Title
Author
DOI
Article Type
Special Issue
Volume
Issue
Osseous choristoma of the tongue in a pediatric patient: a case report
1Division of Pediatric Dentistry, One Brooklyn Health Hospital, New York, NY 11212, USA
DOI: 10.22514/jocpd.2026.160 Vol.50,Issue 6,November 2026 pp.211-219
Submitted: 24 June 2026 Accepted: 25 August 2026
Published: 03 November 2026
*Corresponding Author(s): Tinnysha Chopra E-mail: tchopra@bhmcny.org
Background: Osseous choristoma is a rare benign lesion characterized by mature, histologically normal bone in an ectopic soft-tissue location. The tongue is its most common intraoral site, yet fewer than 70 cases have been reported worldwide, and pediatric cases remain especially scarce. Case: We report a case in a 15-year-old female with a firm, pedunculated posterior tongue mass first noticed by the patient at age seven and later identified incidentally during a routine primary care examination. The lesion’s long-standing clinical course, together with the histopathology findings, supports an embryological rather than a traumatic origin. The mass was successfully managed with excisional biopsy under moderate oral conscious sedation in an outpatient pediatric dental setting, avoiding the need for general anesthesia, and the diagnosis was confirmed by histopathology. At 5-month follow-up, the patient remained asymptomatic with a well-healed tongue and no evidence of recurrence, documented photographically. Conclusion: This case adds to the limited pediatric literature on lingual osseous choristoma and reviews the available evidence on preoperative imaging and prior pediatric presentations, reinforcing that this rare entity can be safely diagnosed and definitively managed within pediatric dental practice.
Osseous choristoma; Tongue lesion; Osteoma; Pedunculated mass; Surgical excision
Tinnysha Chopra, Saravanan Nambi. Osseous choristoma of the tongue in a pediatric patient: a case report. Journal of Clinical Pediatric Dentistry. 2026; 50(6): 211-219. doi: 10.22514/jocpd.2026.160
[1] Krolls SO, Jacoway JR, Alexander WN. Osseous choristomas (osteomas) of intraoral soft tissues. Oral Surgery, Oral Medicine, and Oral Pathology. 1971; 32: 588–595.
[2] Gorini E, Mullace M, Migliorini L, Mevio E. Osseous choristoma of the tongue: a review of etiopathogenesis. Case Reports in Otolaryngology. 2014; 2014: 373104.
[3] Tohill MJ, Green JG, Cohen DM. Intraoral osseous and cartilaginous choristomas: report of three cases and review of the literature. Oral Surgery, Oral Medicine, and Oral Pathology. 1987; 63: 506–510.
[4] Engel P, Cherrick HM. Extraosseous osteomas of the tongue. Journal of Oral Medicine. 1976; 31: 99–103.
[5] Supiyaphun P, Sampatanakul P, Kerekhanjanarong V, Chawakitchareon P, Sastarasadhit V. Lingual osseous choristoma: a study of eight cases and review of the literature. Ear, Nose & Throat Journal. 1998; 77: 316–325.
[6] Vered M, Lustig JP, Buchner A. Lingual osteoma: a debatable entity. Journal of Oral and Maxillofacial Surgery. 1998; 56: 9–13; discussion 14.
[7] Coté CJ, Wilson S; American Academy of Pediatrics; American Academy of Pediatric Dentistry. Guidelines for monitoring and management of pediatric patients before, during, and after sedation for diagnostic and therapeutic procedures: update 2016. Pediatrics. 2016; 138: e20161212.
[8] Andressakis DD, Pavlakis AG, Chrysomali E, Rapidis AD. Infected lingual osseous choristoma. Report of a case and review of the literature. Medicina Oral, Patología Oral y Cirugía Bucal. 2008; 13: E627–E632.
[9] Mody MD, Rocco JW, Yom SS, Haddad RI, Saba NF. Head and neck cancer. The Lancet. 2021; 398: 2289–2299.
[10] Ranganathan K, Kavitha L. Clinical aspects of oral cancer and potentially malignant disorders in South and Southeast Asia. Oral Diseases. 2025; 31: 1406–1419.
[11] Pynnonen MA, Gillespie MB, Roman B, Rosenfeld RM, Tunkel DE, Bontempo L, et al. Clinical practice guideline: evaluation of the neck mass in adults. Otolaryngology—Head and Neck Surgery. 2017; 157: S1–S30.
