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In this paper we report an unprecedented case of oral IgG4\u2010RD mimicking angiolymphoid hyperplasia with eosinophilia (ALHE), and another case presenting as plasma cell gingivitis. We then performed a scoping review of published cases of IgG4\u2010RD involving the oral cavity. The following data were collected for each case: age, sex, intraoral site(s) involved, clinical appearance, imaging features, serum IgG4 values, histopathology, treatment, and follow\u2010up duration. Fifty\u2010one cases of oral IgG4\u2010RD were published in literature. The hard palate and jaw bones were the two main locations reported, while the histological identification of a IgG4\/IgG plasma cells ratio\u2009\u226540% was fundamental for diagnosis. Conversely, the pathological features of storiform fibrosis and obliterative phlebitis were not common. Future reports regarding oral IgG4\u2010RD should report clear adherence to the recognized international diagnostic criteria of the disease.<\/jats:p>","DOI":"10.1002\/hed.27763","type":"journal-article","created":{"date-parts":[[2024,4,3]],"date-time":"2024-04-03T07:25:02Z","timestamp":1712129102000},"page":"1510-1525","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["The \u201cgreat imitator\u201d: <scp>IgG4<\/scp>\u2010related disease of the oral cavity. 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