Odontogenic fibroma (OF) is a rare benign odontogenic neoplasm that is most commonly found in the mandibular/
premolar region of female patients in the second to fourth decades of life. Well-defined radiolucent lesions that
may induce root resorption are normally observed. Rare variants of OF have been described in the prior literature,
including references to: 1) giant cell lesions, 2) amyloid-like protein deposition, and 3) ossifying variants. Immuno
-
histochemistry can contribute to understanding the biological behavior and the pathogenesis of OF. Therefore, this
case report aimed to describe a new case of ossifying OF and discuss the histopathology and immunohistochemical
features

Amaral, Márcio Bruno Figueiredo

Gomez, Ricardo Santiago

Horta, Martinho Campolina Rebello

Mesquita, Ricardo Alves

Souto, Giovanna Ribeiro

Journal of Clinical and Experimental Dentistry

PubMed

Repositori d'Objectes Digitals per a l'Ensenyament la Recerca i la Cultura

J Clin Exp Dent. 2014;6(5):e588-91.                                                                                                                                                                                      Ossifying odontogenic fibromae588Journal section: Oral Medicine and Pathology                         Publication Types: Case ReportOssifying odontogenic fibroma: A rare case reportMárcio-Bruno-Figueiredo Amaral 1, Giovanna-Ribeiro Souto 1, Martinho-Campolina-Rebello Horta 2, Ricardo-Santiago Gomez 1, Ricardo-Alves Mesquita 11 Department of Oral Surgery and Pathology. School of Dentistry. Universidade Federal de Minas Gerais. Belo Horizonte - MG, Brazil2  Department of Dentistry, Pontifícia Universidade Católica de Minas Gerais. Belo Horizonte - MG, BrazilCorrespondence:Universidade Federal de Minas GeraisFaculdade de OdontologiaAv. Antônio Carlos, 6667 sala 3202-DPampulhaBelo Horizonte - MG, Brasil31.270-901marciobrunoamaral@gmail.comReceived: 27/12/2013Accepted: 12/06/2014Abstract Odontogenic fibroma (OF) is a rare benign odontogenic neoplasm that is most commonly found in the mandibular/premolar region of female patients in the second to fourth decades of life. Well-defined radiolucent lesions that may induce root resorption are normally observed. Rare variants of OF have been described in the prior literature, including references to: 1) giant cell lesions, 2) amyloid-like protein deposition, and 3) ossifying variants. Immuno-histochemistry can contribute to understanding the biological behavior and the pathogenesis of OF. Therefore, this case report aimed to describe a new case of ossifying OF and discuss the histopathology and immunohistochemical features.Key words: Odontogenic fibroma, jaw tumors, ossifying variant.doi:10.4317/jced.51440http://dx.doi.org/10.4317/jced.51440Article Number: 51440                http://www.medicinaoral.com/odo/indice.htm© Medicina Oral S. L. C.I.F. B 96689336 - eISSN: 1989-5488eMail:  jced@jced.esIndexed in:PubmedPubmed Central® (PMC)ScopusDOI® SystemAmaral MBF, Souto GR, Horta MCR, Gomez RS, Mesquita RA. Ossifying odontogenic fibroma: A rare case report. J Clin Exp Dent. 2014;6(5):e588-91.http://www.medicinaoral.com/odo/volumenes/v6i5/jcedv6i5p588.pdfIntroductionOdontogenic fibroma (OF) is a rare benign odontogenic neoplasm. Clinically, OF is most common in the mandi-bular/premolar region of female patients in the second to fourth decades of life and is frequently found as radiolu-cent lesions that may induce root resorption (1).Histopathologically, OF is characterized by variable amounts of inactive-looking odontogenic epithelium em-bedded in a mature fibrous connective tissue stroma (2). Although odontogenic epithelial rests does not define the diagnosis, these structures must be observed to reach a diagnosis of OF (3).The cytokeratin (CK) expression may well be a useful tool to confirm the diagnosis of OF in epithelium-poor cases and to reveal the main types expressed in the OF when compared to other odontogenic tumors (3). Rare variants of OF have been described in prior literature including references to: 1) with giant cell lesions, 2) amyloid-like protein deposition, and 3) ossifying va-riant (4).Therefore the present study is aimed to describe a rare case of ossifying odontogenic fibroma and discuss the histopathology and immunohistochemical features of this rare variant of OF.J Clin Exp Dent. 2014;6(5):e588-91.                                                                                                                                                                                      