Katalog Plus
Bibliothek der Frankfurt UAS
Bald neuer Katalog: sichern Sie sich schon vorab Ihre persönlichen Merklisten im Nutzerkonto: Anleitung.
Dieses Ergebnis aus Complementary Index kann Gästen nicht angezeigt werden.  Login für vollen Zugriff.

Recurrent Acute Pericarditis as the Initial Presenting Sign in an Adolescent with Primary Sjögren's Syndrome: A Case Report.

Title: Recurrent Acute Pericarditis as the Initial Presenting Sign in an Adolescent with Primary Sjögren's Syndrome: A Case Report.
Authors: Doğantan, Şeyda; Taşkın, Sema Nur; Turk, Cem Berk
Source: Innovative Journal of Pediatrics; 2026, Vol. 36 Issue 1, p1-7, 7p
Subject Terms: PERICARDITIS; AUTOIMMUNE diseases; CARDIOLOGICAL manifestations of general diseases; MYCOPHENOLIC acid; COLCHICINE; HYDROXYCHLOROQUINE; AUTOIMMUNITY
Abstract: Background: Sjögren's syndrome (SS) is a chronic autoimmune disease primarily characterized by sicca symptoms, but its presentation in children often differs significantly from that seen in adults. In pediatric cases, classic dryness is uncommon, and the diagnosis is frequently delayed due to atypical manifestations. Cardiac involvement, especially recurrent pericarditis, is sporadic in SS and has not been previously reported as the initial and sole presentation in pediatric patients. Case Presentation: We report the case of a 16-year-old male with no prior medical history who presented with recurrent pericarditis, persistent fever, and systemic symptoms. Extensive evaluation ruled out infectious, neoplastic, and autoinflammatory causes. Although the patient lacked sicca symptoms, a minor salivary gland biopsy revealed focal lymphocytic sialadenitis with a focus score of 1.76, consistent with SS. Serologic testing was notable for isolated anti-Ro52 positivity. The patient was treated with hydroxychloroquine, colchicine, and mycophenolate mofetil, achieving clinical remission during six months of follow-up. Conclusions: This case highlights an atypical presentation of pediatric SS, manifesting solely as recurrent pericarditis without glandular involvement. It underscores the need for heightened clinical suspicion and comprehensive diagnostic evaluation in children with unexplained pericarditis, as early recognition of SS is critical to initiating appropriate immunosuppressive therapy and preventing disease progression. This case underscores the importance of considering autoimmune etiologies in recurrent pericarditis and highlights the need for increased awareness regarding early recognition of primary SS in children. Future research should focus on better defining pediatric manifestations and improving long-term follow-up strategies. [ABSTRACT FROM AUTHOR]
: Copyright of Innovative Journal of Pediatrics is the property of Brieflands and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Complementary Index