Case Report: Surgical Management of Compound Odontoma Associated With Unerupted Tooth
Case Report: Surgical Management of Compound Odontoma Associated With Unerupted Tooth
Case Report: Surgical Management of Compound Odontoma Associated With Unerupted Tooth
Case Report
Surgical Management of Compound Odontoma Associated with
Unerupted Tooth
Andrea Pacifici, Daniele Carbone, Roberta Marini, and Luciano Pacifici
Department of Oral and Maxillofacial Sciences, Sapienza University of Rome, Via Caserta 6, 00161 Rome, Italy
Correspondence should be addressed to Roberta Marini; [email protected]
Received 4 May 2015; Accepted 15 June 2015
Academic Editor: Junichi Asaumi
Copyright 2015 Andrea Pacifici et al. This is an open access article distributed under the Creative Commons Attribution License,
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Odontomas represent the most common type of odontogenic benign jaws tumors among patients younger than 20 years of
age. These tumors are composed of enamel, dentine, cementum, and pulp tissue. According to the World Health Organization
classification, two distinct types of odontomas are acknowledged: complex and compound odontoma. In complex odontomas, all
dental tissues are formed, but appeared without an organized structure. In compound odontomas, all dental tissues are arranged in
numerous tooth-like structures known as denticles. Compound odontomas are often associated with impacted adjacent permanent
teeth and their surgical removal represents the best therapeutic option. A case of a 20-year-old male patient with a compound
odontoma-associated of impacted maxillary canine is presented. A minimally invasive surgical technique is adopted to remove the
least amount of bone tissue as far as possible.
1. Introduction
According to the 2005 World Health Organization classification, odontoma is an odontogenic benign tumor of the young
age [1]. Despite this, odontomas are clinically considered
as tumor-like formations (hamartomas of dental tissues)
or developmental anomalies, rather than true odontogenic
neoplasms [2]. Two main types of odontoma are described:
(a) complex odontoma, an amorphous and disorderly pattern
of calcified dental tissues, and (b) compound odontoma, multiple miniature or rudimentary teeth [37]. The compound
odontoma has predilection toward the anterior maxilla (61%),
whereas only 34% of complex odontomas occur in this area;
the complex type shows a predilection for the posterior jaws
(59%) and lastly the premolar area (7%). Both variants are
made of all dental tissues such as enamel, dentin, cementum,
and pulp [7, 8].
Compound odontomas have numerous tooth-like structures (with altered size and shape) known as denticles.
At X-ray evaluation, compound odontomas appear as well
delimited lesions with a radiotransparent halo containing
radiodense zones which represent small denticles, separated
by fibrous septae, while in the complex types the radiodense
elements appear as irregular and disorderly masses with no
2. Case Description
A 20-year-old male patient in apparently good health conditions was referred to the Odontostomatological Clinic Unit,
Department of Oral and Maxillofacial Sciences (Sapienza
University of Rome, Italy), by his orthodontist for the absence
of the right upper permanent canine. The subject had no
significant medical history and had not reported oral trauma
(a)
(b)
3. Discussion
The term odontoma was introduced by Paul Broca in 1867 to
describe tumors formed by the overgrowth of transitory or
complete dental tissues. Odontomas are intraosseous lesions
mainly located in the anterior maxilla and anterior mandible,
although lesions localized in gingival soft tissues have also
been reported [7, 16]. The majority of odontomas are asymptomatic, although swelling, pain, suppuration, bony expansion, and displacement of teeth have been rarely observed.
Their pathogenesis has been associated with a number of
causes including trauma during primary dentition [9, 17],
hereditary anomalies such as Gardners syndrome, Hermanns syndrome, and basal cell nervous syndrome, odontoblastic hyperactivity, or alterations of the genetic components responsible for controlling dental development [8, 16].
(a)
(b)
(a)
(b)
Consent
Written informed consent was obtained from the patients
parents for publication of this case report and any accompanying images.
Conflict of Interests
The authors declare that they have no competing interests.
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