Jordi | Journal of Oral Diagnosis Online Submission Review an Article SOBEP - Sociedade Brasileira de Estomatologia e Patologia Oral
Volume 3 - 2018

Case Report

DOI: 10.5935/2525-5711.20180002

Aggressive adenomatoid odontogenic tumor: an uncommon case report and discussion on the differential diagnosis

John Lennon Silva Cunha1; Juliana Batista Melo da Fonte2; Maria de Fátima Batista de-Melo2; Rose Nely Pereira Filho1; Ricardo Luiz Cavalcanti de Albuquerque Júnior1

1. Tiradentes University, Department of Dentistry - Aracaju - Sergipe - Brasil
2. Federal University of Sergipe, Department of Dentistry - Aracaju - Sergipe - Brasil

Corresponding authors: John Lennon Silva Cunha

Article received on January 18, 2018.
Article accepted on February 21, 2018.



Differential diagnosis between ameloblastomas (AMB) and adenomatoid odontogenic tumor (AOT) seldom cause difficulties due to classic histopathological presentations. Adenoid ameloblastoma with dentinoid (AAD) is a rare variant of AMB which can be misdiagnosed as AOT. We report a case of a 12-year-old female presenting a painless swelling in the anterior region of the mandible. Panoramic radiograph and cone beam CT scans demonstrated large unilocular osteolytic lesion extending from 44 to 32 and involving the impacted 43. Tumor caused teeth displacement and both vestibular and lingual cortical perforation. Histopathology revealed cuboidal and spindle-shaped cells arranged in nests and rosettes, solid, duct-like and whorled areas, and foci of calcification and dentin-like material were evident. The diagnosis was aggressive AOT. Because of the similarities of the histologic features of AOT and AAD, we intend to provide a discussion on the clinicopathologic criteria for establishing the differential diagnosis of these entities

Keywords: Ameloblastoma; Diagnosis, Differential; Mandible.



The adenomatoid odontogenic tumor (AOT) is a rare benign odontogenic lesion, that is slow-growing and non-invasive, although few aggressive cases have been reported1-3. In the past years, an unusual variant of ameloblastoma presenting histological characteristics that overlap those observed in AOT has been reported under the name of adenoid ameloblastoma with formation of dentinoid (AAD)4, which may cause difficulties in the differential diagnosis. Thus, the purpose of this work is to report a case of aggressive AOT and discuss the criteria for differential diagnosis of this lesion, especially with AAD.


A 15-year-old white female patient sought the service of the stomatology clinic at Tiradentes University (Aracaju/SE) complaining of swelling in the mandible. The intraoral examination revealed a painless volume increase in the anterior region of the mandible, extending from tooth 44 to 32, firm to palpation, covered by normal-colored mucosa and with the evolution time of 5 months.

No previous history of trauma was reported by the patient. Previous medical history was not contributory. Imaging exams revealed unilocular osteolytic lesion extending from tooth 44 to tooth 32 and involving the impacted 43, causing cortical bulging and perforation (Figures 1, 2 and 3). The provisional diagnosis of AOT was established and an incisional biopsy of the lesion was performed.

Figure 1. Panoramic radiograph showing unilocular radiolucent lesion with regular margins and well-defined borders, associated with the non-erupted tooth 43 and causing dental displacement of teeth 41, 42 and 44.

Figure 2. Cone-beam computed tomography (axial cuts) showing hypodense lesion with discrete hyperdense foci within and surrounding the tooth 43. Note discontinuity of the buccal cortex.

Figure 3. Cone-beam computed tomography (sagittal cuts) showing hypodense lesion with hyperdense foci involving the tooth 43. The tumor caused both vestibular and lingual cortical perforation.

The surgical specimen was submitted to the Service of Oral Pathology of the School of Dentistry at Tiradentes University. Histopathological examination of the incisional biopsy revealed cubic and fusiform cells arranged as nests and rosettes, pseudoductal structures and solid vortex areas. Foci of dystrophic calcification and deposition of dentinoid material were evident (Figure 4). The diagnosis was agressive AOT. The patient was submitted to surgical enucleation of the lesion and is under proservation without signs of recurrence 2 years after surgery.

Figure 4. Histological sections stained with hematoxylin-eosin. (A) Compact proliferation of odontogenic epithelial cells forming nodules of cuboid and ovoid cells surrounded by fusiform cells arranged in a vortex pattern, and forming multiple pseudoductal structures (100x). (B) Solid sheets and (C) strands of epithelial cells intercalated with deposition of eosinophilic material resembling dentinoid (arrows) (400 x). (D) Formation of typical nodular, pseudoductal structures and epithelial rosettes (400x).


