Home Print this page Email this page Small font sizeDefault font sizeIncrease font size
Users Online: 125

 

Home About us Editorial board Search Ahead of print Current issue Archives Submit article Instructions Subscribe Advertise Contacts Login 
     

ORIGINAL ARTICLE
Year : 2009  |  Volume : 50  |  Issue : 2  |  Page : 47-51 Table of Contents     

Maxillary ameloblastoma: An enigma for the surgeon


1 Maxillofacial Unit, Ahmadu Bello University Teaching Hospital Kaduna, Kaduna State, Nigeria
2 44 Nigerian Army Reference Hospital, Kaduna, Kaduna State, Nigeria
3 Radiology Department, Ahmadu Bello University Teaching Hospital, Kaduna, Kaduna State, Nigeria
4 Pathology Department, Ahmadu Bello University Teaching Hospital, Zaria, Kaduna, Kaduna State, Nigeria

Date of Web Publication16-Nov-2010

Correspondence Address:
S O Ajike
Reader/Maxillofacial Surgeon, Ahmadu Bello University Teaching Hospital, Zaria, Kaduna
Nigeria
Login to access the Email id

Source of Support: None, Conflict of Interest: None


Rights and Permissions
   Abstract 

Background:Ameloblastoma is a benign but locally aggressive odontogenic tumour. Worldwide, maxillary ameloblastoma is rare but its late detection renders adequate treatment difficult. Majority occur in the mandible with about 5-20% occurring in the maxillary bone.
Objective: The purpose of this study was to analyze 21 cases of maxillary ameloblastoma seen and managed at the Oral and Maxillofacial Unit of Ahmadu Bello University Teaching Hospital, Zaria, Nigeria and Alba Clinic and Medical Centre, Kaduna, Nigeria.
Study Design:A retrospective study of cases of maxillary ameloblastoma from all cases of ameloblastoma seen from January 1993 to August 2008. Data with respect to patient's sex, age, tumour location, clinical presentation, radiologic features, biological and histopathologic type, surgical treatment and recurrences were analyzed.
Results:Out of 350 cases of ameloblastoma seen within the period, 21(6%) Patients were with maxillary am eloblastoma. Of the 21 cases, there were 13 males and 8 females, a male female ratio of 1.6 to 1, with an age range of 17-55 years (mean = 38.14), peaking at the 4 th and 5 th decades of life (61.9%). Tumour duration was from 3 months to 14 years. There were 18 unilateral and 3 bilateral swellings. Clinically, maxillary ameloblastoma presented with grotesque swellings, with antral involvement in 19 cases, teeth mobility/exfoliation. Radiologically, there were 20 multilocular and 1 unilocular radiolucent lesions. The most common histopathologic type was follicular (11, 52.4%).there were 22 procedures done on 21 patients; 21 maxillectomies and 1 enucleation. Follow up period of 18 patients was between 3 months and 10 years from which 3(16.7%) recurrences were observed.
Conclusion:Ameloblastum a is uncommon in the maxilla. While maxillary ameloblastoma is indistinguishable histologically from its mandibular counterpart, it is very lethal. An excellent result achieved in this study was due to the radical mode of treatment of the multilocular variety. Rehabilitation postoperatively remains a challenge. Periodic life-long follow-up is recommended.

Keywords: Iron deficiency, anaemia, pregnancy, booking, Gombe


How to cite this article:
Ajike S O, Omisakin O O, Adebayo E, Chom N D, Samaila M. Maxillary ameloblastoma: An enigma for the surgeon. Niger Med J 2009;50:47-51

How to cite this URL:
Ajike S O, Omisakin O O, Adebayo E, Chom N D, Samaila M. Maxillary ameloblastoma: An enigma for the surgeon. Niger Med J [serial online] 2009 [cited 2017 Jun 28];50:47-51. Available from: http://www.nigeriamedj.com/text.asp?2009/50/2/47/71943


   Introduction Top


Ameloblastoma is an invasive, potentially malignant neoplasm that consists of proliferating odontogenic epithelium supported by fibrous stroma [1] . It occurs in the mandible in a ratio of 5 to1 [2] . About 5 to 20% occur in the maxillary bone with majority in the molar region [3],[4] . While ameloblastom a occur in all age groups [4],[5] the maxillary ameloblastoma occur 12 years later than that of its mandibular counterpart [2] . There is no sex predilection [2] , although some authours have recorded more males than females [6],[7] while some have documented more females than males [8] .

