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


 
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CASE REPORT  
Year : 2012  |  Volume : 16  |  Issue : 1  |  Page : 113-117
 

Squamous odontogenic tumor: A case report and review of literature


Department of Oral and Maxillofacial Pathology, Dr. Syamala Reddy Dental College, Hospital and Research Centre, Bangalore, India

Date of Web Publication17-Feb-2012

Correspondence Address:
Manjunath Badni
Department of Oral Pathology and Microbiology, Sardar Patel Post Graduate Institute of Dental and Medical Sciences, Chaudhary Vihar, Raebareli Road, Lucknow 226 025, Uttar Pradesh
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0973-029X.92986

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   Abstract 

The squamous odontogenic tumor (SOT) is a rare, benign, locally infiltrative neoplasm of the jaws that appears to originate from the rests of Malassez, gingival surface epithelium or from remnants of the dental lamina. SOT was first described by Pullon et al. (1975). Since then there has been paucity in the number of reported cases, especially in the Indian subcontinent. The tumor is often asymptomatic, although it can present with symptoms of pain and tooth mobility. The characteristic radiographic appearance is that of a triangular-shaped unilocular radiolucency associated with the roots of erupted, vital teeth and has a predilection for the anterior maxilla and the posterior mandible. Histologically, the tumor is characterized by the formation of variably sized nests and cords of uniform, benign-appearing, squamous epithelium with occasional vacuolization and keratinization. We report a case of SOT occurring in a 58-year-old male in the anterior mandible with unusual localization and appearance.


Keywords: Odontogenic tumor, rests of Malassez, squamous cells


How to cite this article:
Badni M, Nagaraja A, Kamath V V. Squamous odontogenic tumor: A case report and review of literature. J Oral Maxillofac Pathol 2012;16:113-7

How to cite this URL:
Badni M, Nagaraja A, Kamath V V. Squamous odontogenic tumor: A case report and review of literature. J Oral Maxillofac Pathol [serial online] 2012 [cited 2019 Sep 22];16:113-7. Available from: http://www.jomfp.in/text.asp?2012/16/1/113/92986



   Introduction Top


Squamous odontogenic tumor (SOT) is a lesion which had been recognized as an apparent entity for a number of years until 1975, when Pullon and coworkers published a series of six cases. [1] SOT has been defined as a benign but locally infiltrative neoplasm consisting of islands of well-differentiated squamous epithelium in a fibrous stroma. The epithelial islands occasionally show foci of central cystic degeneration. [2] SOT is a rare, benign but locally infiltrative epithelial tumor that supposedly develops from the remnants of dental lamina, or of the cell rests of Malassez (ROM), or gingival epithelium. [3]

To date, fewer than 50 cases have been reported in the literature. The most common site of occurrence of the lesion in the mandible is the bicuspid-molar region and in the maxilla, incisor-cuspid area. Radiographically, SOT often exhibits a characteristic unilocular and triangular-shaped radiolucency of the alveolar bone, with the wide base of the radiolucency localized between the diverging apices of the adjacent roots. [4] Histologically, the tumor is characterized by multiple islands of squamous epithelium surrounded by a mature connective tissue stroma. Cystic degeneration or calcification may occasionally be observed in the epithelial islands. [5] The usual treatment has been simple enucleation and recurrence has been rare. [6] The purpose of this article is to report a new case and review the literature.


   Case Report Top


A 58-year-old male patient reported to our dental hospital with a complaint of swelling and mobility of teeth in the right anterior region of mandible from past 3 months. Onset occurred 3 months ago and it was asymptomatic. Medical history of patient was unremarkable. Clinical examination revealed a firm anterior swelling in right central and lateral incisor region of mandible. The mandibular right central incisor and canine were mobile. Radiograph [Figure 1] showed radiolucency with severe alveolar bone loss localized between right lateral and central incisor region of mandible, which was associated with markedly diverging roots. Based on the clinical and radiographic findings, the initial diagnosis of periodontosis was made and subjected for histologic examination. Histological examination [Figure 2],[Figure 3] and [Figure 4] revealed a proliferation of mature stratified squamous epithelial islands in a dense fibrous connective stroma and the diagnosis of SOT was confirmed.
Figure 1: Panoromic radiograph reveals triangular radiolucent area involving roots of mandibular right central and lateral incisor

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Figure 2: Photomicrograph revealing scattered islands of squamous epithelium in a dense fibrous connective tissue stroma (H and E, stain ×4 magnification)

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Figure 3: Photomicrograph revealing an island of benign squamous epithelium without presence of peripheral columnar cells, palisading nuclei or stellate reticulum (H and E, stain ×10 magnification)

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Figure 4: Photomicrograph of an epithelial island composed of uniform squamous epithelial cells (H and E, stain ×40 magnification)

