Paediatrics & child health · 2026
Juvenile recurrent parotitis: a paediatric rheumatology perspective.
СтатьяНазвание и аннотация: Перевод в очереди
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Öztürk Didem, Çelikel Elif, Tekin Zahide Ekici, Karagöl Cüneyt, Ertem Şeyma, Polat Merve Cansu, Özçelik Emine, Ekici Mehveş Işıklar, Es Yasemin Uğur, Yoğun Sultan Nilay, Erdem Torun Şeyma, Özkaya Parlakay Aslınur, Keçeli Avni Merter, Acar Banu
Аннотация
OBJECTIVE: The purpose of this study was to evaluate the demographic characteristics, clinical and laboratory findings, imaging methods and treatment of juvenile recurrent parotitis (JRP) patients.
METHOD: This observational medical record study was conducted in patients, aged 1 to18 years, were diagnosed with JRP.
RESULTS: Of the 46 patients with JRP included, 27 (58.7%) were male. The median age at onset was 4 years, and the median age at diagnosis was 6.5 years. Thirty-seven (80.4%) of JRP patients were idiopathic. The underlying causes were as follow: inborn errors of immunity (n = 3, 6.5%), rheumatologic (n = 2, 4.3%), infectious diseases (n = 2, 4.3%), congenital anomaly (n = 431, 2.2%), and one patient (2.2%) had both rheumatologic disease and inborn errors of immunity. Two patients (4.3%) were diagnosed with Sjögren syndrome, and one patient (2.2%) was diagnosed with IgG4-related disease.
CONCLUSION: Although most JRP is idiopathic, some patients may have infectious, structural, immunologic or autoimmune abnormalities.
METHOD: This observational medical record study was conducted in patients, aged 1 to18 years, were diagnosed with JRP.
RESULTS: Of the 46 patients with JRP included, 27 (58.7%) were male. The median age at onset was 4 years, and the median age at diagnosis was 6.5 years. Thirty-seven (80.4%) of JRP patients were idiopathic. The underlying causes were as follow: inborn errors of immunity (n = 3, 6.5%), rheumatologic (n = 2, 4.3%), infectious diseases (n = 2, 4.3%), congenital anomaly (n = 431, 2.2%), and one patient (2.2%) had both rheumatologic disease and inborn errors of immunity. Two patients (4.3%) were diagnosed with Sjögren syndrome, and one patient (2.2%) was diagnosed with IgG4-related disease.
CONCLUSION: Although most JRP is idiopathic, some patients may have infectious, structural, immunologic or autoimmune abnormalities.