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Ameloblastoma: a clinical and therapeutic analysis on six cases Please cite this article as: de Moraes FB, Cardoso RMN, Rodrigues SV, Dutra MVF, Pereira UR, Borges TRSA. Ameloblastoma: uma análise clínica e terapêutica de seis casos. Rev Bras Ortop. 2014;49:305-308. , ☆☆ ☆☆ Work performed in the Department of Orthopedics and Traumatology, Hospital das Clínicas, Universidade Federal de Goiás, Goiânia, GO, Brazil.

Abstracts

Ameloblastomas are odontogenic tumors that are locally invasive and slow-growing. Their etiology is still not well defined, but the forms of treatment have been widely discussed because of the possibility of tumor recurrence and postoperative complications. In this study, six patients who were diagnosed with ameloblastoma in the mandibular region and were treated in the Department of Orthopedics and Traumatology of Hospital das Clínicas, Federal University of Goiás, between 1958 and 1963, were evaluated. The radiological, clinical and therapeutic characteristics were evaluated. There was no predominance regarding gender in the sample studied. The symptoms most often presented by the patients were pain and tumor formation. The radiological characteristics with greatest incidence were multilocular lesions and the treatment used for all the patients was radical surgery. There was no recurrence over the minimum follow-up period of one year and six months.

Ameloblastoma/etiology; Ameloblastoma/diagnosis; Ameloblastoma/surgery; Mandibular neoplasms


Os ameloblastomas são tumores odontogênicos, localmente invasivos e de crescimento lento. Sua etiologia ainda não foi bem definida e as formas de tratamento são amplamente discutidas, por causa de possíveis recidivas do tumor e complicações pós-operatórias. Neste trabalho, foram avaliados seis pacientes diagnosticados com ameloblastoma na região mandibular e tratados no Departamento de Ortopedia e Traumatologia do HC-UFG, de 1958 a 1963. Foram avaliadas as características radiológicas, clínicas e terapêuticas. Não houve predomínio em relação ao gênero na amostra estudada. Os sintomas mais apresentados pelos pacientes foram dor e tumoração. As características radiológicas de maior incidência são de uma lesão multilocular e o tratamento usado em todos os pacientes foi o cirúrgico radical. A recidiva foi nula em um tempo mínimo de um ano e sete meses de seguimento.

Ameloblastoma/etiologia; Ameloblastoma/diagnóstico; Ameloblastoma/cirurgia; Neoplasias mandibulares


Introduction

Odontogenic tumors are neoplasms derived from the cells responsible for odontogenesis.11. Sá AC, Zardo M, Paes Júnior AJ, Souza RP, Neme MP, Sabedotti I, et al. Ameloblastoma da mandíbula: relato de dois casos. Radiol Bras. 2009;37(6):465-8. According to the tissue origin, they are classified as epithelial, mesodermal or mixed. Ameloblastomas are the commonest tumors of epithelial origin and account for around 23% of odontogenic tumors.22. Avelar RL, Antunes AA, Santos TS, Andrade ESS, Dourado E. Tumores odontogênicos: estudo clínico-patológico de 238 casos. Rev Bras Otorrinolaringol. 2008;74(5):668-73.

Ameloblastomas were first described by Cusack in 1827 apud Chagas et al.33. Chagas JF, Toledo Júnior JI, Pascoal MBN, Pascoal MI, Aquino JL, Campos JLG, et al. Ameloblastomas: aspectos clínicos e terapêuticos. Rev Bras Cir Cabeça Pescoç o. 2007;36(3):159-62. They are locally aggressive and highly infiltrative, and have a high recurrence rate that has been estimated to be around 50%. Despite these characteristics, they are neoplasms that only rarely undergo metastasis.44. Ciment LM, Ciment AJ. Malignant ameloblastoma metastatic to the lungs 29 years after primary resection. Chest. 2002;121(4):1359-61.