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   Discussion Top


After Pullon et al. had described an entity named SOT, a number of additional cases have been reported in the literature. [3] To date, 44 cases of SOT have been reported [Table 1]. Due to the paucity of documented cases of SOT, the relative frequency among odontogenic tumors cannot be stated. [2] SOT is known to occur in a wide age range, from first decade to eighth decade of life, with mean age of occurrence being 38.2 years. The gender ratio among 44 cases being 1:1.8 (F:M) showing slightly more predilection among males [Table 1].
Table 1: Summary of reported cases of SOT

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Out of the 44 cases excluding our case, 20 have been located in posterior region of mandible. In maxilla, SOT occurred most commonly in canine-first premolar area. [7] Our case is unique in that it is the first case reported in the Indian literature and second ever case to occur between the roots of central and lateral incisors in the anterior segment of the mandible. Hence, the most common location for development of an SOT in the maxilla is anterior region and posterior in case of mandible with almost equal propensity to occur in both the jaws. [7] SOTs occurring in maxilla were found to be more aggressive than in mandible. [2],[6] This was mainly due to the anatomy, porous and medullary nature of bone. [8] Leider et al. reported a rare familial tendency for this neoplasm. [9]

Most of the cases arise and develop in the periodontium of permanent dentition. One case was associated with the deciduous dentition and four cases were detected in edentulous areas. [2],[3],[5]

Clinical presentation of SOTs represented a slow growing, intrabony lesion with very few clinical signs and symptoms. Most common being mobility of adjacent teeth, swelling of alveolar process, and mild/moderate pain in the affected areas. However, lesion may be asymptomatic and detected in routine intraoral radiographs. [8]

Radiograph of common central variant of SOT shows a well-defined unilocular, triangular radiolucency between the roots of adjacent teeth. Root resorption, radiopacities seen in other odontogenic neoplasms are seldom a feature of SOT. Large and extensive SOTs may, however, show multilocular pattern. Root resorption was noticed in only one case. [10] The peripheral variant may cause some saucerization of underlying bone. This was likely to be a pressure phenomenon rather than the result of true tumor infiltration. [2]

Histologically, the lesion usually presents as islands of benign squamous epithelium in mature connective tissue stroma without the evidence of peripheral columnar cells, palisading nuclei, or stellate reticulum. The epithelial islands of SOT seem to resemble the squamous metaplasia seen in ameloblastoma; however, the lack of peripheral columnar cells and palisading nuclei establishes the differential diagnosis between these two tumors. Moreover, it must be distinguished from primary intraosseous squamous cell carcinoma, which is rare in young persons and presents dysplastic epithelial features. [11] Keratin pearls, microcysts, and intraepithelial calcification are often present in SOTs. Circular areas of fibroblast and fibrous condensation/hyalinization can be seen around some of the epithelial islands, which suggests a connective tissue reaction to epithelial proliferation. [7]

In one of the reported cases, electron microscopy showed epithelial cells with features similar to cells of stratum spinosum with numerous desmosomes, abundant glycogen granules, tonofilaments, and myelin bodies. [12]

The pathogenesis of SOT has yet remained unclear. The epithelial odontogenic tumors are histologically related to remnants of odontogenic epithelium, which includes the dental lamina (cell rests of Serre), enamel organ, and the root sheath of Hertwig (cell ROM). Actively growing dental lamina is present within the jaws for a considerable time after birth. Because of the widespread presence of odontogenic epithelium, some tumors may arise from residues of these cells in bone or in soft tissues such as the gingiva. Regarding the pathogenesis of SOT, most researchers have pointed toward a periodontal ligament origin for the central variant of the lesion. Radiographic appearance of the lesion, occurring between the adjacent teeth in the tooth bearing area from the periodontal ligament space, and the pattern of bone destruction seeming to emanate relatively uniformly from the areas of tooth roots lend credence to the theory of origin from the periodontal ligament, viz., from the ROM. Microscopic findings, the epithelial islands which are intimately associated with the apices of the retained teeth, and tight adherence of tumor mass to the canine and ease of separation from the buccal soft tissue further add to the notion of origin from ROM. The ROM hitherto considered to be resting cells in the periodontal ligament have received much of attention recently. It is known that the ROM persists into adult life in all areas of the periodontal ligament but most abundantly in the area of the cervical half of the root where some have even proliferated and formed structures within the periodontal ligament similar to rests of Serre. The fact that some cases are reported in edentulous areas does not take away the possibility that they originated from ROM of teeth formerly present. [4],[9]

