Produção Nacional
Revisado por pares
Gardner Syndrome With Unusual Maxillofacial Manifestation
2016; Lippincott Williams & Wilkins; Volume: 27; Issue: 5 Linguagem: Inglês
10.1097/scs.0000000000002741
ISSN1536-3732
AutoresMarina Reis Oliveira, Willian Caetano Rodrigues, Mário Francisco Real Gabrielli, Marisa Aparecida Cabrini Gabrielli, Mirian Aparecida Onofre, Valfrido Antônio Pereira Filho,
Tópico(s)Oral and Maxillofacial Pathology
ResumoGardner syndrome is a rare autosomal-dominant condition characterized by the presence of intestinal polyposis, multiple osteomas, and tumors of the hard and soft tissues. This paper describes a patient of Gardner syndrome with unusual maxillofacial manifestation with presence of fibromyxomatous injury in jaw, coronoid hyperplasia, and multiple osteomas diffusely distributed in the craniomaxillofacial skeleton. Imaging examinations have identified craniofacial manifestations and the patient was referred to the gastroenterologist who confirmed the diagnosis of Gardner syndrome. The early diagnosis of this syndrome is important since intestinal polyps have high potential for malignant transformation. It is therefore essential that dentists are familiar with the maxillofacial features of this condition, since they precede the intestinal polyposis and encourage early diagnosis. In addition to classic maxillofacial signs of this syndrome, one must consider that, although it is rare, other injuries may be present such as those described in this clinical patient.
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