Complex and Compound Odontomas

Boffano, Paolo; Zavattero, Emanuele; Roccia, Fabio; Gallesio, Cesare

doi:10.1097/scs.0b013e31824dba1f

Cited by 45 publications

(65 citation statements)

References 18 publications

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“…Not rare, the patient search for dental assistance due to the lack of eruption of a permanent tooth. Because the majority of odontomas are asymptomatic, and seldom causes swelling, pain, suppuration and/or bone expansion, this kind of tumour use to be discovered accidentally, after routine radiograph examination 7 13 15. In general, odontomas causes the impaction of permanent teeth as presented in this case, but sometimes they can be associated with primary dentition 10–13…”

Section: Discussionmentioning

confidence: 90%

“…It has been suggested that the odontoma, once enucleated, usually does not recur in young children, but a close follow-up is needed 11. If odontomas are extirpated early without disturbing the underlying tooth germ, the eruption of the impacted tooth can be expected spontaneously 7 16. In a retrospective investigation of 73 cases of odontomas, 53.2% of the impacted teeth erupted after the surgical removal of the odontogenic tumours 15.…”

Section: Discussionmentioning

confidence: 99%

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Impacted permanent incisors associated with compound odontoma

Machado

Knop

Rocha³

et al. 2015

BMJ Case Reports

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Odontomas are the most common odontogenic tumours of the maxillary bones, characterised by a slow growth and benign behaviour. They are usually small, asymptomatic and diagnosed after routine radiographic examination. The aim of this study was to report a case of a compound odontoma in the anterior maxilla of a 7-year-old girl, which was causing the impaction of the maxillary right central and lateral incisors, as well as the prolonged retention of the corresponding primary teeth. We also aimed to review the literature about these tumours, since they are not part of the dentist's day-to-day clinical practice. The clinical and radiographic features, the diagnosis and treatment of the case were discussed in this work.

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Section: Discussionmentioning

confidence: 90%

Section: Discussionmentioning

confidence: 99%

Impacted permanent incisors associated with compound odontoma

Machado

Knop

Rocha³

et al. 2015

BMJ Case Reports

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“…Si no aparecen signos ni síntomas, esta lesión puede permanecer en el hueso muchos años sin producir manifestaciones clínicas, tales como formación de quistes dentígenos o quiste odontogénico epitelial calcificante (Fernandes et al, 2005). El tratamiento de elección para estos casos es la enucleación simple de la lesión, siendo un tratamiento conservador (Boffano et al, 2012).…”

Section: Discussionunclassified

Queratoquiste Odontogénico en un Paciente con Displasia Cleidocraneal: Reporte de un Caso

Martinovic-Guzmán

Vergara-Iturriaga

Alister-Herdener

et al. 2019

Int. J. Odontostomat.

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MARTINOVIC, G. G.; VERGARA, M. I.; ALISTER, J. P. H. & MANTEROLA, C. Queratoquiste odontogénico en un paciente con displasia cleidocraneal: Reporte de un caso. Int. J. Odontostomat., 13(2):189-194, 2019. RESUMEN:La displasia cleidocraneal (DCC), es un trastorno autosómico dominante poco común, que involucra principalmente a los huesos que se osifican por vía membranosa; afectando el cierre de fontanelas craneales y el desarrollo de las clavículas, además de anomalías dentales y vertebrales. El objetivo de este manuscrito fue reportar el caso de una paciente con DCC que presentó un queratoquiste odontogénico (QQO) intrasinusal. Presentamos el caso de una paciente de 81 años, diagnosticada en su niñez con DDC, que consultó por un desajuste protésico y molestias en relación a la zona del seno maxilar derecho. Clínicamente se observó desajuste de la prótesis y aumento de volumen de márgenes poco definidos en la zona maxilar derecha, color rosa coral; que se extendía por todo el margen hemimaxilar derecho hasta el fondo de vestíbulo; doloroso a la palpación, con un mes de evolución. Se solicitó CBCT, con el que se pudo verificar la presencia de un desarrollo tumoral de contenido similar a dentículos, ubicado en la totalidad del seno maxilar derecho; extendiéndose hasta el piso de la cavidad nasal y orbitaria. Se estableció la hipótesis diagnóstica de "odontoma compuesto". Se le intervino quirúrgicamente, bajo anestesia general, realizándose una excisión de la lesión; la que era de márgenes definidos, con cambios de coloración en tonos oscuros, con la inclusión de tres piezas dentarias; de aspecto maligno. Se logró enucleación completa, dejando remanente óseo limpio. La pieza fue enviada a estudio histopatológico. En informe histopatológico, describió la presencia de una lesion quistica con pared compatible con queratoquiste.PALABRAS CLAVE: displasia cleidocraneal, queratoquiste, dientes supernumerarios.

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“…Complex odontomas are more prevalent than compound odontomas 12. The aetiology of odontomas is due to gene mutations or interference, or possibly postnatal genetic control of odontogenesis.…”

Section: Discussionmentioning

confidence: 99%

Bilateral coronoid hypoplasia and complex odontoma: a rare concurrence of developmental pathology and odontogenic tumour of the mandible

et al. 2015

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SUMMARYWe present a rare case of concurrent bilateral coronoid hypoplasia and complex odontoma in the mandible, with replacement of missing posterior teeth in both sides of the lower jaw. A 20-year-old woman was diagnosed with bilateral occurrence of coronoid hypoplasia and unerupted complex odontoma after radiographic and histopathological examination. The patient was surgically treated with complete removal of the unerupted complex odontoma and prosthetic replacement of the missing teeth. BACKGROUND

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Complex and Compound Odontomas

Cited by 45 publications

References 18 publications

Impacted permanent incisors associated with compound odontoma

Impacted permanent incisors associated with compound odontoma

Queratoquiste Odontogénico en un Paciente con Displasia Cleidocraneal: Reporte de un Caso

Bilateral coronoid hypoplasia and complex odontoma: a rare concurrence of developmental pathology and odontogenic tumour of the mandible

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