Tamponnade révélant une maladie de Still de l'adulte : à propos de deux observations

Ghorbel, I. Ben; Lamloum, M.; Miled, M.; Aoun, Naji; Houman, M.H.; Pouchot, J.

doi:10.1016/j.revmed.2006.03.027

Cited by 10 publications

(2 citation statements)

References 13 publications

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“…In AOSD, pericarditis is also known as one of the most frequent systemic manifestations,12 17–19 tamponade being potentially life-threatening,17 but only 14 cases of myocardial involvement are well documented in the literature in current languages (table 1); three other case reports have been published 20–22…”

Section: Discussionmentioning

confidence: 99%

Adult-onset Still's disease revealed by perimyocarditis and a concomitant reactivation of an EBV infection

et al. 2012

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SummaryWe describe a 17-year-old patient presenting perimyocarditis as the initial manifestation of the adult-onset Still's disease. Corticotherapy was rapidly successful but induced major acute hepatitis in relation with Epstein-Barr virus reactivation. After 1 year, even if the global outcome is favourable, a slightly lowered ejection fraction still persists. Former case reports and differential diagnosis with reactive haemophagocytic syndrome would be discussed. BACKGROUND

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Section: Discussionmentioning

confidence: 99%

Adult-onset Still's disease revealed by perimyocarditis and a concomitant reactivation of an EBV infection

et al. 2012

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“…Cardiac involvement, predominantly pericarditis, is estimated to occur clinically in 10% of cases, and echocardiographic signs are observed in more than 30% of the cases (36, 37). Pericardial tamponade is uncommon, especially after therapy has been undertaken (38). Children and adolescents suffering from other forms of JIA might have asymptomatic pericardial effusion or a typically mild and benign pericarditis in up to 30 and 10% of cases, respectively (39).…”

Section: Etiology Epidemiology and Diagnosismentioning

confidence: 99%

Recurrent Pericarditis in Children and Adolescents

et al. 2019

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Recurrent pericarditis (RP) is a clinical syndrome characterized by recurrent attacks of acute pericardial inflammation. Prognosis quoad vitam is good, although morbidity might be significant, especially in children and adolescents. Multiple potential etiologies result in RP, in the vast majority of cases through autoimmune or autoinflammatory mechanisms. Idiopathic RP is one of the most frequent diagnoses, that requires the exclusion of all known etiologies. Therapeutic advances in the last decade have been significant with the recognition of the effectiveness of anti IL1 therapy, but a correct diagnostic and therapeutic algorithm is of key importance. Unfortunately, most of evidence comes from studies in adult patients. Here we review the etiopathogenesis, diagnosis and management of RP in pediatric patients.

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