They are generally asymptomatic in their initial stages, which have the implication that they are only diagnosed later on, when the tumors have already reached a large size. The commonest symptoms are swelling, pain and local discomfort.33. Chagas JF, Toledo Júnior JI, Pascoal MBN, Pascoal MI, Aquino JL, Campos JLG, et al. Ameloblastomas: aspectos clínicos e terapêuticos. Rev Bras Cir Cabeça Pescoç o. 2007;36(3):159-62. and 55. Kim SG, Jang HS. Ameloblastoma: a clinical, radiographic, and histopathologic analysis of 71 cases. Oral Surg Oral Med Oral Pathol. 2001;91(6):649-53.

The objective of this study was to report on and discuss the clinical-radiological characteristics of six patients with ameloblastomas who were attended at Hospital das Clínicas, Federal University of Goiás (HC-UFG).

Methodology

The medical files of six patients who were attended in the Department of Orthopedics and Traumatology (DOT) of HC-UFG over a five-year period (1958-1963) were reviewed. This was therefore a retrospective descriptive study. All the information relating to age, sex, clinical manifestations, tumor location, time when the symptoms started, radiological characteristics, form of treatment, length of follow-up and recurrences was studied.

The locations were divided between the mandible and the maxilla and, for locations in the mandible, it was investigated whether the tumor affected the body, angle or ramus of the mandible, or some combination of these. According to the number of radiolucent compartments of the lesion, the tumors were classified as unilocular or multilocular; in the latter case, they would take on a "honeycomb" or "soap bubble" appearance.66. Swan JS. The teeth, jaws, and salivary glands. In: Juhl JH, Crummy AB, Kuhlman JE, editors. Paul & Juhl's essentials of radiologic imaging [versão digital]. 7th ed. Philadelphia: Lippincott Williams & Wilkins; 1998. p. 13-31. , 77. Ogunsalu C, Daisley H, Henry K, Bedayse S, White K, Jagdeo B, et al. A new radiological classification for ameloblastoma based on analysis of 19 cases. West Indian Med J. 2006;55(6):36-41. , 88. Martinez CR, Barros RM, Orué NR, Oliveira JGP, Monteiro JCC. Ameloblastoma: estudo clínico-histopatológico. Rev Cir Traumatol Buco-Maxilo-Fac. 2008;8(2):55-60. and 99. Martins MD, Rosa Junior OA, Martins MAT, Bussadori SK, Fernandes KPS. Ameloblastoma: revisão de literatura. ConScientia e Saúde. 2007;6(2):269-78. Disponível em: http://www4.uninove.br/ojs/index.php/saude/article/viewFile/ 1108/886
Disponível em: http://www4.uninove.br/oj...
The surgical treatment was classified as radical or non-radical. According to this division, treatment described as non-radical consisted of enucleation or curettage, while radical treatment consisted of complete or partial surgical resection of the tumor.1010. Gardner DG, Pecak AM. The treatment of ameloblastoma based on pathologic and anatomic principles. Câncer. 1980;46(11):2514-9.

Results

The group was composed of three men and three women. Their mean age was 37.5 years (range: 25-50). The tumor was located in the mandible in all the patients. Two cases involved only the body of the mandible; one, the body and angle; and two, the body, angle and ramus.

The commonest symptoms presented were complaints of increased mandibular volume, i.e. tumor growth and pain (spontaneous or during mastication), which were present in all the patients. Additional symptoms that were present in only two patients are: limitation of movement and formation of a fistula into the oral cavity with discharge of purulent and bloody content.

The time that had elapsed from the beginning of the symptoms to the consultation at HC-UFG ranged from one to eight years, for five patients who had not had any previous treatment. There was one specific case in which the symptoms started 24 years before the consultation in this hospital, but this was a differentiated case because the patient had already gone through two non-radical treatments (curettage), with tumor recurrence.