The latest WHO classification of odontogenic tumors defines AOT as being a proliferation of odontogenic epithelium exhibiting a variety of histoarchitectural patterns embedded in mature connective tissue stroma characterized by slow and noninvasive growth5. Compared to ameloblastomas, AOT is a non-aggressive tumor, which exhibits limited growth and accounts for about 1% to 9% of all odontogenic tumors. However, few reports of aggressive AOTs1-3, such as ours, have been reported in the literature.

The epidemiological profile shows predilection for female and young patients, with a peak prevalence in the second decade of life. Clinically, AOT usually manifests as an asymptomatic increase in volume in the anterior region of the gnathic bones, most commonly in the region of upper lateral incisors and upper canines6. Thus, this report is in consonance with the demographic characteristics classically described for AOT. However, the anatomical site involved and the pattern of tumor growth, causing bulging and cortical rupture are uncommon for this lesion and little reported in the literature. Some authors suggest that this possible aggressive behavior is due to the relatively higher growth rate in young patients, and the delay to seek professional assistance3,7.

The AOT has three clinicopathological variants: follicular, extrafollicular and peripheral. The follicular variant is associated with an unruptured tooth, as in the present case, and accounts for about 73% of the cases. The extrafollicular variant is also a central lesion, however, it is not associated with an unruptured tooth and accounts for 24% of all AOTs. Extraosseous or peripheral lesions are very rare (about 3% of cases) and clinically appear as sessile nodules in the maxillary gingiva, mimetizing common reactive fibrous lesions of the gingiva3. It is important to emphasize that all variants of the AOT share the same histopathological characteristics.

Radiographically, the follicular pattern is characterized as a well delimited radiolucent area, frequently exhibiting discrete radiopaque foci inside and associated with an unruptured tooth, usually the upper canine. The extrafollicular pattern has no association with dental elements and, normally, the radiolucent image is located between two roots, resembling a lateral periodontal cyst8. Peripheral AOTs rarely exhibit radiographic imaging; however, slight erosion of the alveolar bone cortex underlying the lesion has been reported9.

Rarely, the lesion manifests itself without a radiopaque component; however, the follicular variant, when the radiopaque foci are incipient and the image is radiolucent, may simulate a dentigerous cyst, although in AOT the tooth inserted in the lesion is not necessarily limited to the amelocemental junction as seen in the latter6,10. Radiopaque foci were not observed on the panoramic radiograph in our case, but were identified on the CT scan. Compared with conventional radiographs, computed tomography exhibits this advantage and, therefore, may guide better the diagnosis of such lesions. The presence of calcifications excludes the diagnosis of a dentigerous cyst6,10.

Due to the variety of clinical/radiographic appearances, AOT has several differential diagnoses, varying according to the presence and degree of radiopacity found in lesions and whether or not it is associated with an unruptured tooth. Radiolucent images may mimetize the appearance of dentigerous cysts, odontogenic keratocysts and ameloblastomas, as lesions exhibiting radiopaque foci can be confused with calcifying cystic odontogenic tumor and even calcifying epithelial odontogenic tumor1-3.

Histologically, AOT is characterized by the compact proliferation of epithelial cells exhibiting cuboid and/or fusiform shape, permeated by scarce connective tissue stroma. Epithelial tumor cells form sheets, nests, cords, rosette-like structures and pseudoductal structures, formed by cuboidal or columnar cells exhibiting nuclei with polarization opposite to the lumen. Dystrophic calcification foci and areas of deposits of amorphous eosinophilic material with dentinoid appearance are also noted. At the periphery, thick capsule of dense fibrous connective tissue can also be seen surrounding the tumor1-3,9. Similar characteristics were observed in the present case.

Although the differential diagnosis between ameloblastoma and AOT rarely causes difficulties, adenoid ameloblastoma with dentinoid (AAD) may be confused with aggressive forms of AOT. AAD is considered to be an unusual aggressive variant of ameloblastoma described in 1994 by Brannon as a parenchymal proliferation similar to AOT associated with areas with typical ameloblastic differentiation. In addition, the deposition of dentinoid material in the lesion was observed, causing the tumor to be defined as AAD11.

