Abstract
Lesions of non-endodontic origin may mimic periapical abscess. Osteosarcoma is a rare malignant lesion.
Case report
The present report describes a case of chondroblastic osteosarcoma in the periapical region of teeth #29, #30, and #31 of an 18-year-old male. Clinical history showed self-reported discomfort in the right posterior gingiva for over a month. Physical examination showed a small expansion and redness of the right mandibular buccal and lingual cortical plates, but no signs of pain or inflammation were observed. All the teeth responded positively to pulp sensibility. Periapical and panoramic radiographs showed slight periapical radiolucency in the roots of teeth #29 and #30, clear periodontal ligament space widening, and evident loss of lamina dura. Incisional biopsy was performed, and based on microscopic findings the diagnosis of chondroblastic osteosarcoma was confirmed.
Conclusions
Non-endodontic diseases associated with tooth root apex, such as chondroblastic osteosarcoma, should be included in differential diagnosis of jaw lesions that resemble periapical abscess.
Osteosarcoma; Periapical abscess; Apical periodontitis; Differential diagnosis; Endodontics
Introduction
A periapical radiolucency associated with a vital tooth constitutes a diagnostic challenge22 - Bregni RC, Contreras E, Hiraki KR, Vargas PA, León JE, Almeida OP. Epithelioid osteosarcoma of the mandible: a rare case with unusual immunoprofile. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008;105:e47-52.. Periapical lesions can be of endodontic or non-endodontic origin. Therefore, periapical radiolucency associated with root apices showed by radiographic examinations may be or not a consequence of infection of the root canal system44 - Carvalhosa AA, Araújo Estrela CR, Borges AH, Guedes OA, Estrela C. 10-year follow-up of calcifying odontogenic cyst in the periapical region of vital maxillary central incisor. J Endod. 2014;40:1695-7.,1212 - Nair PN, Sjögren U, Figdor D, Sundqvist G. Persistent periapical radiolucencies of root-filled human teeth, failed endodontic treatments, and periapical scars. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1999;87:617-27.,1313 - Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009., which may involve progressive changes in periapical structures with subsequent bone resorption1212 - Nair PN, Sjögren U, Figdor D, Sundqvist G. Persistent periapical radiolucencies of root-filled human teeth, failed endodontic treatments, and periapical scars. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1999;87:617-27.. Conventional radiographic images are frequently used to detect apical periodontitis. The diagnosis of a periapical radiolucency requires careful and correct management of information obtained from patient history, clinical examination, pulp vitality testing, and radiography analysis22 - Bregni RC, Contreras E, Hiraki KR, Vargas PA, León JE, Almeida OP. Epithelioid osteosarcoma of the mandible: a rare case with unusual immunoprofile. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008;105:e47-52.,44 - Carvalhosa AA, Araújo Estrela CR, Borges AH, Guedes OA, Estrela C. 10-year follow-up of calcifying odontogenic cyst in the periapical region of vital maxillary central incisor. J Endod. 2014;40:1695-7.,1313 - Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009.. The establishment of diagnostic procedures, such as examination of signs and symptoms, as well as complementary examinations, is indispensable to obtain differential diagnosis. Lesions of non-endodontic origin may be associated with the periapical area of the tooth33 - Bueno MR, Carvalhosa AA, Castro PH, Pereira KC, Borges FT, Estrela C. Mesenchymal chondrosarcoma mimicking apical periodontitis. J Endod. 2008;34:1415-9.,55 - Carvalhosa AA, Zandonade RM, Souza Castro PH, Araújo Estrela CR, Borges AH, Estrela C. 8-year follow-up of central giant cell lesion mimicking apical periodontitis. J Endod. 2014;40:1708-12.,88 - Faitaroni LA, Bueno MR, Carvalhosa AA, Bruehmueller Ale KA, Estrela C. Ameloblastoma suggesting large apical periodontitis. J Endod. 2008;34:216-9.,1616 - Pontes FS, Fonseca FP, Jesus AS, Garcia-Alves AC, Araújo LM, Nascimento LS, et al. Nonendodontic lesions misdiagnosed as apical periodontitis lesions: series of case reports and review of literature. J Endod. 2014;40:16-27.,1818 - Rodrigues CD, Villar-Neto MJ, Sobral AP, Silveira MM, Silva LB, Estrela C. Lymphangioma mimicking apical periodontitis. J Endod. 2011;37:91-6..