There were no descriptions of radiography in the medical files of the two patients. The radiographs available on the other patients had a multilocular appearance (Fig. 1). It could be seen in all the cases that these tumors had reached enormous sizes and were described in accordance with parameters used at that time, as presenting the size of a "lime" or of a "large orange". These measurements would be equivalent to approximately 4 cm × 5 cm × 5 cm for the smaller tumors and 8 cm × 8 cm × 9 cm for the larger tumors. This explains why the treatment used in all the cases was surgical resection of the tumor, i.e. radical treatment.

Fig.1
Before the operation.

Five patients were followed up after the surgical treatment. The length of follow-up ranged from one year and seven months to seven years and two months. None of these patients presented recurrence (Table 1 and Fig. 2).

Table 1
Clinical characteristics of the patients with ameloblastoma.

Fig.2
After the operation.

Discussion

The ratio between the sexes was 1:1 in this study. This is in accordance with the literature, in which it is usually shown that there is no notable relation to gender regarding occurrences of ameloblastoma.11. Sá AC, Zardo M, Paes Júnior AJ, Souza RP, Neme MP, Sabedotti I, et al. Ameloblastoma da mandíbula: relato de dois casos. Radiol Bras. 2009;37(6):465-8. , 33. Chagas JF, Toledo Júnior JI, Pascoal MBN, Pascoal MI, Aquino JL, Campos JLG, et al. Ameloblastomas: aspectos clínicos e terapêuticos. Rev Bras Cir Cabeça Pescoç o. 2007;36(3):159-62. , 88. Martinez CR, Barros RM, Orué NR, Oliveira JGP, Monteiro JCC. Ameloblastoma: estudo clínico-histopatológico. Rev Cir Traumatol Buco-Maxilo-Fac. 2008;8(2):55-60. , 1111. Martins RH, Andrade J, Sobrinho, Rapoport A, Rosa MP. Histopathologic features and management of ameloblastoma: study of 20 cases. São Paulo Med J. 1999;117(4):171-4. and 1212. Costa DO, Ecard MB, Oliveira SP, Silva LE, Dias EP, Lourenço SQC. Estudo retrospectivo dos casos diagnosticados como ameloblastoma no Serviço de Anatomia Patológica do Hospital Universitário Antônio Pedro entre 1997 e 2007. J Bras Patol Med Lab. 2008;44(6):441-7. In a study conducted on 116 patients, the ratio between the male and female genders was 1.2:1,55. Kim SG, Jang HS. Ameloblastoma: a clinical, radiographic, and histopathologic analysis of 71 cases. Oral Surg Oral Med Oral Pathol. 2001;91(6):649-53. and a single study in which this ratio was analyzed found that it was 2:1, with predominance among males.1313. Lagares DT, Cossío PI, Guisado JMH, Pérez JL. Mandibular ameloblastoma. A review of the literature and presentation of six cases. Med Oral Patol Oral Cir Bucal. 2004;10(3):231-8.

Regarding the patients' ages, the mean was 37.5 years. This is also confirmed in the literature, where these tumors have been shown to be predominantly in adults, generally in their fourth or fifth decade of life.33. Chagas JF, Toledo Júnior JI, Pascoal MBN, Pascoal MI, Aquino JL, Campos JLG, et al. Ameloblastomas: aspectos clínicos e terapêuticos. Rev Bras Cir Cabeça Pescoç o. 2007;36(3):159-62. and 1212. Costa DO, Ecard MB, Oliveira SP, Silva LE, Dias EP, Lourenço SQC. Estudo retrospectivo dos casos diagnosticados como ameloblastoma no Serviço de Anatomia Patológica do Hospital Universitário Antônio Pedro entre 1997 e 2007. J Bras Patol Med Lab. 2008;44(6):441-7.

