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An Official Publication of the Indian Association of Oral and Maxillofacial Pathologists


 
  Table of Contents    
CASE REPORT  
Year : 2021  |  Volume : 25  |  Issue : 1  |  Page : 159-162
 

Maxillary ameloblastic carcinoma: A diagnostic conundrum


1 Reader, Department of Oral Pathology and Microbiology, Buddha Institute of Dental Sciences and Hospital, Patna, Bihar, India, India
2 Oral Maxillofacial Pathology Clinic, West Bengal, India
3 Senior Lecturer, Mithila Minority Dental College and Hospital, Darbhanga, Bihar, India

Date of Submission18-Feb-2020
Date of Acceptance03-Nov-2020
Date of Web Publication14-May-2021

Correspondence Address:
Manisha Shrikaar
J- 182, P. C. Colony, Kankarbagh, Patna - 800 020, Bihar
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jomfp.JOMFP_71_20

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   Abstract 


Ameloblastic carcinoma (AC) is a rare malignant epithelial proliferation that is associated with an ameloblastoma or histologically resembles an ameloblastoma. It is considered to be an aggressive neoplasm that is locally invasive and spread to regional lymph nodes or distant sites. It requires aggressive surgical treatment, and regular follow-up, therefore, differs from ameloblastoma. Sometimes, ameloblastomas exhibit a mild-to-moderate degree of cytological atypia; hence, in such cases, a correlation should be established between the clinical, radiological and histopathological findings, thus detecting the aggressiveness of the tumor. Here, we present the case report of a 52-year-old male patient diagnosed as AC based on histopathological and immunohistochemical findings.


Keywords: Ameloblastic carcinoma, ameloblastoma, cytological atypia, immunohistochemistry


How to cite this article:
Shrikaar M, Suwasini S, Chatterjee K, Sinha S. Maxillary ameloblastic carcinoma: A diagnostic conundrum. J Oral Maxillofac Pathol 2021;25:159-62

How to cite this URL:
Shrikaar M, Suwasini S, Chatterjee K, Sinha S. Maxillary ameloblastic carcinoma: A diagnostic conundrum. J Oral Maxillofac Pathol [serial online] 2021 [cited 2021 Jun 12];25:159-62. Available from: https://www.jomfp.in/text.asp?2021/25/1/159/316058





   Introduction Top


Odontogenic neoplasm derives from epithelial and mesenchymal remnants of the tooth germ that are classified into benign and malignant tumors. The malignant odontogenic neoplasm is extremely challenging to study due to their rarity of occurrence. Most of what we know regarding these malignant neoplasms is derived from either few case reports or small case series. The limited number of cases makes it difficult to establish standardized diagnostic criteria and tumor clinical characterization.[1],[2],[3]

The term ameloblastic carcinoma (AC) was introduced by Elzay in the year 1982.[4] AC is one such rare odontogenic malignancy accounting for 1.5%–2.0% of all malignant odontogenic tumors. It has features of ameloblastoma intermingled with features of carcinoma, regardless of whether it has metastasized, i.e., ameloblastoma in which there is histological malignant transformation.[5],[6] The term malignant ameloblastoma is confined to those ameloblastomas that metastasize despite an apparently typical benign histology in both the primary and metastatic lesions.[7] The incidence ratio of AC to malignant ameloblastoma was found to be 2:1.[8]

Most of the ACs appear to be of the primary type.[9] Only six cases of secondary AC have been reported.[10] Clinically, AC is aggressive, locally invasive and causes distant metastasis.[9] Here, in this article, we report a rare case of AC of the maxilla with clinical, radiological and histopathological features along with the Immunohistochemical (IHC) findings.


   Case Report Top


A 52-year-old male patient presented with the chief complaint of pain and swelling in the upper right anterior region for the past 8 months. The patient gave a history of trauma in the same region, after which the swelling had developed and gradually increased in size. The patient was prescribed with analgesic and antibiotic by a local physician, but there was no relief in the symptoms, and hence referred to the institute. Extraoral examination revealed a diffuse swelling of size 4.5 cm × 3.5 cm present on the right side of the face (maxilla), anteroposteriorly 1 cm behind the ala of the nose to the lobe of the ear and superoposteriorly occupying themed region of the face. The swelling had evolved over a period of 8 months. The swelling was firm in consistency and painful, and no local rise of temperature was found [Figure 1].
Figure 1: Clinical picture showing a diffuse extraoral swelling of size 4.5 cm × 3.5 cm present on the right side of the face (maxilla)

