Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contacts Login 
  • Users Online: 669
  • Home
  • Print this page
  • Email this page


 
 Table of Contents  
CASE REPORT
Year : 2023  |  Volume : 20  |  Issue : 1  |  Page : 77

Keratoameloblastoma of the lower jaw: A rare challenging entity


1 Department of Oral and Maxillofacial Pathology, Tehran University of Medical Sciences, Tehran, Iran
2 HCA South Atlantic Division, Trident Medical Center, Charleston, South Carolina, USA
3 Department of Pathology, Cancer Institute Hospital, IKHC, Tehran University of Medical Sciences, Tehran, Iran

Date of Submission04-Mar-2023
Date of Acceptance14-May-2023
Date of Web Publication25-Jul-2023

Correspondence Address:
Dr. Pouyan Aminishakib
North Amirabad, School of Dentistry, 1439955991, Tehran
Iran
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/1735-3327.382130

Rights and Permissions
  Abstract 


Ameloblastoma is the second most common benign odontogenic tumor with various histopathologic features. Except for the unicystic type of ameloblastoma, the different microscopic patterns of this tumor show no significant correlation with long-term clinical behavior. During recent decades, additional challenging subtypes of ameloblastoma, including “Keratoameloblastoma” (KA), have been introduced in the literature. Here, we present a case of KA and discuss the important diagnostic microscopic features.

Keywords: Ameloblastoma, jaw neoplasms, odontogenic tumors


How to cite this article:
Moradi M, Neville BW, Aminishakib P. Keratoameloblastoma of the lower jaw: A rare challenging entity. Dent Res J 2023;20:77

How to cite this URL:
Moradi M, Neville BW, Aminishakib P. Keratoameloblastoma of the lower jaw: A rare challenging entity. Dent Res J [serial online] 2023 [cited 2023 Oct 1];20:77. Available from: https://www.drjjournal.net/text.asp?2023/20/1/77/382130




  Introduction Top


Ameloblastoma is the most common odontogenic epithelial tumor excluding odontoma. This entity is a benign, slow-growing, and locally invasive neoplasm that probably arises from intraosseous remnants of odontogenic tissues.[1] They can occur in either jaw, but the posterior region of the mandible is the most common site. Histopathologically, ameloblastomas typically consist of islands, nests, cords, or strands of odontogenic epithelium rimmed by columnar cells, demonstrating nuclei located in the apical half of the cell body away from the basement membrane (reverse polarity appearance). A wide variety of histologic patterns are recognized, including follicular, cystic, acanthomatous, plexiform, desmoplastic, granular cell, and basal cells.[2],[3]

Acanthomatous change with attempted keratinization may be observed in ameloblastomas, usually in the form of squamous metaplasia of the central stellate reticulum-like cells of the tumor islands.[4] The term “keratoameloblastoma” (KA) has been applied to rare examples of ameloblastoma that exhibit a markedly greater amount of keratin production throughout the tumor. This term was first introduced by Pindborg in 1970, and Altini et al. reported the first verified case.[5],[6]

This article's goal is to describe the clinical, radiological, and histological characteristics of a new instance of KA.


  Case Report Top


In January 2023, a 54-year-old female patient with no significant past medical or dental history was referred to a private dental office with an expansile swelling of the right side of her face. Radiographic examination revealed a well-defined, unilocular lesion with buccal and lingual expansion in the posterior mandible [Figure 1].
Figure 1: Panoramic view shows a well-defined lesion on the posterior area of the right mandibular bone.

Click here to view


The clinicoradiographic differential diagnosis included a “unicystic ameloblastoma” and “developmental odontogenic cysts” - especially odontogenic keratocyst. Then, an excisional biopsy was performed, and the specimen was sent to the pathology laboratory for histological diagnosis.

The gross examination of the specimen showed multiple fragmented pieces of soft gray-brown cyst-like tissue measuring 4 cm × 3 cm × 2 cm in the aggregate, as well as two pieces of bony tissue measuring 1 cm × 1 cm × 0.7 cm.

The tissues were completely embedded, and an odontogenic tumor with cords and nests of odontogenic epithelium inside a dense connective tissue stroma was found during the histological inspection of the H- and E-stained sections. Numerous proliferating follicular islands showed palisaded ameloblast-like cells with prominent reverse nuclear polarity at the periphery. The central epithelium consisted of loosely arranged cells resembling the stellate reticulum of the enamel organ. The low-power magnification showed multiple cystic spaces, which were filled with keratinized material [Figure 2]. High-power examination of the islands showed bland-appearing cells with no evidence of mitotic activity. Therefore, a final diagnosis of “KA” was made. Additional surgical treatment including peripheral ostectomy was performed to minimize the risk of recurrence of the tumor, with a plan for close long-term follow-up.
Figure 2: (a and b) Prominent keratinization at the superficial layers of the epithelium (×100). (c and d) Palisading and reverse polarity at the peripheral columnar cells and stellate-like cells at the central area of the nests (c: ×100 and d: x400).