Ameloblastomas have been found located in the mandible in around 80% of the cases and in the maxilla in the remaining 20%.33. Chagas JF, Toledo Júnior JI, Pascoal MBN, Pascoal MI, Aquino JL, Campos JLG, et al. Ameloblastomas: aspectos clínicos e terapêuticos. Rev Bras Cir Cabeça Pescoç o. 2007;36(3):159-62. , 88. Martinez CR, Barros RM, Orué NR, Oliveira JGP, Monteiro JCC. Ameloblastoma: estudo clínico-histopatológico. Rev Cir Traumatol Buco-Maxilo-Fac. 2008;8(2):55-60. , 1111. Martins RH, Andrade J, Sobrinho, Rapoport A, Rosa MP. Histopathologic features and management of ameloblastoma: study of 20 cases. São Paulo Med J. 1999;117(4):171-4. , 1212. Costa DO, Ecard MB, Oliveira SP, Silva LE, Dias EP, Lourenço SQC. Estudo retrospectivo dos casos diagnosticados como ameloblastoma no Serviço de Anatomia Patológica do Hospital Universitário Antônio Pedro entre 1997 e 2007. J Bras Patol Med Lab. 2008;44(6):441-7. and 1414. Medeiros M, Porto GG, Laureano Filho JR, Portela L, Vasconcellos RH. Ameloblastoma em mandíbula. Rev Bras Otorrinolaringol. 2008;74(3):478. In our study, all of them were located in the mandible, and this is close to the data found by Kim and Jang,55. Kim SG, Jang HS. Ameloblastoma: a clinical, radiographic, and histopathologic analysis of 71 cases. Oral Surg Oral Med Oral Pathol. 2001;91(6):649-53. who in a study on 71 cases observed occurrences of ameloblastomas in the mandible in 93.9% of them. In the same study, the location was only in the body of the mandible in 60.6% of the cases and in the body and angle in 2.8% of the cases, while there were no cases located simultaneously in the body, angle and ramus of the mandible.55. Kim SG, Jang HS. Ameloblastoma: a clinical, radiographic, and histopathologic analysis of 71 cases. Oral Surg Oral Med Oral Pathol. 2001;91(6):649-53. Tumors that are more voluminous may affect the adjacent soft tissues in an infiltrative manner, to the point of promoting erosion and reabsorption of the tooth roots.11. Sá AC, Zardo M, Paes Júnior AJ, Souza RP, Neme MP, Sabedotti I, et al. Ameloblastoma da mandíbula: relato de dois casos. Radiol Bras. 2009;37(6):465-8.

Our sample included two cases in which only the body of the mandible was affected; one, the body and angle; and two, the body, angle and ramus. This was probably due to the long period of evolution. The tumors had already reached large proportions, which thus explains why the body, angle and ramus were simultaneously affected, which had not been reported in other studies.

The clinical manifestations most commonly presented by the patients were tumor growth (100%) and pain (100%), followed by limitations on movement (33.3%) and formation of fistulas with drainage of pus and/or blood (33.3%). The authors of the studies analyzed are unanimous in stating that the vast majority of ameloblastomas are slow growing and therefore only rarely manifest with signs other than local tumor growth, which is the commonest finding.33. Chagas JF, Toledo Júnior JI, Pascoal MBN, Pascoal MI, Aquino JL, Campos JLG, et al. Ameloblastomas: aspectos clínicos e terapêuticos. Rev Bras Cir Cabeça Pescoç o. 2007;36(3):159-62. , 55. Kim SG, Jang HS. Ameloblastoma: a clinical, radiographic, and histopathologic analysis of 71 cases. Oral Surg Oral Med Oral Pathol. 2001;91(6):649-53. and 1313. Lagares DT, Cossío PI, Guisado JMH, Pérez JL. Mandibular ameloblastoma. A review of the literature and presentation of six cases. Med Oral Patol Oral Cir Bucal. 2004;10(3):231-8. Medeiros et al.1414. Medeiros M, Porto GG, Laureano Filho JR, Portela L, Vasconcellos RH. Ameloblastoma em mandíbula. Rev Bras Otorrinolaringol. 2008;74(3):478. also cited Neville et al.1616. Neville BW, Damm DD, Allen CM, Bouquot JE. Patologia oral & maxilofacial. 2nd ed. Rio de Janeiro: Guanabara; 2004. to affirm that these tumors are only rarely painful, unless they become secondarily infected, and that signs or symptoms of nerve impairment are uncommon, even in large tumors. Thus, the high prevalence of pain in the cases reported may be indicative of associated infectious processes, particularly when it is taken into consideration that in some cases there was a great hiatus of time between the beginning of the symptoms and seeking medical assistance.

