Volume 18, Issue 1 pp. 80-87
CASE REPORT

Calcifying epithelial odontogenic tumour with an atypical clinical presentation in a paediatric patient: A case report and literature review

Kelly dos Anjos Melo Pereira

Kelly dos Anjos Melo Pereira

University Hospital, Federal University of Juiz de Fora, Juiz de Fora, Brazil

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Daniel Amaral Alves Marlière

Corresponding Author

Daniel Amaral Alves Marlière

University Hospital, Federal University of Juiz de Fora, Juiz de Fora, Brazil

School of Dentistry, Federal University of Juiz de Fora, Juiz de Fora, Brazil

Correspondence

Daniel Amaral Alves Marlière, University Hospital of Federal University of Juiz de Fora (HU-UFJF/EBSERH), Av. Eugênio do Nascimento, Dom Bosco, Juiz de Fora, Minas Gerais 36038-330, Brazil.

Email: [email protected]

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Yuri de Lima Medeiros

Yuri de Lima Medeiros

Department of Stomatology, School of Dentistry, São Paulo University, São Paulo, Brazil

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Bruno Romano de Oliveira

Bruno Romano de Oliveira

School of Dentistry, Federal University of Juiz de Fora, Juiz de Fora, Brazil

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Fabio Ramôa Pires

Fabio Ramôa Pires

Oral Pathology, Dental School, Rio de Janeiro State University, Rio de Janeiro, Brazil

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First published: 02 October 2024

Abstract

Aim

We report a rare case of a calcifying epithelial odontogenic tumour with atypical clinical presentation in an adolescent and present a literature review of this tumour in paediatric patients.

Materials and Methods

A 12-year-old female patient presented with a painless swelling of the left mandible, with a history of 6 months. Clinical examination revealed a sessile mass with a reddish-pink colour and firm consistency. Tomographic images showed a hypodense, unilocular lesion involving unerupted tooth #34, with a hyperdense focus in contact with the tooth crown disrupting the buccal cortex.

Results

Enucleation, curettage and peripheral osteotomy of the lesion were performed, and the impacted tooth was removed, followed by the application of autologous leucocyte and platelet-rich fibrin matrices to the region. The patient evolved favourably with good clinical healing and evidence of new bone formation.

Conclusions

Despite its aggressive potential, the conservative approach for CEOT in paediatric patients proved to be effective. Our review found reports of recurrence up to 13 years after surgery. Therefore, long-term clinical and radiographical follow-up is indicated.

CONFLICT OF INTEREST STATEMENT

The authors declare that they have no known competing financial interests or personal relationships which could have appeared to influence the work reported in this article.

DATA AVAILABILITY STATEMENT

The datasets generated during and/or analysed during this study are available from the corresponding author on reasonable request.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.