From its initial description, other reports of similar cases were published in the literature emphasizing the potential of local aggression and recurrence of these lesion4,12-18. Proliferations similar to AOT had already been found focally in ameloblastomas, however, these findings were interpreted as a possible variation of differentiation, but irrelevant to the biological behavior of the lesion19-21. Loyola et al.4 reported that the recurrence rate of AAD was approximately 75%, even when patients underwent radical surgery. A much higher rate than those often cited for conventional ameloblastomas and ameloblastic carcinomas22-24.

This high rate of recurrence can be explained in a number of ways, namely, the predilection of the AAD for the posterior maxilla, making the complete excision with adequate margin more difficult, or the inherent biological nature of the lesion, evidenced by the high proliferative index (Ki-67)4. In addition, it should be noted that in some previously published reports of recurrent AAD, patients were initially treated with simple enucleation because the lesions were misdiagnosed as AOT15,16.

Table 1 shows some of the main differences between aggressive AOT and AAD. Given these data, the case in question should, in fact, be framed as an uncommon aggressive presentation of AOT, since no typical ameloblastomatous areas were observed, an essential feature for suspected AAD to be considered. The evident clinical aggressiveness and the high recurrence rates of AAD compared to AOT, which exhibits limited growth and almost zero recurrence tendency, makes the precise distinction between these two entities a particularly important issue, which can greatly influence the treatment and prognosis of the lesion.

Conservative surgical excision is the treatment of choice for AOTs1-3,25. Due to the low recurrence reported in the literature, conservative treatment was safely proposed. The patient underwent surgical enucleation of the lesion and after 24 months of follow-up, no relapse was observed. However, careful monitoring should be done, especially in our case, considering the unusual presentation and aggressive behavior of the tumor.


1. Oliveira MR, Gabrielli MA, Gabrielli MF, De Andrade CR, Silva BN, Pereira-Filho VA. Unusual Adenomatoid Odontogenic Tumor. J Craniofac Surg. 2016;27:e139-41. DOI: 10.1097/SCS.0000000000002391

2. Narayanan VS, Naidu G, Ragavendra R, Mhaske-Jedhe S, Haldar M. Adenomatoid odontogenic tumor of the mandible with unusual radiographic features: A case report. Imaging Sci Dent. 2013;43:111-5. DOI: 10.5624/isd.2013.43.2.111

3. Dhupar V, Akkara F, Khandelwal P. An unusually large aggressive adenomatoid odontogenic tumor of maxilla involving the third molar: A clinical case report. Eur J Dent. 2016;10:277-80. DOI: 10.4103/1305-7456.178308

4. Loyola AM, Cardoso SV, de Faria PR, Servato JP, Eisenberg AL, Dias FL, et al. Adenoid ameloblastoma: clinicopathologic description of five cases and systematic review of the current knowledge. Oral Surg Oral Med Oral Pathol Oral Radiol. 2015;120:368-77. DOI: 10.1016/j.oooo.2015.05.011

5. Wright JM, Vered M. Update from the 4th Edition of the World Health Organization Classification of Head and Neck Tumours: Odontogenic and Maxillofacial Bone Tumors. Head Neck Pathol. 2017;11:68-77. DOI: 10.1007/s12105-017-0794-1

6. Philipsen HP, Reichart PA, Siar CH, Ng KH, Lau SH, Zhang X, et al. An updated clinical and epidemiological profile of the adenomatoid odontogenic tumour: a collaborative retrospective study. J Oral Pathol Med. 2007;36:383-93. DOI: 10.1111/j.1600-0714.2007.00536.x

7. Mohamed A, Singh AS, Raubenheimer EJ, Bouckaert MM. Adenomatoid odontogenic tumour: review of the literature and an analysis of 33 cases from South Africa. Int J Oral Maxillofac Surg. 2010;39:843-6. DOI: 10.1016/j.ijom.2010.06.014

8. More C, Das S, Gupta S, Bhavsar K. Mandibular adenomatoid odontogenic tumor: Radiographic and pathologic correlation. J Nat Sci Biol Med. 2013;4:457-62. DOI: 10.4103/0976-9668.116965

9. Garg D, Palaskar S, Shetty VP, Bhushan A. Adenomatoid odontogenic tumor - hamartoma or true neoplasm: a case report. J Oral Sci. 2009;51:155-9. DOI: 10.2334/josnusd.51.155

10. Manjunatha BS, Harsh A, Purohit S, Naga MV. Adenomatoid odontogenic tumor associated with a dentigerous cyst. J Cancer Res Ther. 2015;11:649. DOI: 10.4103/0973-1482.138120

11. Brannon RB. Adenoid Ameloblastoma with Dentinoid. Washington: Armed Forces Institute of Pathology. ROPCOM; 1994. p. 1-94.