Click here to view


Furthermore, no evidence of recurrence is observed after 6-month follow-up.


  Discussion Top


Ameloblastoma is a benign, but locally invasive epithelial neoplasm that resembles the enamel organ. In some instances, an aggressive clinicoradiographic presentation of ameloblastoma might be challenging to differentiate from other primary or metastatic neoplasms. Then, microscopic features are often helpful to make a definite diagnosis.[7]

A rare form of ameloblastoma known as “KA” exhibits a keratinization pattern described as showing a lamellar appearance.[8],[9] All reported cases in English literature are summarized in [Table 1]. The World Health Organization (WHO) described histopathologic findings of KA as a separate entity that was described as “ameloblastoma with considerable keratinization” in 1992, although this entity is not included in the most recent WHO classification for odontogenic tumors. Due to keratinization, WHO recognized this lesion as belonging to the histopathological spectrum of “Acanthomatous ameloblastoma.”[15],[17] We believe that beyond the various patterns of ameloblastoma, it is crucial to differentiate KA from other keratin-forming jaw lesions [Table 2].
Table 1: Summary of keratoameloblastoma cases reported in English literature

Click here to view
Table 2: Summary of jaw lesions with keratinization in differential diagnosis with keratoameloblastoma

Click here to view


Intraosseous well-differentiated squamous cell carcinoma should be considered an important differential diagnosis. Significant cellular atypia with pearl-like keratinization and lack of microscopic features of ameloblastoma (such as palisading and reverse polarity at the periphery and stellate-like reticulum at the central area of tumoral nests) can be helpful to rule out variants in ameloblastoma family. In addition, clinicoradiographic findings typically demonstrate an invasive malignant behavior in squamous cell carcinoma.

There are several variations and histologic forms of conventional ameloblastoma, including plexiform, follicular, acanthomatous, basal cell, and granular cell.[16] Acanthomatous ameloblastoma, KA, and the solid variant of odontogenic keratocyst (SOKC) can have similar histologic features, and keratinous material is produced by all three lesions. In acanthomatous ameloblastomas, squamous metaplasia occurs in the central cells of the tumor islands, which sometimes may result in focal overt keratin production. Although this subtype demonstrates common microscopic features of ameloblastoma, including basal cells' palisading and reverse polarity, the degree of keratinization of the neoplastic cells is not as prominent as that observed in KA and SOKC.

To differentiate KA from SOKC, no significant, well-defined criteria have been documented, mostly because of the rarity of SOKC cases. However, the reverse polarity of columnar cells at the periphery and loosely arranged cells resembling the stellate reticulum toward the center of the tumoral nests are not usually observed in SOKC.[10],[22] In addition, OKC with prominent daughter cysts formation may show overlapping features with KA and SOKC.

In conclusion, KA should be recognized as a separate subtype of ameloblastoma (not a separate entity) with distinguishable microscopic features from other cystic/neoplastic lesions of the jaw. In addition, it seems that there is no clinical significance for KA in comparison with other subtypes of solid ameloblastoma.

Consent

The patient noticed that her name and photo will not be published in the report.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given her consent for her images and other clinical information to be reported in the journal. The patient understands that his name and initials will not be published and due efforts will be made to conceal his identity, but anonymity cannot be guaranteed.[26]

Acknowledgment

We would like to thank Dr. Rokni for providing clinical findings.

Financial support and sponsorship

Nil.

Conflicts of interest

The authors of this manuscript declare that they have no conflicts of interest, real or perceived, financial or non-financial in this article.



 
  References Top

1.
Neville BW, Damm DD, Allen CM, Chi AC. Oral and Maxillofacial Pathology. St Louis: Elsevier Health Sciences; 2015.  Back to cited text no. 1
    
2.
Morgan PR. Odontogenic tumors: A review. Periodontol 2000 2011;57:160-76.  Back to cited text no. 2
    
3.
Dandriyal R, Gupta A, Pant S, Baweja HH. Surgical management of ameloblastoma: Conservative or radical approach. Natl J Maxillofac Surg 2011;2:22-7.  Back to cited text no. 3
[PUBMED]  [Full text]  
4.
Gardner D, Heikinheimo K, Shear M, Philipsen H, Coleman H, Leon B, et al. Pathology and Genetics of Head and Neck Tumours (IARC WHO Classification of Tumours). 1st edition. Geneva: World Health Organization, 2005.  Back to cited text no. 4
    
5.
Pindborg JJ. Pathology of the Dental Hard Tissues. Philadelphia: Saunders; 1970.  Back to cited text no. 5
    
6.
Altini M, Lurie R, Shear M. A case report of keratoameloblastoma. Int J Oral Surg 1976;5:245-9.  Back to cited text no. 6
    
7.
Collini P, Zucchini N, Vessecchia G, Guzzo M. Papilliferous keratoameloblastoma of mandible: A papillary ameloblastic carcinoma: Report of a case with a 6-year follow-up and review of the literature. Int J Surg Pathol 2002;10:149-55.  Back to cited text no. 7
    