Anatomically, the maxilla is associated with the presence of the paranasal sinuses, orbital and cranial cavities. Also, it's more cancellous nature make maxillary ameloblastoma to be more aggressive than their mandibular counterparts. Owing to the locally aggressive and infiltrative nature, a radical approach is usually advocated [7],[8],[9],[10] to reduce the recurrence rate which could be as high as 100% [8] . A long time follow-up has been advocated because recurrence 30 yeas post-operatively have been reported [11] . Because of its uniqueness an analysis of 21 cases of maxillary ameloblastoma seen and managed at the Oral and Maxillofacial Unit of Ahmadu Bello University Teaching Hospital, Zaria, Nigeria and Alba Clinic and Medical centre, Kaduna, Nigeria is presented.


   Materials and Method Top


The materials for this study consisted of a retrospective study of maxillary ameloblastoma seen and managed at the Maxillofacial Unit, Ahmadu Bello University Teaching Hospital, Kaduna and Zaria, Kaduna State, Nigeria and Alba Clinic and Medical Centre, Kaduna, Kaduna State, Nigeria. From the entire cases of 350 ameloblastoma seen between January 1993 and August 2008, medical records of patients with maxillary ameloblastoma were retrieved for analysis of patient's sex, age, tumour location, clinical presentation, radiologic features, biological and histopathologic types, surgical treatment and recurrences. Data collected was analyzed using Microsoft Excel.


   Results Top


There were 21 cases of maxillary ameloblastoma representing 6 % of total ameloblastoma seen in both hospitals during the study period under review. They were 13 males and 8 females, a. male -female ratio of 1.6 to 1 [Table 1]. The age range was between 17 and 55 years old with a mean of 38.14, majority 13 (61.9%) were in the 4 th and 5 th decades of life [Table 1]. Duration of lesion ranged between three months and 14 years. There were 18 (85.7%) unilateral and 3(14.3%) bilateral cases of maxillaay am eloblastoma [Figure 1]. While 20 (95.2%) were posterior tumours and one (4.8%)anterior tumour. Three of the posterior tumours had crossed the midline [Figure 1].
Figure 1: Bilateral maxillary ameloblastoma in a 55 year old male Nigerian.


Click here to view
Table 1: Showing age and sex distribution of 21 patients with maxillary ameloblastoma.

Click here to view


The clinical presentations varied greatly, all the 21 cases had grotesque swellings [Figure 2]. In terms of site majority, 19(90.5%) had antral involvement with two (9.5%) extending into the zygomatic bone, the temporal region and into the orbit with blindness respectively. There were involvement of nasal cavity in five (23.8%) and one (4.8%) case in the palate. Presenting complaints were teeth mobility in 12 (57.1%) cases, exfoliated teeth in 7(33.3%), nasal swelling/obstruction in 5(23.8%), ulceration of lesion in 9 (42.9%), proptosis in 3(14.3%), occlusal furrow in 10(47.6%), bleeding in 4(19.0%) and epiphora in 1(4.8%) case. Biologically, there were 18(85.7%) solid, 1(4.8%) cystic and 2 (9.5%) solid-cystic [Table 2] lesions. The histopathologic types were 11(52.4%) follicular, 3(14.3%) plexiform, 3(14.3%) follicular with squamous metaplasia and 4(19.0 %) acanthomatous [Table 2]. Radiography showed multilocular radiolucency and opacification of the maxillary sinus in 20 (95.2%) and one (4.8%) unilocular radiolucency [Figure 3]. Radical treatment was the modality of treatment in 20(95.2%) and one (4.8%) had enucleation [Table 3]. There were two (18.2%) recurrences of 11 followed up cases and (9.5%) of total cases.
Figure 2: Unilateral maxillary ameloblastoma with temporal, zygomatic bone and arch with facial nerve involvement.