Ossifying odontogenic fibromae589Case ReportA 43-year-old woman with noncontributory medical, so-cial, and cultural records was referred to the Oral and Maxillofacial Surgery Service, Department of Dentis-try, Pontifícia Universidade Católica de Minas Gerais in Belo Horizonte, Brazil, to evaluate a nodule in her mouth. The patient reported that the lesion had been pre-senting a slow progressive growth for 3 years. Through clinical examination, a swelling of the left paranasal area with asymmetry could be observed extraorally. In-traorally, a swelling of the left maxilla associated with teeth 21, 22, and 25 could be identified. Teeth 23 and 24 were not presented. The lesion was painless, uneventful, well-defined, firm consistency, covered by normal color and texture of mucosa, and measured 32 x 30 mm. The cone-beam computed tomography (CBCT) of the maxi-lla showed a well-defined mixed hyperdense/hypodense lesion (Fig. 1a,c). Expansion of the buccal cortical bone (Fig. 1a,d), as well as root resorption on teeth 21 and 22 (Fig. 1b), could be observed. Additionally, expansion of the lateral wall, associated with invasion of the na-sal cavity, could be identified by CBCT imagery (Fig. 1a,c). Ossifying fibroma, calcifying epithelial odontoge-nic tumor, calcifying cystic odontogenic tumor, complex odontoma, dentinogenic ghost cell tumor, and adenoma-toid odontogenic tumor were proposed as differential cli-nical-radiographic diagnoses. An incisional biopsy was performed and a suggestive histopathological diagnosis of the ossifying fibroma was proposed. Enucleation of the lesion was performed by intraoral approach. An im-portant surgical finding was the easy detachment of the lesion from the healthy bone. Microscopical analysis of Fig. 1. Cone beam computed tomography (CBCT) features of os-sifying variant of odontogenic fibroma. a) Axial plane showing a mixed hyperdense-hypodense image with buccal expansion in the left maxilla. b) Coronal plane showing root resorption of tee-th 21 and 22. c) In the parasagital plane, a mixed image measu-ring 32.5 mm associated with a hypodense line (red arrows red) delimiting the lesion of the health bone. d) 3D-CBCT showing buccal expansion of the lesion associated with invasion of the nasal cavity.surgical piece demonstrated a lesion with fibroosseous features, comprised of composed by mature collagenous fibers and spindle-shaped fibroblasts, with numerous is-lands and cords of odontogenic epithelium (Fig. 2a,c). This component was intimately admixed with calcified tissue characterized by trabeculae of bone and round shaped structures (Fig. 2b). Immunohistochemical study was performed by employing anti-CK antibodies. Posi-tivity to CK 14 and 19, as well as negativity to CK 7, 8, and 18, could be observed (Fig. 2d). The diagnosis of ossifying OF was therefore established. The posto-perative period proved to be uneventful. The patient is currently undergoing routine follow-up with no signs of recurrence after 12 months.Fig. 2. Histopathological and immunohistochemical features of os-sifying variant of odontogenic fibroma. a) odontogenic fibroma de-monstrates cellular fibroblastic connective tissue with numerous is-lands and cords of odontogenic epithelium. Reactive bone formation involves the lesion (haematoxylin and eosin (HE staining, 40x origi-nal magnification). b) Abundant calcified structures and presence of surrounding conjunctive tissue. c) Islands and cords of odontogenic epithelium, fibroblastic connective tissue and bone formation (HE, 100x original magnification). d) Immunohistochemical staining positive for CK14 in islands and cords of odontogenic epithelium (streptavidin-biotin, 400x original magnification).DiscussionOF is a very rare benign odontogenic tumor. According to the prior literature, OF represents 0 to 5.5% of all