{"title":"Síndromes autoinflamatorios en edad adulta: reporte de 8 casos","authors":"Nuria Garvín Grande , Paloma Turiel Hernández , Manuel Beladiez Giner , Giancarlo Ernesto Candela Ganoza , Nicolás Silvestre Torner , Paz Collado Ramos","doi":"10.1016/j.reuma.2026.502126","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Retrospective study documenting the clinical features, demographic and analytical parameters and therapeutic management in a cohort of adult patients with AIS.</div></div><div><h3>Clinical description</h3><div>Eight patients (50% male) were included, the majority of whom were Caucasian. The most frequent AIS was AOSD (37.5%). The mean age at symptom onset was 40<!--> <!-->±<!--> <!-->23.1 years. The mean diagnostic delay was 5.7<!--> <!-->±<!--> <!-->5 years. Fever, skin rash and myalgias were the most prevalent symptoms. The mean CRP value was 187.1<!--> <!-->±<!--> <!-->110<!--> <!-->mg/L and ESR rate of 95.2<!--> <!-->±<!--> <!-->38<!--> <!-->mm/h. 100% were treated with systemic corticosteroids, 50% with int i-IL-1. Three patients required a switch from anakinra to canakinumab due to intolerance or lack of efficacy.</div></div><div><h3>Conclusions</h3><div>Given its increasing prevalence, this study emphasizes the importance of not underestimating the existence of AIS in adults, regardless of the level of health care. Early diagnosis and treatment with i-IL-1 are essential to control disease activity and prevent serious complications.</div></div>","PeriodicalId":47115,"journal":{"name":"Reumatologia Clinica","volume":"22 4","pages":"Article 502126"},"PeriodicalIF":1.3000,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reumatologia Clinica","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1699258X26000513","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/3/19 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction
Retrospective study documenting the clinical features, demographic and analytical parameters and therapeutic management in a cohort of adult patients with AIS.
Clinical description
Eight patients (50% male) were included, the majority of whom were Caucasian. The most frequent AIS was AOSD (37.5%). The mean age at symptom onset was 40 ± 23.1 years. The mean diagnostic delay was 5.7 ± 5 years. Fever, skin rash and myalgias were the most prevalent symptoms. The mean CRP value was 187.1 ± 110 mg/L and ESR rate of 95.2 ± 38 mm/h. 100% were treated with systemic corticosteroids, 50% with int i-IL-1. Three patients required a switch from anakinra to canakinumab due to intolerance or lack of efficacy.
Conclusions
Given its increasing prevalence, this study emphasizes the importance of not underestimating the existence of AIS in adults, regardless of the level of health care. Early diagnosis and treatment with i-IL-1 are essential to control disease activity and prevent serious complications.
期刊介绍:
Una gran revista para cubrir eficazmente las necesidades de conocimientos en una patología de etiología, expresividad clínica y tratamiento tan amplios. Además es La Publicación Oficial de la Sociedad Española de Reumatología y del Colegio Mexicano de Reumatología y está incluida en los más prestigiosos índices de referencia en medicina.