Click here to view
Figure 3: Multilocular radiolucency of the left maxilla with opacification of the left maxillary antrum

Click here to view
Table 2: showing the histologic types and the gross appearance.

Click here to view
Table 3: Treatment modalities of 21 patients

Click here to view



   Discussion Top


Globally, maxillary ameloblastoma is more rare than mandibular lesions with reports in the literature often limited to case reports or case series [3],[12],[13],[14],[15],[16],[17],[18] . From our centre, the last report on ameloblastoma was by Olaitan et a1 [6] who recorded 4.7% as maxillary ameloblastoma. This current report of 21 cases of maxillary ameloblastoma collected over 15 years 8 months representing 6% of total ameloblastoma seen is in close agreement with the global ratio 1 to 5 [3],[4],[6] and reports by Tsaknis and Nelson [7] and Zwahlen and Gratz [19] of 21 and 26 cases of maxillary ameloblastoma respectively. Our study shows a male preponderance of 1.6:1 which is similar to other reports [7] but contrasts with the Zurich study by Zwahlen and Gratz [19] who have documented a female: male ratio of 1.5 to 1 and Scaccia and others [17] report of equal sex distribution.

Ameloblastoma occur at all ages [5],[7],[10],[20] however majority present during the 3 rd or 4 th decades of life. However, in the maxilla, lesions are seen more in patients over a decade older?. In this study, 61.9% were in the 4 th and 5 th decades. A mean of 38.14 recorded in our study is lower than 45.6 years recorded by Tsaknis and Nelson. [7] All our patients presented with gross maxillary swellings [Figure 1]. Maxillary ameloblastoma maybe a symptomatic. With time and growth of the tumour within the richly vascularized cancellous bone of the maxilla, tumour spreads to the adjacent paranasal sinuses, nasal cavity, nasopharynx, orbital adnexials, lacrimal apparatus, skull base and intracranial structures [7],[12],[14],[15],[19] . This results in difficulty in mastication, deglutition, loosening of teeth, epistaxis, nasal obstruction, with rhinorrhoea [12],[18],[21] . Ulceration may occur following trauma, long history or topical application of herbal medication [4],[7],[10] . While ulceration was the most common presentation in the report of Tsaknis and Nelson, in our study there were only nine cases of ulcerated lesions with a history of topical application of herbal medication in six cases.

Majority are located in the posteriorregion [5],[7] . In our series, there were 20 (95.2%) posterior tumours and only one (4.8%) anterior tumour. Posterior maxillary tumours tend to be larger and more destructive with frequent involvement of the maxillary antrum (90.5%), the zygomatic bone (9.5%), the globe (9.5%) and the temple (9.5%) as shown in [Figure 2]. One of the temporal lesions was found to have eroded the bone with facial nerve deficit [Figure 2]. Tumour site distribution in this report compares favourably with that by Tsaknis and Nelson's [7] who found one anterior lesion with the others involving the orbit, nasal floor and the maxillary sinus among 21 cases of maxillary ameloblastoma. According to Small and Waldron [4] , 21 (47%) occur in the molar region, 15(33 %) in the antrum and nasal floor; 4(9%) in the premolar and canine region respectively and 1(2 %) in the palate.

Bray et al[12] reported a maxillary ameloblastoma presenting as a nasal polyp. In this series there were five cases with nasal obstruction and one with epiphora following compression and or invasion of the nasolacrimal duct. Ophthalmic complication recorded in two cases were probably due to exposure keratitis following proptosis, involvement of the ophthalmic artery at the postern-supero-medial aspect of the maxillary sinus or by direct invasion of the globe via the intra-ocular muscles. Orbital, fronto-ethmoidal sinus, skull base and intracranial extension have resulted in the death of the patients [9],[13],[14],[15],[17] either from before or after treatment from recurrent lesions. Muller and Slootweg [9] concluded that ameloblastoma invades the spongy bones readily with little tendency of the cortical bone, with the periosteum acting as a great barrier and no definite capsule where the tumour adjoins the oral mucosa.

