Treatments of tenosynovial giant cell tumours of the temperomandibular joint: a report of three cases and a review of literature
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Publication year
2018Source
International Journal of Oral and Maxillofacial Surgery, 47, 10, (2018), pp. 1288-1294ISSN
Publication type
Article / Letter to editor
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Organization
Orthopaedics
Oral and Maxillofacial Surgery
Neurosurgery
Pathology
Journal title
International Journal of Oral and Maxillofacial Surgery
Volume
vol. 47
Issue
iss. 10
Page start
p. 1288
Page end
p. 1294
Subject
Radboudumc 0: Other Research RIHS: Radboud Institute for Health Sciences; Radboudumc 10: Reconstructive and regenerative medicine RIHS: Radboud Institute for Health Sciences; Radboudumc 9: Rare cancers RIHS: Radboud Institute for Health Sciences; Radboudumc 9: Rare cancers RIMLS: Radboud Institute for Molecular Life Sciences; Neurosurgery - Radboud University Medical Center; Oral and Maxillofacial Surgery - Radboud University Medical Center; Orthopaedics - Radboud University Medical Center; Pathology - Radboud University Medical CenterAbstract
Tenosynovial giant cell tumours (TGCTs) are benign lesions affecting synovial joints. The classified subtypes are localized and diffuse. They seldom occur in the temporomandibular joint (TMJ). The aim of this study is to report on three new cases and to review the literature. One patient had surgical debulking with adjuvant external beam radiation therapy (EBRT). After 1year of follow-up, no evidence of disease was presented. The second patient was misdiagnosed and treated with denosumab. Debulking with adjuvant EBRT followed. Ten months postoperatively, no disease progression was seen. The third patient received systemic nilotinib and remained stable for over 5years. The literature review included 106 cases of which 95 had diffuse subtype. Most patients, had surgical excision. Thirteen (14%) patients received adjuvant EBRT. Eleven (14%) recurrences were identified. After 1-, 5- and 10 years of follow-up, an overall progression-free survival (PFS) of 99% (95% confidence interval (CI) 0.96-1), 80% (95% CI 0.68-0.94), 67% (95% CI 0.51-0.90) was calculated, respectively. Treatments for diffuse-TGCT-TMJ should be individualized depending on age, severity of symptoms, extent of disease and progression, expected mutilation of surgical interference, and current systemic treatment options. In stable disease a 'wait and see' policy, is a viable option. Additional treatments should be reserved for symptomatic, irresectable tumours or residual disease after surgical treatment with persistent complaints.
This item appears in the following Collection(s)
- Academic publications [246216]
- Electronic publications [133864]
- Faculty of Medical Sciences [93266]
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