Osteosarcoma is a rare malignant neoplasm (incidence of 0.7 per million)2020 - Saito K, Unni KK. Malignant tumours of bone and cartilage. In: Barnes L, Eveson JW, Reichart P, Sidransky D. World Health Organization Classification of Tumours. Pathology and genetics of head and neck tumours. Lyon: IARC Press; 2005. of mesenchymal origin characterized by the production of immature bone1313 - Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009.. It represents 5% to 13% of total osteosarcomas66 - Chaudhary M Chaudhary SD. Osteosarcoma of jaws. J Oral Maxillofac Pathol. 2012;16:233-8.,77 - Chittaranjan B, Tejasvi MA, Babu BB, Geetha P. Intramedullary osteosarcoma of the mandible: a clinicoradiologic perspective. J Clin Imaging Sci. 2014;31:4-6.,99 - Fernandes R, Nikitakis NG, Pazoki A, Ord RA. Osteogenic sarcoma of the jaw: a 10-year experience. J Oral Maxillofac Surg. 2007;65:1286-91.,1010 - Garrington GE, Scofield HH, Cornyn J, Hooker SP. Osteosarcoma of the jaw. Analysis of 56 cases. Cancer. 1967;20:377-91.,1313 - Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009.
14 - Nthumba PM. Osteosarcoma of the jaws: a review of literature and a case report on synchronous multicentric osteosarcomas. World J Surg Oncol. 2012;10:240.-1515 - Paparella ML, Olvi LG, Brandizzi D, Keszler A, Santini-Araujo E, Cabrini RL. Osteosarcoma of the jaw: an analysis of a series of 74 cases. Histopathology. 2013;63:551-7. and occurs in the maxilla and mandible with approximately equal frequency1313 - Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009..
In the present report we describe a case of chondroblastic osteosarcoma resembling a periapical abscess in an 18-year-old male.
Case report
An 18-year-old male patient was referred to the dental clinic of the Federal University of Goiás (Goiânia, GO, Brazil) with a chief complaint of a “discomfort on the right posterior gingiva” for over a month. At physical examination, a small expansion and redness were found in the buccal and lingual cortical plates of the right mandible in the region of teeth #29, #30, and #31, but no signs of pain or inflammation were observed (Figure 1A). The overlying mucosa appeared intact.
Clinical aspect (A) showing expansion of buccal and lingual cortical plates of the right mandible in the region of teeth #29, #30, and #31, with some redness and apparently intact overlying mucosa. Periapical and panoramic radiographs (B-C) showing slight apical radiolucency in the roots of teeth #29 and #30 with loss of lamina dura and periodontal ligament space widening
Periapical and panoramic radiographs showed periapical radiolucency ranging from 4 to 5 mm in the mesial and distal roots of teeth #29 and #30, a slight rarefaction of the inter-dental alveolar bone, a clear periodontal ligament space widening, and an evident loss of lamina dura (Figure 1 B-C).
The patient reported no history of dental trauma. Neither cracks on the crowns of teeth #29 and #30, particularly on the mesial and distal marginal ridges, nor previous restorative treatments, were found. Pulp vitality testing using tetrafluoroethane spray (Endo-Ice; Hygenic Corp, Akron, OH) confirmed positive response in all teeth associated with radiolucent lesions, and therefore root canals were not treated.
