
Background
McCune-Albright syndrome (MAS) is a rare multisystem disorder characterized by the triad of polyostotic fibrous dysplasia (FD), endocrine disorders, and café-au-lait skin pigmentation. 90% of MAS patients have FD lesions in the craniofacial area, resulting in significant orofacial deformity, malocclusion, dental disorders, bone pain, and compromised oral health. Osteonecrosis of the jaw (ONJ) has recently been described as an adverse side effect of bisphosphonate therapy and is often correlated to infections or injury of the oral cavity.
Aim
The aim of the study is to investigate evidence of clinical and/or radiological signs of ONJ in FD/MAS pediatric patients due to bisphosphonate therapy.
Study design
13 FD/MAS patients (6 males and 7 females, aged 7 to 27 years, mean age 20 years and 4 months) were enrolled in the study. All patients during pediatric age have been treated with 1mg/kg/day pamidronate infusion for three days at 4–6 months intervals for an overall period of 30 months. All patients underwent medical investigation and complete extra-oral and intra-oral clinical examination to detect soft tissues swelling, dental caries, tooth mobility, malocclusion, bone exposure and/or fistulas. Ortopantomography, CT and/or MR imaging were evaluated in all cases.
Results
No patient developed ONJ. Dental eruption was normal in all cases and only three patients were treated for dental caries. None of them showed tooth mobility, bone exposure or fistulas or radiological signs different from jaw FD such as radiolucent cystic areas with a thin cortex. The major phenotypic expression of MAS was malocclusion (4 patients).
Conclusion
In spite of the low number of patients enrolled, results confirm that, in this population, ONJ can be ruled out as a chronic adverse side effect of bisphosphonate therapy. Good oral hygiene, careful dental care and follow-up are highly recommended in these patients.
References
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