Extension of the tumour to the paranasal spaces makes standard radiologic diagnosis difficult [22] . Lesions usually appear as either u nil ocular or multilocular (soap bubble or honey comb) with well defined scalloped margins. Radiographic records showed 20 multilocular radiolucency with opacity of the maxillary antrum and 1 expansileunilocular lesion [Figure 3]. Incidentally, all the multilocular lesions were in the posterior region. According to Williams [23] multilocular ameloblastornas have a poorer prognosis than their unilocular counterpart. Unilocular lesions may simulate odontogenic cysts while the multilocular lesions simulate odontogenic keratocysts, fibromyxoma, giant cell granurloma and aneurysmal bone cysts. Unilocular lesions occur in younger patients [2],[24] . Coincidentally, in our series the unilocular lesion was in the youngest patient. MRI and contrast enhanced CT [25] offer the best imaging methods for visualization of extensive lesions; however in this study none was done because apart from the prohibitive cost, these hi-tech machines only became available in our centre in 2005.

Regarding the biologic gross appearance, ameloblastoma may be cystic, solid or cystic-solid, however nearly all ameloblastomas demonstrate cystic degeneration [4],[8],[26] as single tumour may occasionally exhibit the three structural characteristics [4] . Small and Waldron [4] believe that cystic degeneration is a function of age. In this study, majority 18(85.7%) were solid, 1 (4.8%) cystic and 2 (9.5%) solid-cystic. Histopathologically, follicular and plexiform patterns are the most predominant [2].[4],[8],[12] . This is similar to our study that has reported more follicular type [Table 2]. Sehdev et al. [8] believe the histopathologic types has no clinical and prognostic implications as different sections from same tumour may give mixed histologic patterns. A view contested by some authors [2],[5],[9] . Surgical approach is the accepted treatment of choice, however, there is still no consensus regarding conservative versus radical surgery. The maxillary ameloblastom a are more difficult to treat because of the combination of the well vascularized, fragile, cancellous maxillary bones, presence of the paranasal sinuses, nasal and orbital cavities which readily facilitates tumour spread to the zygomatic bone, cranial base and paracranial structures and the pterygomaxillary fissure. Radical surgery as defined by Muller and Slootweg [9] is a procedure in which ameloblastoma is removed with a marginal of normal bone by using segmental or marginal resection. However, most investigators have recommended at least between 1 cm and 3cm of surrounding healthy bone [9],[27]

[Table 3] shows the various surgical approaches used in the treatment of 21 cases of maxillary ameloblastoma. The two cases with orbital involvement had orbital exenteration of the involved globes while lesions involving the temporal region were excised. In one of the temporal lesions where there was erosion of the bone, lesion was teased off the dura mater. Enucleation is adequate for unilocular/unicystic lesions particularly for anterior lesions and where periodic follow-up is available. The most important factor in the treatment of maxillary ameloblastoma is the prevention of local recurrence which varies from 20 to 100% [6,[7],[8] . Sehdev et al[8] reported 100% recurrence rate following conservative surgery in 11 patients and 22% following radical surgery. In this study, only two (18.2%) of the 11 patients with available follow-up records had recurrence compared to 8(50%) of the 16 cases followed-up by Tsaknis and Nelson [7] . Recurrence rate of maxillary ameloblastoma is usually related to the mode of surgery, extent of the tumour presentation. The low recurrence rate in this study is due to the adoption of radical surgical procedures, which allowed for complete extirpation of tumour with sufficient safety margins in all the four dimensions. Radical surgery in our center involved the removal of tumour with a margin of between 2.5 and 3cm of apparent normal bone because majority of the patients usually default follow-up protocol in our enviornment.