Cone beam computed tomography (CBCT) images were acquired. The imaging examinations showed undefined periapical osteolytic lesion, represented by a hypodense lesion with hyperdense areas inside, and thinning of the lingual cortical plate, associated with the roots of teeth #29 and #30. Alterations in trabecular bone were also seen (Figures 2 and 3).
Cone beam computed tomography (A–B) showing a well-defined osteolytic lesion associated with the roots of teeth #29 and #30. Cross-sectional image (B) allowed observing alterations in the trabecular bone
Axial plane cone beam computed tomography showing a thinning of the buccal and lingual cortical plates (arrows).
Based on location of the lesion, its radiographic findings and the fact that periapical inflammatory lesions are the most frequent injuries in the affected region, the initial diagnosis included periapical abscess. However, given that the lesion had no relationship with pulp necrosis associated with the previous mentioned clinical and radiographic characteristics, intraosseous malignancies were considered, and an incisional biopsy was carried out. Microscopic evaluation showed a proliferation of round to spindle-shaped cells, with occasional cellular pleomorphism and variable osteoid production (Figure 4 A–B). Additionally, a focal area presented proliferation of atypical chondroblastic cells. Immunohistochemical reaction with Ki-67 marker showed evident cellular activity in the specimen (Figure 4C). Based on microscopic findings, a final diagnosis of chondroblastic osteosarcoma was confirmed.
Histopathologic examination demonstrated round to spindle-shaped cells with cellular pleomorphism (A) and osteoid production (B). A focal area presenting proliferation of atypical chondroblastic cells was observed (arrows) (hematoxylin-eosin, original magnification 100X). Immunohistochemical reaction with Ki-67 (C) marker showed evident cellular activity in the specimen
The patient returned to the dental clinic 10 days after the incisional biopsy presenting with a considerable enlargement of the region. At this time, the patient was referred to Araújo Jorge Cancer Hospital (Goiânia, GO, Brazil). The treatment consisted of hemimandibulectomy with wide surgical margins and adjuvant chemotherapy.
After surgical treatment, the patient underwent reconstruction of the right mandible with a fibular graft (Figure 5A). At the follow-up one year later, a bone scintigraphy was performed and no signs of bone metastases were seen (Figure 5B).
Panoramic radiograph (A) showing the reconstruction of the right mandible after surgical treatment. At the follow-up one year later bone scintigraphy (B) showed no signs of bone metastases
Discussion
Osteosarcoma (osteogenic sarcoma) is a primary malignant tumor of the bone in which the neoplastic cells produce osteoid or bone matrix2020 - Saito K, Unni KK. Malignant tumours of bone and cartilage. In: Barnes L, Eveson JW, Reichart P, Sidransky D. World Health Organization Classification of Tumours. Pathology and genetics of head and neck tumours. Lyon: IARC Press; 2005.. Excluding nonhematopoietic lesions, osteosarcomas are the most common primary malignant bone tumors1313 - Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009., which occur in the maxilla and mandible with approximately equal frequency1313 - Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009.,2020 - Saito K, Unni KK. Malignant tumours of bone and cartilage. In: Barnes L, Eveson JW, Reichart P, Sidransky D. World Health Organization Classification of Tumours. Pathology and genetics of head and neck tumours. Lyon: IARC Press; 2005., predominantly in adolescents and young adults, between the ages of 10 and 20 years, and is slightly more common in males2020 - Saito K, Unni KK. Malignant tumours of bone and cartilage. In: Barnes L, Eveson JW, Reichart P, Sidransky D. World Health Organization Classification of Tumours. Pathology and genetics of head and neck tumours. Lyon: IARC Press; 2005..
