A case of childhood Sjögren’s syndrome diagnosed due to bilateral plunging ranula

نویسندگان

چکیده

We report a case of childhood Sjögren’s syndrome (CSS) in 13-year-old girl, diagnosed due to bilateral plunging ranula. (SS) is an autoimmune disease which various autoantibodies appear, mainly sialadenitis and dacryoadenitis. Plunging ranula salivary gland often encountered daily clinical work. It considered be one the symptoms SS, but this not widely known. MRI scans showed fluid retention bottom mouth on both sides, suggesting Laboratory examination positivity for anti-Ro/SS-A antibody, anti-La/SS-B immunoglobulin G (IgG), rheumatoid factor (RF) antinuclear indicating CSS. Fenestration lip biopsy were performed, histopathological minor revealed chronic inflammation; hence, diagnosis CSS was made. Examination rheumatology department no extraglandular symptoms, treatment policy conduct follow up. A favorable outcome achieved, with evidence recurrence two years postoperatively.

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ژورنال

عنوان ژورنال: Japanese Journal of Oral and Maxillofacial Surgery

سال: 2023

ISSN: ['0021-5163', '2186-1579']

DOI: https://doi.org/10.5794/jjoms.69.281