The characteristic most commonly found through radiographic analysis is the multilocular pattern (65.4%), as shown in the study on 52 cases by Saddy et al.1515. Saddy MS, Chilvarquer I, Dib LL, Sandoval RL. Aspectos clínicos, radiográficos e terapêuticos do ameloblastoma. Rev Pós Grad. 2005;12(4):460-5. Disponível em: http://www.fo.usp.br/revistas/rpg/EDICOES/RPG-4 09 684.pdf
Disponível em: http://www.fo.usp.br/revi...
In our study, the multilocular pattern also predominated. However, even with a clearly determined radiographic appearance, the definitive diagnosis of ameloblastoma should be sought by correlating this with histopathological examination of the lesion.33. Chagas JF, Toledo Júnior JI, Pascoal MBN, Pascoal MI, Aquino JL, Campos JLG, et al. Ameloblastomas: aspectos clínicos e terapêuticos. Rev Bras Cir Cabeça Pescoç o. 2007;36(3):159-62.

Regarding the histopathological pattern, three types of tumor can be differentiated: solid or multicystic, unicystic and peripheral. The multicystic form accounts for around 85% of the cases; it is locally invasive and presents large numbers of recurrences. The unicystic form accounts for around 14% of the cases; it is less invasive and does not present large numbers of recurrences. The peripheral form is rare, accounting for less than 1% of the cases, and it only affects soft tissues surrounding the region of the teeth.1616. Neville BW, Damm DD, Allen CM, Bouquot JE. Patologia oral & maxilofacial. 2nd ed. Rio de Janeiro: Guanabara; 2004.

Ameloblastomas present only a few symptoms at a late stage, which makes it difficult to identify these tumors at their early stages.99. Martins MD, Rosa Junior OA, Martins MAT, Bussadori SK, Fernandes KPS. Ameloblastoma: revisão de literatura. ConScientia e Saúde. 2007;6(2):269-78. Disponível em: http://www4.uninove.br/ojs/index.php/saude/article/viewFile/ 1108/886
Disponível em: http://www4.uninove.br/oj...
It has been shown that when individuals realize that they have this tumor, or a healthcare professional notices it, the tumor already presents a considerable volume. Another obstacle is that in many cases, the patients perceive the tumor growth as having the consistency of bone, but end up seeking medical care only after the condition has evolved for some time, which may even be years later. In this case series, all the patients were individuals of low social class and had difficulties in accessing healthcare services. For this reason, these tumors had evolved over a longer time and therefore had large dimensions. It has been reported that infiltration of adjacent soft tissues may occur in cases of tumors that are more voluminous.11. Sá AC, Zardo M, Paes Júnior AJ, Souza RP, Neme MP, Sabedotti I, et al. Ameloblastoma da mandíbula: relato de dois casos. Radiol Bras. 2009;37(6):465-8. One of these cases had even evolved from the beginning of the symptoms eight years earlier and was the one with the greatest tumor growth in terms of dimensions, comparable with the size of a large avocado.

The treatment for ameloblastomas is surgical and may be radical or non-radical. Radiotherapy is not indicated, since the lesions are radioresistant. Non-radical treatment is generally used for unicystic tumors. However, according to Nakamura et al.,1717. Nakamura N, Higuchi Y, Mitsuyasu T, Sandra F, Ohishi M. Comparison of long-term results between different approaches to ameloblastoma. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2002;93(1):13-20. this treatment method, which includes marsupialization and enucleation followed by appropriate bone curettage, has been shown to be very efficient and has reduced the need for surgical resection and thus reinforced the indications for non-radical treatment for ameloblastomas.