An increase in volume in the affected area and pain are the most common symptoms of osteosarcoma1313 - Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009., and when it occurs in the maxilla, nasal obstruction may be present1313 - Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009.,1717 - Praveena NM, Maragathavalli G. Osteosarcoma of maxilla. J Indian Acad Oral Med Radiol. 2012;24:236-8.. The etiology of osteosarcoma are still unknown, however it has been associated with preexisting conditions, including prior radiation, fibrous dysplasia, Paget’s disease, and chronic osteomyelitis1919 - Saini R, Abd Razak NH, Ab Rahman SA, Samsudin AR. Chondrosarcoma of the mandible: a case report. J Can Dent Assoc. 2007;73:175-8.,2020 - Saito K, Unni KK. Malignant tumours of bone and cartilage. In: Barnes L, Eveson JW, Reichart P, Sidransky D. World Health Organization Classification of Tumours. Pathology and genetics of head and neck tumours. Lyon: IARC Press; 2005.,2121 - Soares RC, Soares AF, Souza LB, Santos ALV, Pinto LP. Osteosarcoma of mandible initially resembling lesion of dental periapex: case report. Rev Bras Otorrinolaringol. 2005;71:242-5..
In the case reported here, clinical findings were in accordance with previous descriptions of osteosarcoma66 - Chaudhary M Chaudhary SD. Osteosarcoma of jaws. J Oral Maxillofac Pathol. 2012;16:233-8.,99 - Fernandes R, Nikitakis NG, Pazoki A, Ord RA. Osteogenic sarcoma of the jaw: a 10-year experience. J Oral Maxillofac Surg. 2007;65:1286-91.,1010 - Garrington GE, Scofield HH, Cornyn J, Hooker SP. Osteosarcoma of the jaw. Analysis of 56 cases. Cancer. 1967;20:377-91.,1313 - Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009.
14 - Nthumba PM. Osteosarcoma of the jaws: a review of literature and a case report on synchronous multicentric osteosarcomas. World J Surg Oncol. 2012;10:240.-1515 - Paparella ML, Olvi LG, Brandizzi D, Keszler A, Santini-Araujo E, Cabrini RL. Osteosarcoma of the jaw: an analysis of a series of 74 cases. Histopathology. 2013;63:551-7.,1717 - Praveena NM, Maragathavalli G. Osteosarcoma of maxilla. J Indian Acad Oral Med Radiol. 2012;24:236-8.,1919 - Saini R, Abd Razak NH, Ab Rahman SA, Samsudin AR. Chondrosarcoma of the mandible: a case report. J Can Dent Assoc. 2007;73:175-8.,2121 - Soares RC, Soares AF, Souza LB, Santos ALV, Pinto LP. Osteosarcoma of mandible initially resembling lesion of dental periapex: case report. Rev Bras Otorrinolaringol. 2005;71:242-5.,2222 - Takahama A Jr, Alves FA, Pinto CA, Carvalho AL, Kowalski LP, Lopes MA. Clinicopathological and immunohistochemical analysis of twenty-five head and neck osteosarcomas. Oral Oncol. 2003;39:521-30., since the patient was an 18-year-old man who complained of pain, the lesion was in the posterior region of the mandible, and clinical examinations showed a swelling in the affected area.
The clinical features of the lesion associated with presence of pain, swelling, and radiographic image of increased periodontal space mimicked a clinical condition of periapical abscess. Thus, based on these aspects, the initial differential diagnosis included periapical abscess. However, the positive response to pulp vitality testing suggested absence of root canal infection, which led to the recommendation of complementary examinations such as CBCT and an incisional biopsy. Due to the presence of an ill-defined radiolucency and periodontal space widening related with a vital pulp, intraosseous malignancies were considered in the differential diagnosis.
Common radiographic findings of osteosarcoma usually range from dense sclerosis to a mixed sclerotic radiolucent lesion and to a completely radiolucent process. The limits are undefined, making it difficult to determine tumor size and extension. The classic sunburst appearance is caused by osteophytic bone production on the surface of the lesion, especially in occlusal radiographs. An early radiographic change consists of a widening of the periodontal ligament space caused by tumor infiltration1313 - Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009.. Considering the difficulty to determine tumor extension using conventional radiography, in the case reported here CBCT was used to determine the degree of bone destruction caused by the tumor, as well as its location and extension. A hypodense lesion with hyperdense areas inside, thinning of the lingual cortical plate, and an undefined periapical osteolytic lesion associated with the roots of teeth #29 and #30 were found.
