Osteoma of the Jaw as First Clinical Sign of Gardner’s Syndrome: The Experience of Two Italian Centers and Review

Author:

D’Agostino Silvia1ORCID,Dell’Olio Fabio2ORCID,Tempesta Angela2ORCID,Cervinara Francesca2,D’Amati Antonio3ORCID,Dolci Marco1,Favia Gianfranco2,Capodiferro Saverio2ORCID,Limongelli Luisa2ORCID

Affiliation:

1. Department of Medical, Oral, and Biotechnological Sciences, University G. d’Annunzio, 66100 Chieti, Italy

2. Complex Operating Unit of Odontostomatology, Department of Interdisciplinary Medicine, Aldo Moro University, 70121 Bari, Italy

3. Operating Unit of Pathological Anatomy, Department of Emergency and Organ Transplantation, Aldo Moro University, 70121 Bari, Italy

Abstract

Gardner’s syndrome (GS) is a combination of polyposis, osteomas, fibromas, and sebaceous cysts. The aim of the study is to highlight whether maxillofacial osteoma could represent an early detection symptom of GS. Patients with suspected osteoma of the jaw underwent genetic and radiographical examinations. The database gathered 19 patients with oral osteoma that was histologically diagnosed; the whole sample was positive for APC gene mutation. Other cranial and peripheral locations were reported. Osteoma of the jaw is a crucial predictive factor of GS, and dentists and oral and maxillofacial surgeons must be aware of the importance of a timely diagnosis.

Publisher

MDPI AG

Subject

General Medicine

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