In turn, radical treatment implies total removal of the lesion, generally with a safety margin of one to two centimeters,1 1. Sá AC, Zardo M, Paes Júnior AJ, Souza RP, Neme MP, Sabedotti I, et al. Ameloblastoma da mandíbula: relato de dois casos. Radiol Bras. 2009;37(6):465-8. and 1313. Lagares DT, Cossío PI, Guisado JMH, Pérez JL. Mandibular ameloblastoma. A review of the literature and presentation of six cases. Med Oral Patol Oral Cir Bucal. 2004;10(3):231-8. and is more indicated for lesions that are more aggressive, such as in cases of multicystic ameloblastoma or even in unicystic cases with infiltrating characteristics. In our cases, we chose radical surgical treatment for all the patients mainly because of their late diagnosis, with tumors that already had large dimensions. In this case series, radical therapeutic management did not present recurrence in the five cases that were followed up. One of these cases had even presented recurrences subsequent to curettage performed previously at another service.

Regarding the length of follow-up, our cases did not show any recurrence over a minimum period of one year and seven months. However, it should be taken into consideration that two of the cases were followed up for less than three years. Most studies have evaluated recurrence over a mean period of four to five years.1313. Lagares DT, Cossío PI, Guisado JMH, Pérez JL. Mandibular ameloblastoma. A review of the literature and presentation of six cases. Med Oral Patol Oral Cir Bucal. 2004;10(3):231-8. Nevertheless, since all of our cases were treated with full surgical resection and with a mean length of follow-up of four years and seven months, i.e. concordant with other studies,1818. Olaitan AA, Arole G, Adekeye EO. Recurrent ameloblastoma of the jaws: a follow-up study. Int J Oral Maxillofac Surg. 1998;27(6):456-60. and 1919. Olaitan AA, Adekeye EO. Unicystic ameloblastoma of the mandible: a long-term follow-up. J Oral Maxillofac Surg. 1997;55(4):345-8. we can consider that the lack of recurrence in our series was a valid result.

