Sequelae of congenital oropharyngeal teratoma in the oral cavity of the child

case report

Authors

  • Letícia Bruno Qualhato Federal University of Uberlândia
  • Ana Carolina Candelas Peixoto Federal University of Uberlândia
  • Késia Lara dos Santos Marques Federal University of Uberlândia
  • Celia Regina Moreira Lanza Federal University of Uberlândia
  • Luiz Roberto da Silva Federal University of Uberlândia
  • Guilherme Silva de Mendonça Hospital de Clínicas da Universidade Federal de Uberlândia https://orcid.org/0000-0001-5635-2708
  • Fabiana Sodré de Oliveira Federal University of Uberlândia

DOI:

https://doi.org/10.31686/ijier.vol9.iss7.3225

Keywords:

Teratoma, Oropharynx, Child, Preschool, Oral Cavity, Case Reports

Abstract

Congenital oropharyngeal teratoma is a rare tumor subtype with cells from the three germ layers, majorly being benign. Whereas teratoma develops early in intrauterine life, thus affecting the growth and development of adjacent structures, the purpose of this case report is to present the sequelae of this tumor in a child's oral cavity. Female child, 2 years and 3 months old referred by the otorhinolaryngologist for dental evaluation. The mother´s main complaint was the the child could not close her mouth. According to the child's medical record, at 34th week of gestation, during the routine ultrasound examination, the presence of the anechoic tumor mass was observed without Doppler signal, presenting a 3.2cm x 2.4cm diameter outside through the oral cavity. At 17 and 32 days of life, respectively, the excision of the largest and residual tumor located on the floor of the mouth was performed. Upon anatomopathological examination, the tumor with was classified as a mature teratoma. In the intraoral examination, a deep and atresia palate incomplete cleft palate, bone growth in the region of the posterior alveolar ridge of the maxilla, and in the posterior region of the mandible on the left side, "V" shaped mandible and microglossia, crowding were observed dental agenesis of the lower lateral incisors, absence of caries lesions, gingivitis and enamel development defects. The child will remain under the regular dental pediatric follow-up. Several sequelae were observed in the child's oral cavity and the need for multi-professional follow-up after excision of congenital oropharyngeal teratoma.

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Author Biographies

  • Letícia Bruno Qualhato, Federal University of Uberlândia

    Graduated from the Dentistry Course, Faculty of Dentistry, Federal University of Uberlândia

    Uberlândia, Minas Gerais, Brazil.

  • Ana Carolina Candelas Peixoto, Federal University of Uberlândia

    Student of the Dentistry Course, Faculty of Dentistry, Federal University of Uberlândia.

    Uberlândia, Minas Gerais, Brazil.

  • Késia Lara dos Santos Marques, Federal University of Uberlândia

    Dental surgeon of the Special Patients Sector at the Dental Hospital of the Federal University of Uberlândia.

    Uberlândia, Minas Gerais, Brazil.

  • Celia Regina Moreira Lanza, Federal University of Uberlândia

    Professor in the Department of Clinic, Pathology and Dental Surgery, Faculty of Dentistry, Federal University of Minas Gerais.

    Uberlândia, Minas Gerais, Brazil.

  • Luiz Roberto da Silva, Federal University of Uberlândia

    Master in Genetic-Clinical Study in Mental Disability. Pediatric Physician Hospital de Clínicas, Federal University of Uberlândia.

    Uberlândia, Minas Gerais, Brazil.

  • Fabiana Sodré de Oliveira, Federal University of Uberlândia

    Professor of Pediatric Dentistry, Faculty of Dentistry, Federal University of Uberlândia.

    Uberlândia, Minas Gerais, Brazil.

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Published

2021-07-01

How to Cite

Qualhato, L. B. ., Peixoto, A. C. C. ., Marques, K. L. dos S. ., Lanza, C. R. M. ., Silva, L. R. da ., Mendonça, G. S. de, & Oliveira, F. S. de . (2021). Sequelae of congenital oropharyngeal teratoma in the oral cavity of the child: case report. International Journal for Innovation Education and Research, 9(7), 173-183. https://doi.org/10.31686/ijier.vol9.iss7.3225
Received 2021-06-01
Accepted 2021-06-29
Published 2021-07-01