8.
Takeda Y, Satoh M, Nakamura S, Ohya T. Keratoameloblastoma with unique histological architecture: An undescribed variation of ameloblastoma. Virchows Arch 2001;439:593-6.  Back to cited text no. 8
    
9.
Lee C, Park BJ, Yi WJ, Heo MS, Lee SS, Huh KH. Keratoameloblastoma: A case report and a review of the literature on its radiologic features. Oral Surg Oral Med Oral Pathol Oral Radiol 2015;120:e219-25.  Back to cited text no. 9
    
10.
Altini M, Slabbert HD, Johnston T. Papilliferous keratoameloblastoma. J Oral Pathol Med 1991;20:46-8.  Back to cited text no. 10
    
11.
Siar CH, Ng KH. 'Combined ameloblastoma and odontogenic keratocyst' or 'keratinising ameloblastoma'. Br J Oral Maxillofac Surg 1993;31:183-6.  Back to cited text no. 11
    
12.
Norval EJ, Thompson IO, van Wyk CW. An unusual variant of keratoameloblastoma. J Oral Pathol Med 1994;23:465-7.  Back to cited text no. 12
    
13.
Said-al-Naief NA, Lumerman H, Ramer M, Kopp W, Kringstein GJ, Persenchino F, et al. Keratoameloblastoma of the maxilla. A case report and review of the literature. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1997;84:535-9.  Back to cited text no. 13
    
14.
Kaku T, Ohuchi T, Hattori Y, Nishimura M, Nakade O, Abiko Y. Keratoameloblastoma of the mandible. J Oral Pathol Med 2000;29:812.  Back to cited text no. 14
    
15.
Whitt JC, Dunlap CL, Sheets JL, Thompson ML. Keratoameloblastoma: A tumor sui generis or a chimera? Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2007;104:368-76.  Back to cited text no. 15
    
16.
Adeyemi B, Adisa A, Fasola A, Akang E. Keratoameloblastoma of the mandible. J Oral Maxillofac Pathol 2010;14:77-9.  Back to cited text no. 16
[PUBMED]  [Full text]  
17.
Sisto JM, Olsen GG. Keratoameloblastoma: Complex histologic variant of ameloblastoma. J Oral Maxillofac Surg 2012;70:860-4.  Back to cited text no. 17
    
18.
Ketabi MA, Dehghani N, Sadeghi HM, Shams MG, Mohajerani H, Azarsina M, et al. Keratoameloblastoma, a very rare variant of ameloblastoma. J Craniofac Surg 2013;24:2182-6.  Back to cited text no. 18
    
19.
Mohanty N, Rastogi V, Misra SR, Mohanty S. Papilliferous keratoameloblastoma: An extremely rare case report. Case Rep Dent 2013;2013:706128.  Back to cited text no. 19
    
20.
Raj V, Chandra S, Bedi RS, Dwivedi R. Keratoameloblastoma: Report of a rare variant with review of literature. Dent Res J (Isfahan) 2014;11:610-4.  Back to cited text no. 20
    
21.
Bedi RS, Sah K, Singh A, Chandra S, Raj V. Keratoameloblastoma or kerato-odontoameloblastoma: Report of its soft tissue recurrence with literature review. Quant Imaging Med Surg 2015;5:898-908.  Back to cited text no. 21
    
22.
Palaskar SJ, Pawar RB, Nagpal DD, Patil SS, Kathuriya PT. Keratoameloblastoma a rare entity: A case report. J Clin Diagn Res 2015;9:D05-7.  Back to cited text no. 22
    
23.
Konda P, Bavle RM, Muniswamappa S, Makarla S, Venugopal R. Papilliferous keratoameloblastoma of the mandible – A rare case report. J Clin Diagn Res 2016;10:D08-11.  Back to cited text no. 23
    
24.
Prabhakar M, Sivapathasundharam B, Logeswari J, Manikandhan R. Keratoameloblastoma of oral cavity: Report of two cases. Medico Leg Update 2020;20:2248-54.  Back to cited text no. 24
    
25.
Kuberappa PH, Anuradha A, Kiresur MA, Bagalad BS. Papilliferous keratoameloblastoma – A rare entity: A case report with a review of literature. J Oral Maxillofac Pathol 2020;24:S2-6.  Back to cited text no. 25
    
26.
Robinson L, Smit C, Fonseca FP, Abrahão AC, Romañach MJ, Khurram SA, et al. Keratoameloblastoma: A report of seven new cases and review of literature. Head Neck Pathol 2022;16:1103-13.  Back to cited text no. 26
    


    Figures

  [Figure 1], [Figure 2]
 
 
    Tables

  [Table 1], [Table 2]



 

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
Case Report
Discussion
References
Article Figures
Article Tables

 Article Access Statistics
    Viewed396    
    Printed38    
    Emailed0    
    PDF Downloaded52    
    Comments [Add]    

Recommend this journal