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1Cleft Lip and Palate-Craniomaxillofacial Unit, Hospital Nacional de Niños Dr. Carlos Sáenz Herrera, Caja Costarricense de Seguro Social, San José, Costa Rica
2Department of Diagnostic and Surgical Sciences, Universidad de Costa Rica, San José, Costa Rica
Osteoblastoma is a rare benign neoplasm formed by osteoid tissue and well-vascularized bone that occurs mainly in children and adolescents. It appears primarily in the long bones, vertebral column, and small bones of the hands and feet, and not typically in the skull and maxillary bones. The purpose of this study is to present the case of an 8-year-old girl with a diagnosis of right mandibular osteoblastoma and a review of the relevant literature.
The goals of treatment were to preserve dental occlusion, masticatory function and facial symmetry while minimizing the effects on patient body image and quality of life. Osteoblastoma, although it is benign, can be aggressive, and its treatment will depend on the timing of diagnosis, size and location.
Early diagnosis is essential to avoid not only radical surgery as in the case presented, but also to help minimize the risk of possible relapse and potential malignancy of a benign osteoblastoma.
Fig. 1
Right mandibular ramus osteoblastoma, extending from condyle and coronoid process to permanent lower right first molar: computed axial tomography (A and B: 3D reconstruction images, C: axial image, D: coronal image) and orthopantomography (E).
Fig. 2
Right mandibular ramus osteoblastoma. A. Tumor. B. Silicon spacer for reconstruction of right mandibular ramus. C. Silicon spacer positioned and fixed in mandible. D. Immediate postoperative radiographic control by orthopantomography.
Fig. 3
Patient monitoring images: computed axial tomography (A and B: 3D reconstruction images), two years postoperative, and orthopantomography (C), three years postoperative. Note on the radiograph, the right lower second premolar tooth, which erupted despite the absence of root formation.
Reference
References
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