The heightened activity in nonperiodontal lesions can perhaps be attributed to certain genetic etiologies. The ameloblastin gene, for example, has been shown to express an important protein in epithelial-mesenchymal signaling during odontogenesis, and mutations of this gene have been found in SOT, Adenomatoid Odontogenic Tumor and Ameloblastomas. Further investigations need to be done to see if mutations in this gene have a vital role in tumorigenesis of SOT. In addition, the heparanase gene, which codes for an enzyme that is important in dissemination and cellular invasion, is prevalent in ameloblastomas. The production of heparanase was thought to contribute to its local invasiveness. Further studies with heparanase in other locally invasive lesions such as SOTs can perhaps be performed to establish additional genetic influences related to the aggressiveness of some of SOTs reported recently. [7]

Carr et al. postulated a gingival origin for the SOTs and observed that the insular growth pattern of the tumor, the presence of squamous cells with clear cytoplasm, the parakeratosis, and the tendency to microcyst formation were related to gingival rests of Serres. [10]

Proliferation of squamous epithelial islands in SOT has also been reported in submucosal regions, which might indicate that the lesion originates from the rests of Serres. However, it should be recognized that there are peripheral variants of SOT that are thought to arise from gingival surface epithelium or from remnants of the dental lamina (rests of Serres). [10]

SOT-like proliferations (SOT-LP) have been reported in fewer than 15 cases, arising from the walls of the odontogenic cysts. These lesions were cystic by nature, although histologically were similar to SOT, they exhibited no tendency to evolve into neoplasms. SOT-LP exhibited varying clinical, radiological, and prognostic features than true SOTs. Biologically, SOTs are less aggressive than ameloblastomas but are more aggressive than SOT-LP in the cysts, except for those arising from the walls of odontogenic keratocysts. [9]

Immunohistochemical studies conducted by Tatemoto et al. and Yamada et al. on SOT confirmed the proliferative activity of odontogenic epithelium indicated by heavy staining for keratin 13/16, and squamous differentiating cells in the center of tumor islands have shown a strong positive reaction for involucrin staining. [13],[14]

Treatment of SOT involves conservative local excision, curettage, enucleation, and scaling of adjacent teeth. [2],[8] Recurrences have been reported in only one case, most likely due to insufficient initial removal. [8]

Ide et al. suggested that SOT could transform into a malignant disorder such as intraosseous squamous cell carcinoma. [17] King Kim et al. suggested that SOT can decorticate the dense bone of mandible and may impact the therapeutic modalities and diagnosis management of these presumed innocuous lesion. [7]

SOT is a benign odontogenic neoplasm of distinctive histological features probably arising from ROM, although three decades have passed since the establishment of the lesion as a separate entity much remains to be learned about the SOT. The sporadic reports in the literature belie the propensity of the lesion to occur in the jaws. A probable reason could be the comparative few reports and the common mistaken diagnosis of an acanthomatous ameloblastoma.[31]

 
   References Top

1.Rajendran R. Cyst and Tumors of Odontogenic Origin. In: Rajendran R, Sivapathasundharam B, editors. Shafer's Text Book of Oral Pathology, 5 th ed. Noida: Elservier; 2005. p. 398-400.  Back to cited text no. 1
    
2.Philipsen HP, Reichart PA. Squamous odontogenic tumor (SOT): A benign neoplasm of the periodontium A review of 36 reported cases. J Clin Periodontol 1996;23:922-6.  Back to cited text no. 2
    
3.Pullon PA, Shafer WG, Elzay RP, Kerr DA, Corio RL. Squamous odontogenic tumour. Report of six cases of a previously undescribed lesion. Oral Surg Oral Med Oral Pathol 1975;40:616-30.  Back to cited text no. 3
    
4.Haghighat K, Kalmar JR, Mariotti AJ. Squamous odontogenic tumor: Diagnosis and management. J Periodontol 2002;73:653-6.  Back to cited text no. 4
    
5.Schwartz-Arad D, Lustmann J, Ulmansky M. Squamous odontogenic tumour. Review of literature and case report. Int J Oral Maxillofac Surg 1990;19:327-30.  Back to cited text no. 5
    
6.Baden E, Doyle J, Mesa M, Fabié M, Lederman D, Eichen M. Squamous odontogenic tumour. Report of three cases including the first extraosseous case. Oral Surg Oral Med Oral Pathol 1993;75:733-8.  Back to cited text no. 6
    
7.Kim K, Mintz SM, Stevens J. Squamous odontogenic tumour causing erosion of the lingual cortical plate in the mandible: A report of 2 cases. J Oral Maxillofac Surg 2007;65:1227-31.  Back to cited text no. 7
    
8.Barrios TJ, Sudol JC, Cleveland DB. Squamous odontogenic tumor associated with an erupting maxillary canine: Case report. J Oral Maxillofac Surg 2004;62:742-4.  Back to cited text no. 8
    
9.Leider AS, Jonker LA, Cook HE. Multicentric familial squamous odontogenic tumour. Oral Surg Oral Med Oral Pathol 1989;68:175-81.  Back to cited text no. 9
    
10.Carr RF, Carlton DM Jr, Marks RB. Squamous odontogenic tumor: Report of case. J Oral Surg 1981;39:297-8.  Back to cited text no. 10
    
