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ArticleOral and maxillofacial surgery2025

Temporomandibular joint ankylosis following bimaxillary surgery in a patient with neurofibromatosis type 1: a case report.

Alexandra Delay, Andrea Varazzani, Cyril Bouland, Louis Brochet, Pierre Bouletreau, Anne-Sabine Cousin

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Article in Oral and maxillofacial surgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Alexandra DelayDepartment of oral and maxillo-facial surgery, University Hospital Lyon Sud, Lyon, France. delaya20@gmail.com.ORCID http://orcid.org/0000-0002-4831-440X
Andrea VarazzaniDepartment of oral and maxillo-facial surgery, University Hospital Lyon Sud, Lyon, France.
Cyril BoulandDepartment of oral and maxillo-facial surgery, University Hospital Lyon Sud, Lyon, France.
Louis BrochetDepartment of oral and maxillo-facial surgery, University Hospital Lyon Sud, Lyon, France.
Pierre BouletreauDepartment of oral and maxillo-facial surgery, University Hospital Lyon Sud, Lyon, France.
Anne-Sabine CousinDepartment of oral and maxillo-facial surgery, University Hospital Lyon Sud, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis report aims to present a case of temporomandibular joint (TMJ) ankylosis in a patient with Neurofibromatosis type 1 (NF1). It is a rare but significant long-term complication of NF1-associated craniofacial dysplasia, potentially aggravated by prior orthognathic surgery. CASE PRESENTATION: The patient, a 58-year-old woman with NF1 developed complete left TMJ ankylosis 14 years after bimaxillary surgery. The patient had a neurofibroma involving the mandibular branch (V3) of the trigeminal nerve, with fatty atrophy of the ipsilateral masticatory muscles. Clinical examination revealed marked facial asymmetry, severe trismus with a maximal mouth opening of 10 mm and tilting of the occlusal plane. Imaging studies confirmed ankylosis and extensive craniofacial bone dysplasia. Management was conducted in two surgical stages. The first involved resection of the ankylotic mass and placement of a temporary spacer. The second included orthognathic surgery and insertion of a custom-made TMJ prosthesis. Postoperative assessment showed improved mouth opening to 32 mm, with satisfactory aesthetic and functional outcomes.

conclusionNF1 is a genetic disorder characterized by a wide spectrum of systemic manifestations, including craniofacial skeletal anomalies. Although mandibular deformities are commonly observed in patients with facial plexiform neurofibromas, TMJ ankylosis is a rare and poorly documented complication. It underscores the need for individualized surgical planning and long-term surveillance in NF1 patients with facial neurofibromas and skeletal deformities. Clinicians should maintain a high index of suspicion for progressive joint pathology in NF1 patients. Early recognition and proactive management are essential to prevent irreversible joint damage. To our knowledge, this represents the first documented case of true TMJ ankylosis associated with NF1, confirmed both radiologically and surgically. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

AnkylosisNeurofibromatosis 1Orthognathic Surgical ProceduresPostoperative ComplicationsTemporomandibular Joint DisordersFemaleHumansMiddle AgedCraniofacial bone alterationsNeurofibromatosis 1NF-1Orthognathic surgeryTemporomandibular joint ankylosis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.