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dc.contributorHospital General de Granollers
dc.contributor.authorRiera-Martí, Núria
dc.contributor.authorVilarrasa, E.
dc.contributor.authorLópez-Llunell, Cristina
dc.contributor.authorGamissans, Marta
dc.contributor.authorSin, M.
dc.contributor.authorRomaní, Jorge
dc.date.accessioned2024-01-30T12:22:57Z
dc.date.available2024-01-30T12:22:57Z
dc.date.issued2023-10-04
dc.identifier.citationRiera-Martí N, Vilarrasa E, López-Llunell C, Gamissans M, Sin M, Romaní J. Gluteal Hidradenitis Suppurativa: Analysis of 83 Patients. Actas Dermosifiliogr. 2023 Oct 4:S0001-7310(23)00793-7.
dc.identifier.urihttps://hdl.handle.net/11351/10937
dc.descriptionHidradenitis suppurativa; Gluteal hidradenitis; Inflammation
dc.description.abstractBackground: In 2013, Canoui-Poitrine et al. identified three hidradenitis suppurativa (HS) phenotypes by a latent class (LC) analysis, based on anatomical sites of involvement. Objective: To improve the classification of the gluteal phenotype (LC3) patients given their diverse lesion types and differences in clinical profile. Material and methods: We designed a bicentric study gathering all LC3 patients (n=83) from two hospitals. We conducted a two-step cluster analysis among them and also compared their characteristics with the rest of the HS patients (n=661). Results: Compared with global HS series, LC3 patients were more frequently non-obese men, with smoking habit, an associated arthropathy, and a more frequent history of pilonidal sinus. The analysis of LC3 patients yielded two clusters: cluster 1 (38.3%) included elderly female patients, with later diagnosis of the disease and more sinus tracts; cluster 2 (61.7%) encompassed more men with earlier disease onset and more nodules and folliculitis lesions. Limitations: The study's limitations include its retrospective nature, bicentric design, and small sample size. Conclusion: The heterogeneous clinical presentation of HS makes it essential to have a good classification of the patients. Gluteal phenotype could actually be classified into two "subphenotypes" with a different clinical profiles and management.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesActas Dermo-Sifiliográficas;
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectPell - Malalties
dc.subjectMalalties autoimmunitàries
dc.subjectPell - Inflamació
dc.subject.meshHidradenitis Suppurativa
dc.subject.meshPhenotype
dc.subject.meshAutoimmune Diseases
dc.titleGluteal Hidradenitis Suppurativa: Analysis of 83 Patients
dc.title.alternativeHidradenitis supurativa con afectación glútea: análisis de 83 pacientes
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.ad.2023.09.021
dc.subject.decshidradenitis supurada
dc.subject.decsfenotipo
dc.subject.decsenfermedades autoinmunes
dc.relation.publishversionhttps://doi.org/10.1016/j.ad.2023.09.021
dc.type.versioninfo:eu-repo/semantics/acceptedVersion
dc.audienceProfessionals
dc.contributor.authoraffiliation[Riera-Martí N, Sin M] Department of Dermatology, Hospital Universitari Parc Taulí, Sabadell, Spain. [Vilarrasa E, López-Llunell C] Department of Dermatology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain. [Gamissans M] Department of Dermatology, Hospital Universitari de Bellvitge, Hospitalet de Llobregat, Spain. [Romaní J] Department of Dermatology, Hospital General de Granollers, Granollers, Spain
dc.identifier.pmid37797882
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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