The macroscopic essential criterion to characterize an osteosarcoma is the direct production of osteoid by malignant mesenchymal cells1313 - Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009.. In addition to osteoid formation, tumor cells may produce chondroid material and fibrous connective tissue. Depending on the relative amounts of osteoid, cartilage, or collagen fibers, this type of tumor can be subdivided in osteoblastic, chondroblastic, and fibroblastic11 - Bennett JH, Thomas G, Evans AW, Speight PM. Osteosarcoma of the jaws: a 30-year retrospective review. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2000;90:323-32.,1313 - Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009.. Osteosarcomas of the jaws are generally better differentiated than the extragnathic ones, and they commonly exhibit chondroblastic differentiation, characterized by lobules of atypical-appearing chondrocytes in lacunae2020 - Saito K, Unni KK. Malignant tumours of bone and cartilage. In: Barnes L, Eveson JW, Reichart P, Sidransky D. World Health Organization Classification of Tumours. Pathology and genetics of head and neck tumours. Lyon: IARC Press; 2005..
In the present report, the microscopic analysis showed a proliferation of round to spindle-shaped cells, with occasional cellular pleomorphism and variable osteoid production, as well as a focal area presenting proliferation of atypical chondroblastic cells. Cellular activity was confirmed by immunohistochemical reaction with Ki-67 marker. The histopathological examination confirmed the diagnosis of chondroblastic osteosarcoma.
Takahama, et al.2222 - Takahama A Jr, Alves FA, Pinto CA, Carvalho AL, Kowalski LP, Lopes MA. Clinicopathological and immunohistochemical analysis of twenty-five head and neck osteosarcomas. Oral Oncol. 2003;39:521-30. (2003) analyzed the clinic pathological features and immunohistochemical expression of p53, MDM2, CDK4, PCNA, and Ki67 proteins in 25 head and neck osteosarcomas. The immunohistochemical analysis displayed positivity in 88% of the cases for Ki-67. Paparella, et al.1515 - Paparella ML, Olvi LG, Brandizzi D, Keszler A, Santini-Araujo E, Cabrini RL. Osteosarcoma of the jaw: an analysis of a series of 74 cases. Histopathology. 2013;63:551-7. (2013) analyzed 74 cases of osteosarcoma of the jaws and found a predominant chondroblastic pattern, which leads to the conclusion that these lesions may be associated with a worse prognosis. Bennet, et al.11 - Bennett JH, Thomas G, Evans AW, Speight PM. Osteosarcoma of the jaws: a 30-year retrospective review. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2000;90:323-32. (2001) conducted a 30-year retrospective review of osteosarcoma of the jaws and compared the clinical behavior of the tumors. Their goals were to assess how they differ from the reported characteristics of tumors of other sites and to report observations of clinical and diagnostic significance. They reported that most osteosarcomas had areas of chondroid formation in addition to neoplastic osteoid, the main complication was local recurrence, and metastasis was rare and occurred as a solitary process or in late stages of the disease. This was in contrast to lesions metastatic to the jaws, which were higher grade in appearance and had metastasized widely, early in the disease process. Primary osteosarcoma occurring in patients with a history of radiotherapy was typically more aggressive.
The recommended treatment of osteosarcoma has historically been the surgical resection of the lesion with safe margins associated with chemotherapy1111 - Lukschal LF, Barbosa RM, Alvarenga RL, Horta MC. Osteosarcoma in the maxila: case report. Rev Port Estomatol Med Dent Cir Maxilofac. 2013;54:48-52.,1313 - Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009.,2020 - Saito K, Unni KK. Malignant tumours of bone and cartilage. In: Barnes L, Eveson JW, Reichart P, Sidransky D. World Health Organization Classification of Tumours. Pathology and genetics of head and neck tumours. Lyon: IARC Press; 2005.. In the present report, the treatment consisted of a hemimandibulectomy with wide surgical margins and adjuvant chemotherapy, due to the highly malignant features of the tumor, with a worse prognosis and a high risk of local recurrence. The patient underwent reconstruction of the right mandible, and clinical and radiographic follow-up one year later confirmed tumor remission. Bone scintigraphy was conducted and showed no signs of bone metastases.
