Dezoteux Service de Dermatologie, CHU de Lille, U1286 INSERM INFINITE Institute for Translationnel Research in Inflammation, Lille, FranceSearch for more papers by this authorFanny Morice-Picard, Fanny Morice-Picard Service de Dermatologie, CHU de Bordeaux, Bordeaux, France Service de Dermatologie, Centre de référence des maladies rares de la peau, CHU de Bordeaux, Bordeaux, FranceSearch for more papers by this authorAurelien Trimouille, Aurelien Trimouille Service de Dermatologie, Centre de référence des maladies rares de la peau, CHU de Bordeaux, Bordeaux, France Service de Pathologie Hôpital Pellegrin, CHU de Bordeaux, Bordeaux, FranceSearch for more papers by this authorMarie-Sylvie Doutre, Marie-Sylvie Doutre Service de Dermatologie, CHU de Bordeaux, Bordeaux, FranceSearch for more papers by this author Margot Bouquerel, Corresponding Author Margot Bouquerel [email protected] orcid.org/0000-0002-3159-4935 Service de Dermatologie, CHU de Bordeaux, Bordeaux, France Correspondence Margot Bouquerel, 44 avenue Vergniaud, 94100 Saint-Maur-des-Fosses, France. Email: [email protected]Search for more papers by this authorLaure Dequidt, Laure Dequidt Service de Dermatologie, CHU de Bordeaux, Bordeaux, FranceSearch for more papers by this authorMarie-Laure Jullie, Marie-Laure Jullie Service de Pathologie, Hôpital Haut Lévêque, CHU de Bordeaux, Bordeaux, FranceSearch for more papers by this authorFanny Beltzung, Fanny Beltzung Service de Pathologie, Hôpital Haut Lévêque, CHU de Bordeaux, Bordeaux, FranceSearch for more papers by this authorJean-Baptiste Gibier, Jean-Baptiste Gibier Institut de Pathologie, Centre de Biologie Pathologie, CHU de Lille, Lille, FranceSearch for more papers by this authorGuillaume Lefevre, Guillaume Lefevre Centre de référence des syndromes hyperéosinophiliques, Service de Médecine interne et Immunologie Clinique, U1286 INSERM INFINITE Institute for Translationnel Research in Inflammation, Lille, FranceSearch for more papers by this authorFrederic Dezoteux, Frederic Dezoteux Service de Dermatologie, CHU de Lille, U1286 INSERM INFINITE Institute for Translationnel Research in Inflammation, Lille, FranceSearch for more papers by this authorFanny Morice-Picard, Fanny Morice-Picard Service de Dermatologie, CHU de Bordeaux, Bordeaux, France Service de Dermatologie, Centre de référence des maladies rares de la peau, CHU de Bordeaux, Bordeaux, FranceSearch for more papers by this authorAurelien Trimouille, Aurelien Trimouille Service de Dermatologie, Centre de référence des maladies rares de la peau, CHU de Bordeaux, Bordeaux, France Service de Pathologie Hôpital Pellegrin, CHU de Bordeaux, Bordeaux, FranceSearch for more papers by this authorMarie-Sylvie Doutre, Marie-Sylvie Doutre Service de Dermatologie, CHU de Bordeaux, Bordeaux, FranceSearch for more papers by this author First published: 12 July 2023 https://doi.org/10.1111/1346-8138.16897Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES 1Peckruhn M, Elsner P, Tittelbach J. Eosinophilic dermatoses. J Dtsch Dermatol Ges. 2019; 17: 1039–1051. 2Räßler F, Lukács J, Elsner P. Treatment of eosinophilic cellulitis (Wells syndrome) – a systematic review. J Eur Acad Dermatol Venereol. 2016; 30: 1465–1479. 3Lebwohl MG, Schwartz E, Jacobs L, Lebwohl M, Sakai L, Fleischmajer R. Abnormalities of fibrillin in acquired cutis laxa. J Am Acad Dermatol. 1994; 30: 950–954. 4Fauconneau A, Sokolowski N, Camus M, Darrigade AS, Guillet S, Jullie ML, et al. Acquired cutis laxa associated with neutrophilic urticarial dermatosis. Int J Dermatol. 2021; 60: 771–772. 5Hu Q, Reymond J-L, Pinel N, Zabot M-T, Urban Z. Inflammatory destruction of elastic fibers in acquired cutis laxa is associated with missense alleles in the elastin and fibulin-5 genes. J Invest Dermatol. 2006; 126: 283–290. 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cutis laxa,syndrome,wells
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