odontogenic tumors (3). Although OF has been identified in a wide range of ages, it is most frequently diagnosed in patients between the second to fourth decades of life (5). There is a female predilection for female patients with a female/male ratio of 2.8/1 (2). These data are in accordance with the current case report, which occurred in a 43 year-old female patient. of 43 years of age.Topographically, OF more commonly affects the premo-lar region of the mandible and the anterior region of the maxilla (5,6). Clinically, OF is characterized by an as-ymptomatic slow growth, which results in cortical expan-J Clin Exp Dent. 2014;6(5):e588-91.                                                                                                                                                                                      Ossifying odontogenic fibromae590sion (7). In the present case, the lesion was found in the anterior region of the maxilla with asymptomatic growth and cortical expansion, as reported in prior literature.Considering only cases of ossifying OF in prior literatu-re, three cases were more frequently reported in female patients in the fourth decade of life (4,8).Conventional radiographs, fan-beam computed tomo-graphy or CBCT of OF predominantly shows unilocu-lar or multilocular radiolucent images with well-defined margins (9,10). Ikeshima and Utsumomiya (2005) (11) attempted to show specific characteristics of OF for di-fferential diagnoses, such as well-defined limits, root resorption, and calcification and demonstrated varying characteristics for points such as shape, inner lesion, boundary, bone expansion, and root resorption.Specific radiographic features for OF have yet to be cla-rified; however, severe effects on the surrounding bone trabeculae are often seen, even if the borders are well-defined in radiographic images. Diagnosis of OF should be complicated by several reasons, such as the diversity of radiographic and histopathological characteristics (5). Moreover, the occurrence of calcified material can produ-ce a mixed radiolucent/radiopaque image (2). Therefore, differential diagnosis of ossifying odontogenic fibroma should be made considering benign tumor lesions with these specific image findings such as ossifying fibroma, calcifying epithelial odontogenic tumor, calcifying cys-tic odontogenic tumor, complex odontoma, dentinogenic ghost cell tumor, and adenomatoid odontogenic tumor. Ossifying fibroma should be considered as the main di-fferential diagnosis due to similar fibroosseous mixed radiographic findings found in some cases of OF that could induce a misdiagnosis. Furthermore, large lesions can induce root resorption in the involved teeth and cor-tical expansion (12). In the current case report, a well-defined exuberant hyperdense image could be observed around the hypodense area. In addition, a hypodense line could be observed around the lesion which may well ex-plain the easy detachment of the lesion from the healthy bone. As reported in prior literature, root resorption and bone expansion were also present.Histologically, OF is defined as an odontogenic tumor consisting of a moderately cellular fibrogenic prolifera-tion with monomorphic fibroblastic cells and a thin ma-ture collagen admixed with epithelial cords and islands of odontogenic origin (2). According to findings from Mosqueda-Taylor et al. (3), the immunohistochemical analysis of the epithelial component of the reported OF demonstrates positivity for CK14 and CK19, and negati-vity for CK7, CK8, and CK18. Studies in human enamel organ, as well as in the remnants of the dental lamina, showed that these epithelial cells are positive for CKs 7, 13, 14, and 19, and proved negative for CKs 8, 10, 16, 17, and 18 (13). The remnants of the dental lamina are specifically labeled for CK 7, while the lack of CK7 in some calcifying epithelial odontogenic tumors appears to be related to tumoral indifferentiation (14). Differen-ces in concerning specific state of differentiation were observed only for CKs 14 and 19 in the inner enamel epithelium. An intense immunostaining for CK 14 was present in the inner dental epithelium at the early bell stage, which was