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REVIEW

Oral glomus tumor: A systematic review highlighting clinical and histopathological characteristics of a time-reclassified entity

Eliano Cascardi1 Fabio Maglitto2 Mario Della Mura1 Gerardo Cazzato1 Stefan Cocis2 Angelo Michele Inchingolo3 Francesca Calò3 Sharon Di Serio3 Antonio Musciacchio3 Francesco Inchingolo3* Chiara Copelli2 Andrea Palermo4 Alessio Danilo Inchingolo3 Gianna Dipalma3
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1 Pathology section of Department of Precision and Regenerative Medicine and Ionian Area (DiMePre-J), Faculty of Medicine, University of Bari “Aldo Moro”, Bari, Apulia, Italy
2 Maxillo-Facial Surgery Unit, Interdisciplinary Department of Medicine, Faculty of Medicine, Aldo Moro University of Bari, Bari, Apulia, Italy
3 Department of Medicine, Faculty of Medicine, University of Bari “Aldo Moro”, Bari, Apulia, Italy
4 Department of Experimental Medicine, Faculty of Medicine, University of Salento, Lecce, Apulia, Italy
Received: 3 February 2026 | Revised: 10 March 2026 | Accepted: 30 April 2026 | Published online: 20 July 2026
© 2026 by the Author(s). This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution -Noncommercial 4.0 International License (CC-by the license) ( https://creativecommons.org/licenses/by-nc/4.0/ )
Abstract

Oral glomus tumors are exceptionally rare perivascular neoplasms that are frequently misdiagnosed due to their nonspecific clinical presentation. Their rarity has historically resulted in inconsistent terminology and a limited understanding of their biological behavior. This systematic review was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses 2020 guidelines and registered in the International Prospective Register of Systematic Reviews (ID 1175198). A comprehensive literature search of PubMed, Scopus, and Web of Science (1954–2024) was performed to identify English-language case reports and case series describing histologically confirmed oral glomus tumors. Extracted data included demographics, tumor location and size, histopathological features, treatment modalities, recurrence, and follow-up. A total of 740 records were identified, of which 31 studies met the inclusion criteria, yielding 34 confirmed cases of oral glomus tumor. Patients ranged from 8 to 85 years, with a slight male predominance. The most frequently affected site was the lip, followed by the tongue, palatal mucosa, and other intraoral soft tissues. Tumor size varied from 0.3 to 4.5 cm. Classic glomus tumor was the most common subtype, with occasional reports of glomangiomyoma and one case of glomangiosarcoma. Surgical excision was curative in most patients. Recurrence occurred in a minority of cases, but metastasis was not reported in the only case of glomangiosarcoma. Oral glomus tumors are predominantly benign, well-circumscribed lesions with excellent prognosis following complete surgical excision. Accurate diagnosis relies on thorough histopathological and immunohistochemical evaluation, given the potential overlap with other mesenchymal tumors. This review provides the most updated synthesis of clinical, pathological, and outcome features of oral glomus tumors.

Keywords
Oral glomus tumor
Glomuvenous malformation
Glomangiomyoma
Malignant glomus tumor
Oral cavity
Oral mesenchymal tumor
Funding
None.
Conflict of interest
The authors declare no conflict of interest.
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