REFERENCES

  • 1
    Sá AC, Zardo M, Paes Júnior AJ, Souza RP, Neme MP, Sabedotti I, et al. Ameloblastoma da mandíbula: relato de dois casos. Radiol Bras. 2009;37(6):465-8.
  • 2
    Avelar RL, Antunes AA, Santos TS, Andrade ESS, Dourado E. Tumores odontogênicos: estudo clínico-patológico de 238 casos. Rev Bras Otorrinolaringol. 2008;74(5):668-73.
  • 3
    Chagas JF, Toledo Júnior JI, Pascoal MBN, Pascoal MI, Aquino JL, Campos JLG, et al. Ameloblastomas: aspectos clínicos e terapêuticos. Rev Bras Cir Cabeça Pescoç o. 2007;36(3):159-62.
  • 4
    Ciment LM, Ciment AJ. Malignant ameloblastoma metastatic to the lungs 29 years after primary resection. Chest. 2002;121(4):1359-61.
  • 5
    Kim SG, Jang HS. Ameloblastoma: a clinical, radiographic, and histopathologic analysis of 71 cases. Oral Surg Oral Med Oral Pathol. 2001;91(6):649-53.
  • 6
    Swan JS. The teeth, jaws, and salivary glands. In: Juhl JH, Crummy AB, Kuhlman JE, editors. Paul & Juhl's essentials of radiologic imaging [versão digital]. 7th ed. Philadelphia: Lippincott Williams & Wilkins; 1998. p. 13-31.
  • 7
    Ogunsalu C, Daisley H, Henry K, Bedayse S, White K, Jagdeo B, et al. A new radiological classification for ameloblastoma based on analysis of 19 cases. West Indian Med J. 2006;55(6):36-41.
  • 8
    Martinez CR, Barros RM, Orué NR, Oliveira JGP, Monteiro JCC. Ameloblastoma: estudo clínico-histopatológico. Rev Cir Traumatol Buco-Maxilo-Fac. 2008;8(2):55-60.
  • 9
    Martins MD, Rosa Junior OA, Martins MAT, Bussadori SK, Fernandes KPS. Ameloblastoma: revisão de literatura. ConScientia e Saúde. 2007;6(2):269-78. Disponível em: http://www4.uninove.br/ojs/index.php/saude/article/viewFile/ 1108/886
    » Disponível em: http://www4.uninove.br/ojs/index.php/saude/article/viewFile/ 1108/886
  • 10
    Gardner DG, Pecak AM. The treatment of ameloblastoma based on pathologic and anatomic principles. Câncer. 1980;46(11):2514-9.
  • 11
    Martins RH, Andrade J, Sobrinho, Rapoport A, Rosa MP. Histopathologic features and management of ameloblastoma: study of 20 cases. São Paulo Med J. 1999;117(4):171-4.
  • 12
    Costa DO, Ecard MB, Oliveira SP, Silva LE, Dias EP, Lourenço SQC. Estudo retrospectivo dos casos diagnosticados como ameloblastoma no Serviço de Anatomia Patológica do Hospital Universitário Antônio Pedro entre 1997 e 2007. J Bras Patol Med Lab. 2008;44(6):441-7.
  • 13
    Lagares DT, Cossío PI, Guisado JMH, Pérez JL. Mandibular ameloblastoma. A review of the literature and presentation of six cases. Med Oral Patol Oral Cir Bucal. 2004;10(3):231-8.
  • 14
    Medeiros M, Porto GG, Laureano Filho JR, Portela L, Vasconcellos RH. Ameloblastoma em mandíbula. Rev Bras Otorrinolaringol. 2008;74(3):478.
  • 15
    Saddy MS, Chilvarquer I, Dib LL, Sandoval RL. Aspectos clínicos, radiográficos e terapêuticos do ameloblastoma. Rev Pós Grad. 2005;12(4):460-5. Disponível em: http://www.fo.usp.br/revistas/rpg/EDICOES/RPG-4 09 684.pdf
    » Disponível em: http://www.fo.usp.br/revistas/rpg/EDICOES/RPG-4 09 684.pdf
  • 16
    Neville BW, Damm DD, Allen CM, Bouquot JE. Patologia oral & maxilofacial. 2nd ed. Rio de Janeiro: Guanabara; 2004.
  • 17
    Nakamura N, Higuchi Y, Mitsuyasu T, Sandra F, Ohishi M. Comparison of long-term results between different approaches to ameloblastoma. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2002;93(1):13-20.
  • 18
    Olaitan AA, Arole G, Adekeye EO. Recurrent ameloblastoma of the jaws: a follow-up study. Int J Oral Maxillofac Surg. 1998;27(6):456-60.
  • 19
    Olaitan AA, Adekeye EO. Unicystic ameloblastoma of the mandible: a long-term follow-up. J Oral Maxillofac Surg. 1997;55(4):345-8.
  • Please cite this article as: de Moraes FB, Cardoso RMN, Rodrigues SV, Dutra MVF, Pereira UR, Borges TRSA. Ameloblastoma: uma análise clínica e terapêutica de seis casos. Rev Bras Ortop. 2014;49:305-308.
  • ☆☆
    Work performed in the Department of Orthopedics and Traumatology, Hospital das Clínicas, Universidade Federal de Goiás, Goiânia, GO, Brazil.

Publication Dates

  • Publication in this collection
    May-June 2014
Sociedade Brasileira de Ortopedia e Traumatologia Al. Lorena, 427 14º andar, 01424-000 São Paulo - SP - Brasil, Tel.: 55 11 2137-5400 - São Paulo - SP - Brazil
E-mail: rbo@sbot.org.br