[12] Ramadass T, Narayanan N, Rao P, Parameswaran A. Glial heterotopia in ENT—two case reports and review of literature. Indian Journal of Otolaryngology and Head and Neck Surgery. 2011; 63: 407–410.
[13] Zhao J, Wang X, Yin F, Chu J. Early recurrent neonatal tongue glial heterotopia presenting with acute airway obstruction: the first case report. Frontiers in Pediatrics. 2026; 13: 1674740.
[14] Sun LS, Sun ZP, Ma XC, Li TJ. Glial choristoma in the oral and maxillofacial region: a clinicopathologic study of 6 cases. Archives of Pathology & Laboratory Medicine. 2008; 132: 984–988.
[15] Strome SE, McClatchey K, Kileny PR, Koopmann CF Jr. Neonatal choristoma of the tongue containing glial tissue: diagnosis and surgical considerations. International Journal of Pediatric Otorhinolaryngology. 1995; 33: 265–273.
[16] Shivamurthy A, Muniswamyreddy A, Basavaraj V. A rare case of granular cell tumour of tongue in a 13-year-old girl. Journal of Clinical & Diagnostic Research. 2024; 18: 11–13.
[17] Puricelli E, Barreiro BOB, Quevedo AS, Ponzoni D. Occurrence of dermoid cyst in the floor of the mouth: the importance of differential diagnosis in pediatric patients. Journal of Applied Oral Science. 2017; 25: 341–345.
[18] Amer SM, Ukudeyeva A, Pine HS, Campbell GA, Clement CG. Plexiform schwannoma of the tongue in a pediatric patient with neurofibromatosis type 2: a case report and review of literature. Case Reports in Pathology. 2018; 2018: 9814591.
[19] Abbasi AJ, Taheri MM, Asadi A, Bahrami R, Nikparto N. Myositis ossificans traumatica of masticatory muscles: a case report and review of the literature. Oral and Maxillofacial Surgery Cases. 2024; 10: 100361.
[20] Loyzaga JM, Fernandez Machin P, Sala J. Osteogenic sarcoma of the tongue. Case report and review of the literature. Pathology, Research and Practice. 1996; 192: 75–78; discussion 79–80.
[21] Arimoto S, Shigeoka M, Akashi M. Tongue osseous choristoma in an 11-year-old female: a case report and literature review focusing on pediatric cases. Case Reports in Dentistry. 2021; 2021: 8021362.
[22] Shareef ZJ, Shareef SJ, Kerndt CC, Aughenbaugh A, Di Ponio A. Lingual osseous choristoma: a comprehensive systematic review of lesion presentation, histology, and morphology. Spartan Medical Research Journal. 2020; 5: 17543.
[23] Turan Ş, Pınarbaşlı MÖ, Açıkalın M, Kaya E, Özüdoğru E. Lingual osseous choristoma. Turkish Archives of Otorhinolaryngology. 2016; 54: 86–88.
[24] Kim HJ, Jun SY, Lim HK. Case report: synchronous lingual osseous choristoma and suprahyoid thyroglossal duct cyst: insights into the embryological thyroglossal-hyoid axis. Frontiers in Surgery. 2026; 13: 1856644.
[25] Brennan T, Rastatter JC. Multilevel airway obstruction including rare tongue base mass presenting as severe croup in an infant. International Journal of Pediatric Otorhinolaryngology. 2013; 77: 128–129.
[26] Chai RL, Ozolek JA, Branstetter BF, Mehta DK, Simons JP. Congenital choristomas of the oral cavity in children. The Laryngoscope. 2011; 121: 2100–2106.
[27] Wei WI, Lau WF, Lam KH, Hui Y. The role of the fibreoptic bronchoscope in otorhinolaryngological practice. The Journal of Laryngology and Otology. 1987; 101: 1263–1270.
[28] Paradis TJ, Dixon J, Tieu BH. The role of bronchoscopy in the diagnosis of airway disease. Journal of Thoracic Disease. 2016; 8: 3826–3837.
[29] Yellon RF. Epiglottic and base-of-tongue prolapse in children: grading and management. The Laryngoscope. 2006; 116: 194–200.
[30] American Academy of Pediatric Dentistry. Behavior guidance for the pediatric dental patient. 2023. Available at: https://www.aapd.org/research/oral-health-policies--recommendations/behavior-guidance-for-the-pediatric-dental-patient/ (Accessed: 03 September 2026).
Top