Rehabilitation of maxillary defects can be achieved by the use of prosthetic obturators [29] , pedicled and free tissue transfers with or without bone grafts [28],[29],[30],[31] . In this study, 18(85.7%) of our patients had prosthetic obturator rehabilitation with good functional and aesthetic results while the remaining three (14.4%) patients (two patients with bilateral maxillectomy and the patient with total maxillectomy and right subtotal maxillectomies) were not rehabilitated resulting in both functional and psychosocial disability [Figure 4]. Rehabilitation of bilateral maxillectomized patients usually requires the use of implants.
Figure 4: Facial disfigurement following bilateral ameloblastoma

Click here to view



   Conclusion Top


Maxillary ameloblastoma is uncommon. The richly vascularized and cancellous maxillary bone facilitating extension into the paranasal sinuses, orbital and cranial cavities make maxillary ameloblastoma very lethal. Radical surgery offers best result. Rehabilitation postoperatively remains a challenge particularly in bilateral maxillectomized patients. A lifelong tune follow-up is advocated. Competing interest We hereby declare that there is no competing interest of any type.


   Acknowledgement Top


Part of this paper was presented at the 2 nd Scientific Conference of the Nigerian Association of Oral and Maxillofacial Surgeons, Obafemi Awolowo University, Ile-Ife, Oyo State, Nigeria, June 12-16,2007.

 
   References Top

1.International Histological Classification of Tumours. Histologic Typing of Odontogenic Tumours, Jaw Cysts and Allied Lesions. Monograph no. 5. Geneva: world Health Organization, 19971.  Back to cited text no. 1
    
2.Reichart P. A., Philipsen H. P., Sonner S. Ameloblastoma: biologic profile of 3677 cases. Eur J Cancer Oral Oncol 1995; 31B(2): 86-99.  Back to cited text no. 2
    
3.Small I. A., Waldron C. A. Ameloblastoma of the jaws. Oral Surg Oral Med Oral Path 1955; 8: 281-297.  Back to cited text no. 3
    
4.Iordanidis S., Makos C. H., Dirnitrakopoulos J., Kariki H. Ameloblastoma of the maxilla. Case report. Australian Dent J 1999-,44(l): 51-55.  Back to cited text no. 4
    
5.Li T. J., Wu Y. T., Yu S. F., Yu G. Y. Unicystic ameloblastoma: a clinicopathologic study of 33 Chinese patients. Am J Surg Path 2000; 24(10): 1385-1389.  Back to cited text no. 5
    
6.Tsaknis P J., Nelson J. F. The maxillary ameloblkastoma: an analysis of 24 cases. Joral Surg 1980; 38: 336-342.  Back to cited text no. 6
    
7.Olaitan A. A., Adeola D. S., Adekeye E. O. Ameloblastoma clinical features and management of 315 cases from Kaduna, Nigeria. J Crano-maxillofac Surg 1993; 21: 351-355.  Back to cited text no. 7
    
8.Sehdev M. K., Huvous A. G, Strong E. W, Gerold E. P., Willis G W Ameloblastoma of the maxilla and mandible. Cancer 1974; 33:324-333.  Back to cited text no. 8
    
9.Adekeye E. O. Ameloblastoma of the jaws: a survey of 109 patients. J Oral Surg 1980; 38: 36-41.  Back to cited text no. 9
    
10.Muller H., Slootweg P. J. The ameloblastoma: controversial approach to therapy. J maxillofac Surg 1985-,13: 79.  Back to cited text no. 10
    
11.Hayward J. R. Recurrent ameloblastoma 30 years after surgical treatment. J Oral Surg 1973; 31: 368-370.  Back to cited text no. 11
    
12.Bray D., Michael A., Falconer D. T., Kaddouur H. S. Ameloblastoma: a rare nasal polyp. J Laryngol Otol 2007,121: 72-75.  Back to cited text no. 12
    
13.Wenig B. L., Sciubba J. J., Cohen A., Goldstein A., Abramson A. L. An unsual cause of nasal obstruction: ameloblastoma. Otolaryngol Head Neck Surg 1985; 95: 426-432.  Back to cited text no. 13
    
14.Scaccia F. J., Strauss M., Arnold J., Maniglia A. J. Maxillary arneloblastoma: a case report. Am Jotolaryngol 1991;12: 2025.  Back to cited text no. 14
    
15.Bredenkamp J. K., Zimmerman M. C., Mickel R. A. Maxillary ameloblastoma: a potentially lethal neoplasm. Arch Otolaryngol Head Neck Surg 1989; 115: 99-104.  Back to cited text no. 15
    