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On intraoral examination, erythematous growth was seen on the right side of the maxilla extending from 14 to 17 [Figure 2].
Figure 2: Intraoral picture showing erythematous growth on the right side of the maxilla extending from 14 to 17

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Radiographic examination revealed ill-defined radiolucency and significant bone loss on the right side of the maxilla. Destruction of the lower orbital margin can also be seen. Root resorption of 16 was seen [Figure 3].
Figure 3: Radiograph revealing ill-defined radiolucency and significant bone loss on the right side of the maxilla

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Based on the clinical examination and radiographic finding, a provisional diagnosis of ameloblastoma was considered. Differential diagnoses of odontogenic keratocyst, primary intraosseous carcinoma and metastatic neoplasm were considered.

After obtaining an informed consent, an incisional biopsy was performed to arrive at a definitive diagnosis.

Microscopic examination of hematoxylin and eosin stained histopathological revealed the presence of odontogenic epithelium in various patterns, predominantly in follicular pattern. Sheets like arrangement of the odontogenic epithelial cells were also seen with hyperchromatic nuclei and scanty cytoplasm. Few of the follicles showed stellate reticulum-like cells. There was evidence of increase in cellular atypia and mitotic activity. Connective tissue stroma was fibrocellular [Figure 4].
Figure 4: Odontogenic epithelium in follicular pattern, few of the follicles showing stellate reticulum-like cells, along with increase in cellular atypia and mitotic activity

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Based on histopathological examination, a diagnosis of AC was established. To further confirm the diagnosis, immunohistochemistry was performed. The sections were stained with CK19 and were found to be positive [Figure 5].
Figure 5: CK19 was found to be positive

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Thus, histopathology and immunohistochemistry confirmed the diagnosis of AC.


   Discussion Top


AC is a rare odontogenic malignancy that has histologic features of both ameloblastoma and carcinoma. In the World Health Organization (WHO) classification, published in 2005, AC was defined as a rare odontogenic malignancy that combines the histological features of ameloblastoma with cytological atypia even in the absence of metastases.

Malignant epithelial odontogenic tumors included in the 2017 WHO classification are primary intraosseous carcinoma, sclerosing odontogenic carcinoma, clear cell odontogenic carcinoma and ghost cell odontogenic carcinoma.[11] AC has been classified into two types: primary and secondary. The former develops de novo, and the latter develops by malignant transformation of a preexisting benign ameloblastoma.[12],[13]

The mean age of occurrence has been found to be 53.5 years, but the age range for AC has been found to be 51–84 years.[14] A male predominance has been reported, and similar to ameloblastoma, the mandibular posterior region is the common site associated with AC.[15] In this case report, the patient presented with swelling in the maxillary posterior region. Uzawa et al. presented a case report of maxillary AC.[12]

AC is the malignant counterpart of ameloblastoma, and BRAF V600E mutation has been found which is identical to those in other ameloblastic neoplasms.[11]

The clinical symptoms of AC are similar to ameloblastoma except few other features seen in AC are the aggressive and painful growth is more aggressive, painful, trismus, dysphonia and perforation of cortical plates is observed in AC.[11]

The radiographic appearance is usually similar to that of ameloblastoma except for the presence of focal radio-opacities which reflects dystrophic calcifications. The case described in this report also showed similar radiological features with destruction of the cortical plate. In this case, we found complete destruction of the cortical plates but no radio-opacities. Corio et al. reported that dystrophic calcification is not specific to ACs but can be seen in the desmoplastic variant of ameloblastoma.[15]

Histopathologically, AC is similar to ameloblastoma except for it will exhibit cytological atypia is seen in both primary and metastatic ACs. However, the classical features of ameloblastoma including reverse polarity and peripheral palisading are lost. So pleomorphism, altered nuclear–cytoplasmic ratio, abnormal mitoses and vascular or nerve invasion are considered to be important features for the diagnosis. The presence of necrosis may be helpful. The mitotic rate is usually increased, but the increase in mitotic activity alone is not valuable.[16],[17]

Few of the histopathological differential diagnoses included were primary intraosseous carcinoma, basaloid squamous cell carcinoma, mucoepidermoid carcinoma and acanthomatous ameloblastoma.