substituted by CK 19 at the late bell sta-ge when the ameloblasts were fully differentiated (13). In the present case, islands of odontogenic epithelium demonstrating positivity for CK 14 and 19, which may occur in order to aid in the diagnosis and demonstrate a terminal odontogenic differentiation of the epithelium of ossifying OF. This result was also demonstrated by Eversole et al. (4).Considering the histological differential diagnosis, this lesion showed the typical fibroosseous microscopic fea-tures of an ossifying fibroma. This marked feature pro-bably induces a misdiagnosis of a fibroosseous lesion after incisional biopsy. Therefore, immunohistochemi-cal studies should be performed to clarify the diagnosis when the odontogenic epithelium has been associated with ossifications. The OF is considered a rare lesion, but information suggests that it can also be considered a distinct lesion. It is important to highlight that a re-view of the prior literature demonstrated only four cases of ossifying variants of OF, including this present case report. Therefore, it is important to note that new case reports regarding OF with ossifications are important in an attempt to better define this rare OF variant and des-cribe its clinical, radiographic, and histological features, as well as its biological behavior.References1. Brannon RB. Central odontogenic fibroma, myxoma (odontogenic myxoma, fibromyxoma), and central odontogenic granular cell tumor. Oral Maxillofac Surg Clin North Am. 2004;16:359-74.2. Philipsen HP, Reichart PA, Sciubba JJ, van der Waal I. Odontogenic fibroma. In: Barnes L, Eveson JW, Reichart P, Sidransky D, editors. World Health Organization Classification of Tumours. Pathology and Genetics of Head and Neck Tumours.Lyon: IARC Publishing Group, 2005;315.3. Mosqueda-Taylor A, Martínez-Mata G, Carlos-Bregni R, Vargas PA, Toral-Rizo V, Cano-Valdéz AM, et al. Central odontogenic fibroma: new findings and report of a multicentric collaborative study. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2011;112:349-58.4. Eversole LR. Odontogenic fibroma, including amyloid and ossi-fying variants. Head and Neck Pathol. 2011;5:335-43.5. Kaffe I, Buchner A. Radiologic features of central odontoge-nic fibroma. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1994;78:811-8.6. Raubenheimer EJ, Noffke CE. Central odontogenic fibroma-like tu-mors, hypodontia, and enamel dysplasia: review of the literature and report of a case. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2002;94:74-7. 7. Daniels JS. Central odontogenic fibroma of mandible: a case report and review of the literature. Oral Surg Oral Med Oral Pathol Oral Ra-diol Endod. 2004;98:295-300.8. Araki M, Nishimura S, Matsumoto N, Ohnishi M, Ohki H, Ko-miyama K. Central odontogenic fibroma with osteoid formation showing atypical radiographic appearance. Dentomaxillofac Radiol. 2009;38:426-30.J Clin Exp Dent. 2014;6(5):e588-91.                                                                                                                                                                                      Ossifying odontogenic fibromae5919. Covani U, Crespi R, Perrini N, Barone A. Central odontogenic fibroma: a case report. Med Oral Patol Oral Cir Bucal. 2005;10:e154-7.10. Daskala I, Kalyvas D, Kolokoudias M, Vlachodimitropoulos D, Alexandridis C. Central odontogenic fibroma of the mandible: a case report. J Oral Sci. 2009;51:457-61.11. Ikeshima A, Utsumomiya T. Case report of intra-osseous fibroma: a study on odontogenic and desmoplastic fibromas with a review of the literature. J Oral Sci. 2005;47:149-57.12. Hara M, Matsuzaki H, Katase N, Yanagi Y, Unetsubo T, Asaumi J, et al. Central odontogenic fibroma of the jawbone: 2 case reports des-cribing its imaging features and an analysis of its DCE-MRI findings. Oral Surg Oral Med Oral Pathol Oral Radiol. 2012;113:e51-8.13. Domingues MG, Jaeger MMM, Araújo VC, Araújo NS. Expression of cytokeratins in human enamel organ. Eur J Oral Sci. 2000;108:43-7.14. Crivelini MM, Araújo VC, de Souza SOM, Araújo NS. Cytokera-tins in epithelia of odontogenic neoplasms. Oral Dis. 2003;9:1-6.

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