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A Rare Case of Peripheral Osteoma of the Alveolar Bone of the Maxilla in a 13-Year-Old Boy.
J Clin Med
November 2024
Department of Dental Medicine, Faculty of Medicine, University of Novi Sad, Hajduk Veljkova 3, 21000 Novi Sad, Serbia.
This report aims to augment the presently limited knowledge on the characteristics of jawbone osteomas in children by presenting an exceptionally rare case of this tumor located on the buccal aspect of the alveolar process of the maxilla in a 13-year-old boy. A well-defined, painless, bony, hard, spherical enlargement on the maxillary alveolar ridge was identified and thoroughly evaluated through clinical examination, panoramic radiographs, CBCT (Cone Beam Computed Tomography) scans, and histopathological analysis. The tumor was surgically removed, and the patient participated in postoperative clinical follow-ups for eight years.
View Article and Find Full Text PDFLarge Peripheral Osteomas and Dental Implants: A Case Report.
Medicina (Kaunas)
July 2024
Department of Periodontology, College of Dentistry, Kyung Hee University Dental Hospital, Kyung Hee University, Seoul 02447, Republic of Korea.
Article Synopsis
- Peripheral osteoma of the jaw is a rare and benign growth that typically appears as a single, slow-growing mass; cases of multiple osteomas without related syndromes are even rarer.
- A 75-year-old patient developed several of these masses in the jaw after dental implants were placed, making oral hygiene difficult.
- Surgical removal of the osteomas improved the patient's chewing function and oral health, with no recurrence noted after one year, suggesting that dental implants may influence the slow growth of these lesions.
Osteoblastoma and Osteoid Osteoma of the Mandible: Review of the Literature and Report of Two Cases.
Case Rep Dent
March 2022
Department of Oral Medicine, School of Dentistry, University of Washington, Box 356370, 1959 NE Pacific St, Seattle, WA 98195, USA.
Osteoblastoma and osteoid osteoma are rare benign neoplasms of the jaws. We reviewed current literature surrounding the ongoing debate over similarities and differences of osteoblastoma and osteoid osteoma and present two cases. Both cases are well-demarcated mixed radiodensity mandibular lesions with histological features of osteoblastoma.
View Article and Find Full Text PDFIdentification of aggressive Gardner syndrome phenotype associated with a de novo variant, c.4666dup.
Cold Spring Harb Mol Case Stud
April 2019
Departments of Otorhinolaryngology, Head and Neck Surgery, USA.
Gardner syndrome describes a variant phenotype of familial adenomatous polyposis (FAP), primarily characterized by extracolonic lesions including osteomas, dental abnormalities, epidermal cysts, and soft tissue tumors. We describe a 2-yr-old boy presenting with a 2-cm soft tissue mass of the forehead. Pathologic evaluation revealed a nuchal-type/Gardner-associated fibroma.
View Article and Find Full Text PDFA case of multiple osseous choristomas arising on the medial side of the lateral pterygoid muscle.
Oral Radiol
January 2019
Department of Dentistry, Oral and Maxillofacial-Plastic and Reconstructive Surgery, Faculty of Medicine, Yamagata University, 2-2-2 Iidanishi, Yamagata, 990-9585, Japan.
Osseous choristoma is a rare entity in the oral and maxillofacial region. The most common site is the tongue, followed by the buccal mucosa. Osseous choristoma of the muscle is unusual and few cases have been described in the literature.
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