The various IHC markers for AC are CK19, Ki-67, MMP-2 and MMP-9. In this case, we conducted IHC with CK19 on the sections and found it to be positive.

There are four points in the clinical criteria that can be helpful for the diagnosis of AC such as rapid growth, tendency to perforate the cortex, pain and paresthesia that are distinct from their benign counterpart.[17]

The treatment for AC is radical surgical resection along with chemotherapy and radiotherapy as an adjunct.


   Conclusion Top


Ameloblastic carcinoma is a rare malignant odontogenic tumor exhibiting histologic atypical changes and hence should be differentiated from its benign counterpart ameloblastoma. Ameloblastic carcinoma should be included in the differential diagnosis of those cases where the patient is presenting with rapid growth, pain and perforation of the cortex.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
   References Top

1.
Woolgar JA, Triantafyllou A, Ferlito A, Devaney KO, Lewis JS Jr., Rinaldo A, et al. Intraosseous carcinoma of the jaws: A clinicopathological review. Part II: Odontogenic carcinomas. Head Neck 2013;35:902-5.  Back to cited text no. 1
    
2.
Eversole LR. Malignant epithelial odontogenic tumors. Semin Diagn Pathol 1999;16:317-24.  Back to cited text no. 2
    
3.
Panda S, Sahoo SR, Srivastav G, Padhiary S, Dhull KS, Aggarwal S. Pathogenesis and nomenclature of odontogenic carcinomas: revisited. J Oncol 2014;2014:197425.  Back to cited text no. 3
    
4.
Elzay RP. Primary intraosseous carcinoma of the jaws. Review and update of odontogenic carcinomas. Oral Surg Oral Med Oral Pathol 1982;54:299-303.  Back to cited text no. 4
    
5.
Shnawa IM. Otolyngologic mucosal immune compartment. Otolaryngol Open Access J 2017;2:147.  Back to cited text no. 5
    
6.
Shnawa IM. Neck surgery versus neck immunology. J Head Neck Spin Surg 2017;1:102.  Back to cited text no. 6
    
7.
Slootweg PJ, Müller H. Malignant ameloblastoma or ameloblastic carcinoma. Oral Surg Oral Med Oral Pathol 1984;57:168-76.  Back to cited text no. 7
    
8.
Regezi JA, Kerr DA, Courtney RM. Odontogenic tumors: Analysis of 706 cases. J Oral Surg 1978;36:771-8.  Back to cited text no. 8
    
9.
Neville BW, Damm DD, Allen CM, Chi AC. Oral and Maxillofacial Pathology. 4th ed.. Philadelphia: WB Saunder; 2016.  Back to cited text no. 9
    
10.
Cizmecý O, Aslan A, Onel D, Demiryont M. Ameloblastic carcinoma ex ameloblastoma of the mandible: Case report. Otolaryngol Head Neck Surg 2004;130:633-4.  Back to cited text no. 10
    
11.
Wright JM, Soluk Tekkesin M. Odontogenic tumors: Where are we in 2017? J Istanb Univ Fac Dent 2017;51:S10-30.  Back to cited text no. 11
    
12.
Uzawa N, Suzuki M, Miura C, Tomomatsu N, Izumo T, Harada K. Primary ameloblastic carcinoma of the maxilla: A case report and literature review. Oncol Lett 2015;9:459-67.  Back to cited text no. 12
    
13.
Thompson L. World Health Organization classification of tumours: Pathology and genetics of head and neck tumours. Ear Nose Throat J 2006;85:74.  Back to cited text no. 13
    
14.
Dhir K, Sciubba J, Tufano RP. Ameloblastic carcinoma of the maxilla. Oral Oncol 2003;39:736-41.  Back to cited text no. 14
    
15.
Corio RL, Goldblatt LI, Edwards PA, Hartman KS. Ameloblastic carcinoma: A clinicopathologic study and assessment of eight cases. Oral Surg Oral Med Oral Pathol 1987;64:570-6.  Back to cited text no. 15
    
16.
Hall JM, Weathers DR, Unni KK. Ameloblastic carcinoma: An analysis of 14 cases. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2007;103:799-807.  Back to cited text no. 16
    
17.
Kruse AL, Zwahlen RA, Grätz KW. New classification of maxillary ameloblastic carcinoma based on an evidence-based literature review over the last 60 years. Head Neck Oncol 2009;1:31.  Back to cited text no. 17
    


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]



 

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    Abstract
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