16.Komisar A. Plexiform ameloblastoma of the maxilla with extension to the skull base. Head Neck Surg 1984; 7: 172-1 7 5.  Back to cited text no. 16
[PUBMED]    
17.Sapundziev P, Ilieva N. Maxillary ameloblastoma- report of 3 cases. Serbian Dent J 2005; 52: 229-236.  Back to cited text no. 17
    
18.Chaudhuri P. ameloblastoma of the upper jaw. J Laryngol Otol 1975; 89(4): 457-465.  Back to cited text no. 18
    
19.Zwahlen R. A., Gratz K. W. Maxillary ameloblastoma: a review of the literature and of a 15 year database. J Cranomaxillofac Surg 2002; 30(5): 273-279.  Back to cited text no. 19
    
20.Adebayo E. T., Ajike S. 0., Adekeye E. O. A review of 318 odontogenic tumours in Kaduna, Nigeria. J Oral Maxillofac Surg 2005; 63: 811-819.  Back to cited text no. 20
    
21.Shaw H. J., Katsakis D. K. Arneloblastoma of the maxilla: a clinical study with 4 cases. J Laryngol Otol 1972;873-874.  Back to cited text no. 21
    
22.Shatkin S., Hoffmeister J. F. Ameloblastoma: a rational approach to therapy. Oral Surg Oral Med Oral Path 1965; 20: 336-341.  Back to cited text no. 22
    
23.Williams T. P. Management of ameloblastoma: a changing perspective. J Oral Maxillofac Surg 1993; 51: 1064-1070.  Back to cited text no. 23
    
24.Junquera L., Ascani G, Vicenti J. C., Garcia-Consuegra L., Roig P. Ameloblastoma revisited. Ann Otol Rhino Laryngol 2003;112(12):1034-1039.  Back to cited text no. 24
    
25.Kawai T., Murakami S., Kishino M., Matsuya T., Sakada M., Fuchihata H. diagnostic imaging in two cases of recuurent maxillary ameloblastoma: comparative evaluation of plain radiographs, CT and MR images. Br J Oral Maxillofac Surg 1998; 36(4): 304-310.  Back to cited text no. 25
    
26.Robinson H. C. G. Ameloblastoma. A survey of three hundred and sixty-nine cases from the literature. Arch Path 1937; 23: 831-843.  Back to cited text no. 26
    
27.Chapell J., Stoelinger P., Wide P., Brouns J., Voorsmit R. Rational approach to diagnosis and treatment of ameloblastoma and odontogenic keratocysts. Br J Oral Maxillofac Surg 2004; 42: 381-390.  Back to cited text no. 27
    
28.Rogers S. N., Lowe D., McNally D., Brown J. S., Vaughn E. D. Health related quality of life after maxillectomy: a comparison between prosthetic obturator and free flap. J Oral Maxillofac Surg 2003: 61: 174-181.  Back to cited text no. 28
    
29.Brown J. S., Jones D. C., Summerwill A., Rogers S. N., Howell R. A., Cawood J. I., Vaughn E. D. Vascularized iliac crest with internal oblique muscle for immediate reconstruction after maxillectomy. Br J Oral Maxillofac Surg 2002; 40: 183-190.  Back to cited text no. 29
    
30.Smolka W, Iizuka T. Surgical reconstruction of maxilla and midface: clinical outcome and factors relating to postoperative complications. J Craniomaxillofac Surg 2005; 33:1-7.  Back to cited text no. 30
[PUBMED]  [FULLTEXT]  
31.Urken M. I., Bridger A. G., Zur K. B., Genden E. M. The scapular osteofasciocutaneous flap: a 12 year experience. Arch Otolaryngol Head Neck Surg 2001; 127: 862-869.  Back to cited text no. 31
    


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4]
 
 
    Tables

  [Table 1], [Table 2], [Table 3]



 

Top
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
    Abstract
    Introduction
    Materials and Method
    Results
    Discussion
    Conclusion
    Acknowledgement
    References
    Article Figures
    Article Tables

 Article Access Statistics
    Viewed5715    
    Printed181    
    Emailed0    
    PDF Downloaded358    
    Comments [Add]    

Recommend this journal