12. Kumar K, Shetty DC, Wadhwan V, Dhanapal R, Singh HP. Dentinoameloblastoma with ghost cells: A rare case report with emphasis on its biological behavior. Dent Res J (Isfahan). 2013;10:103-7. DOI: 10.4103/1735-3327.111809

13. Saxena K, Jose M, Chatra L, Sequiera J. Adenoid ameloblastoma with dentinoid. J Oral Maxillofac Pathol. 2012;16:272-6. DOI: 10.4103/0973-029X.99088

14. Sonone A, Hande A, Chaudhary M, Bonde R, Sheorain A, Agni N. Adenoid ameloblastoma with dentinoid and ghost cells. A composite odontogenic tumour: a rare case report and review of the literature. Oral Surg. 2011;4:77-81. DOI: 10.1111/j.1752-248X.2010.01109.x

15. Ide F, Mishima K, Saito I, Kusama K. Diagnostically challenging epithelial odontogenic tumors: A selective review of 7 jawbone lesions. Head Neck Pathol. 2009;3:18-26. DOI: 10.1007/s12105-009-0107-4

16. Evans BL, Carr RF, Phillipe LJ. Adenoid ameloblastoma with dentinoid: A case report. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2004;98:583-8. DOI: 10.1016/S1079210404001866

17. Matsumoto Y, Mizoue K, Seto K. Atypical plexiform ameloblastoma with dentinoid: Adenoid ameloblastoma with dentinoid. J Oral Pathol Med. 2001;30:251-4. DOI: 10.1034/j.1600-0714.2001.300410.x

18. Rai HK, Pai SM, Dayakar A, Supriya H. Adenoid ameloblastoma with dentinoid: A rare hybrid variant. J Oral Maxillofac Pathol. 2017;21:319. DOI: 10.4103/jomfp.JOMFP_53_15

19. Yamazaki M, Maruyama S, Abé T, Babkair H, Fujita H, Takagi R, et al. Hybrid ameloblastoma and adenomatoid odontogenic tumor: report of a case and review of hybrid variations in the literature. Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;118:e12-8. DOI: 10.1016/j.oooo.2013.08.032

20. Ngwenya SP, Raubenheimer EJ, Noffke CE. Internal morphology of ameloblastomas: a study of 24 resected specimens. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009;108:754-62. DOI: 10.1016/j.tripleo.2009.06.026

21. Raubenheimer EJ, van Heerden WF, Noffke CE. Infrequent clinicopathological findings in 108 ameloblastomas. J Oral Pathol Med. 1995;24:227-32. DOI: 10.1111/j.1600-0714.1995.tb01172.x

22. Fregnani ER, da Cruz Perez DE, de Almeida OP, Kowalski LP, Soares FA, de Abreu Alves F. Clinicopathological study and treatment outcomes of 121 cases of ameloblastomas. Int J Oral Maxillofac Surg. 2010;39:145-9. DOI: 10.1016/j.ijom.2009.11.022.

23. Yoon HJ, Hong SP, Lee JI, Lee SS, Hong SD. Ameloblastic carcinoma: an analysis of 6 cases with review of the literature. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009;108(6):904-13. DOI: 10.1016/j.tripleo.2009.06.045

24. Reichart PA, Philipsen HP, Sonner S. Ameloblastoma: Biological profile of 3677 cases. Eur J Cancer Part B Oral Oncol. 1995;31:86-99. DOI: 10.1016/0964-1955(94)00037-5

25. Swasdison S, Dhanuthai K, Jainkittivong A, Philipsen HP. Adenomatoid odontogenic tumors: an analysis of 67 cases in a Thai population. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008;105:210-5. DOI: 10.1016/j.tripleo.2007.02.020

26. Koneru A, Hallikeri K, Nellithady GS, Krishnapillai R, Prabhu S. Immunohistochemical expression of calretinin in ameloblastoma, adenomatoid odontogenic tumor, and keratocystic odontogenic tumor: a comparative study. Appl Immunohistochem Mol Morphol. 2014;22:762-7. DOI: 10.1097/PAI.0000000000000005


© Copyright 2019 - Jordi - All rights reserved GN1