11.Favia GF, Di Albert L, Scarano A, Piattelli A. Squamous odontogenic tumour: Report of two cases. Oral Oncol 1997;33:451-3.  Back to cited text no. 11
    
12.McNeill J, Price HM, Stoker NG. Squamous odontogenic tumor: Report of case with long-term history. J Oral Surg 1980;38:466-71.  Back to cited text no. 12
    
13.Tatemoto Y, Okada Y, Mori M. Squamous odontogenic tumor: Immunohistochemical identification of keratins. Oral Surg Oral Med Oral Pathol 1989;67:63-7.  Back to cited text no. 13
    
14.Yamada K, Tatemoto Y, Okada Y, Mori M. Immunostaining of involucrin in odontogenic epithelial tumors and cysts. Oral Surg Oral Med Oral Pathol 1989;67:564-8.  Back to cited text no. 14
    
15.Ruhin B, Raoul G, Kolb F, Casiraghi O, Lecomte-Houcke M, Ghoul S, et al. Aggressive maxillary squamous odontogenic tumour in a child: Histological dilemma and adaptive surgical behavior. Int J Oral Maxillofac Surg 2007;36:864-6.  Back to cited text no. 15
    
16.Kim JY, Kim JC, Cho BO, Kim SG, Yang BE, Rataru H. Squamous odontogenic tumor: A case report and review of literature. J Korean Assoc Oral Maxillofac Surg 2007;33:59-2.  Back to cited text no. 16
    
17.Ide F, Shimoyama T, Horie N, Shimizu S. Intraosseous squamous cell carcinoma arising in association with a squamous odontogenic tumour of the mandible. Oral Oncol 1999;35:431-4.  Back to cited text no. 17
    
18.Doyle JL, Grodjesk JE, Dolinsky HB, Rafel SS. Squamous odontogenic tumor: Report of three cases. J Oral Surg 1977;35:994-6.  Back to cited text no. 18
    
19.Hopper TL, Sadeghi EM, Pricco DF. Squamous odontogenic tumor: Report of a case with multiple lesions. Oral Surg Oral Med Oral Pathol 1980;50:404-10.  Back to cited text no. 19
    
20.Leventon GS, Happonen RP, Newland JR. Squamous odontogenic tumor. Am J Surg Pathol 1981;5:671-7.  Back to cited text no. 20
    
21.Kangvonkit P, Sirichitra V, Hansasuta C. Squamous odontogenic tumor (report of a case and review of the literature). J Dent Assoc Thai 1981;31:25-33.  Back to cited text no. 21
    
22.Goldblatt LI, Brannon RB, Ellis GL. Squamous odontogenic tumor: Report of five cases and review of the literature. Oral Surg Oral Med Oral Pathol 1982;54:187-96.  Back to cited text no. 22
    
23.Cataldo E, Less WC, Giunta JL. Squamous odontogenic tumor: A lesion of the periodontium. J Periodontol 1983;54:731-5.  Back to cited text no. 23
    
24.Swan RH, McDaniel RK. Squamous odontogenic proliferation with probable origin from the rests of Malassez (early squamous odontogenic tumor?). J Periodontol 1983;54:493-6.  Back to cited text no. 24
    
25.Norris LH, Baghaei-Rad M, Maloney PL, Simpson G, Guinta J. Bilateral maxillary squamous odontogenic tumor and the malignant transformation of a mandibular radiolucent lesion. J Oral Maxillofac Surg 1984;42:827-34.  Back to cited text no. 25
    
26.Kristensen S, Andersen J, Jacobsen P. Squamous odontogenic tumor: Review of literature and a new case. J Laryngol Otol 1985;99:919-24.  Back to cited text no. 26
    
27.Monteil RA, Terestri P. Squamous odontogenic tumor related to an unerupted lower canine. J Oral Maxillofac Surg 1985;43:888-95.  Back to cited text no. 27
    
28.Warnock GR, Pierce GL, Correll RW, Baker DA. Triangular-shaped radiolucent area between roots of the mandibular right canine and first premolar. J Am Dent Assoc 1985;110:945-6.  Back to cited text no. 28
    
29.Mills WP, Davila MA, Beuttenmuller EA, Koudelka BM. Squamous odontogenic tumor: Report of a case with lesions in three quadrants. Oral Surg Oral Med Oral Pathol 1986;61:557-63.  Back to cited text no. 29
    
30.Yaacob HB. Squamous odontogenic tumor. J Nihon Univ Sch Dent 1990;32:187-91.  Back to cited text no. 30
    
31.Saxby MS, Rippin JW, Sheron JE. Case report: Squamous odontogenic tumor of the gingiva. J Periodontol 1993;64:1250-2.  Back to cited text no. 31
    


    Figures

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

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