In summary, osteosarcomas could present similar features of some inflammatory periapical lesions, such as periapical abscess, since it also present pain, swelling and variable radiographic changes33 - Bueno MR, Carvalhosa AA, Castro PH, Pereira KC, Borges FT, Estrela C. Mesenchymal chondrosarcoma mimicking apical periodontitis. J Endod. 2008;34:1415-9..
Exceptional care should be paid to endodontic diagnoses based on clinical and radiographic findings. Since periapical lesions of non-endodontic origin may mimic periapical abscess and apical periodontitis, they should be considered before root canal treatment.
Conclusions
Non-endodontic diseases associated with tooth root apex, such as chondroblastic osteosarcoma, should be included in the differential diagnosis of jaw lesions that resemble periapical abscess. Periapical lesions may be misdiagnosed at their early stages if malignant tumors are not suspected.
Acknowledgments
This study was partially supported by grants from CNPq – National Council for Scientific and Technological Development (grant 457536/2014 to F.P.Y.S.) and PNPD/CAPES – Post-Doctoral National Program, Coordination of Higher Education and Graduate Training (process 02/2014 to B.S.F.S.). The authors also thank Dr. Alexandre Belotti for his technical assistance. The authors deny any conflicts of interest related to this study.
Reference
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1- Bennett JH, Thomas G, Evans AW, Speight PM. Osteosarcoma of the jaws: a 30-year retrospective review. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2000;90:323-32.
-
2- Bregni RC, Contreras E, Hiraki KR, Vargas PA, León JE, Almeida OP. Epithelioid osteosarcoma of the mandible: a rare case with unusual immunoprofile. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008;105:e47-52.
-
3- Bueno MR, Carvalhosa AA, Castro PH, Pereira KC, Borges FT, Estrela C. Mesenchymal chondrosarcoma mimicking apical periodontitis. J Endod. 2008;34:1415-9.
-
4- Carvalhosa AA, Araújo Estrela CR, Borges AH, Guedes OA, Estrela C. 10-year follow-up of calcifying odontogenic cyst in the periapical region of vital maxillary central incisor. J Endod. 2014;40:1695-7.
-
5- Carvalhosa AA, Zandonade RM, Souza Castro PH, Araújo Estrela CR, Borges AH, Estrela C. 8-year follow-up of central giant cell lesion mimicking apical periodontitis. J Endod. 2014;40:1708-12.
-
6- Chaudhary M Chaudhary SD. Osteosarcoma of jaws. J Oral Maxillofac Pathol. 2012;16:233-8.
-
7- Chittaranjan B, Tejasvi MA, Babu BB, Geetha P. Intramedullary osteosarcoma of the mandible: a clinicoradiologic perspective. J Clin Imaging Sci. 2014;31:4-6.
-
8- Faitaroni LA, Bueno MR, Carvalhosa AA, Bruehmueller Ale KA, Estrela C. Ameloblastoma suggesting large apical periodontitis. J Endod. 2008;34:216-9.
-
9- Fernandes R, Nikitakis NG, Pazoki A, Ord RA. Osteogenic sarcoma of the jaw: a 10-year experience. J Oral Maxillofac Surg. 2007;65:1286-91.
-
10- Garrington GE, Scofield HH, Cornyn J, Hooker SP. Osteosarcoma of the jaw. Analysis of 56 cases. Cancer. 1967;20:377-91.
-
11- Lukschal LF, Barbosa RM, Alvarenga RL, Horta MC. Osteosarcoma in the maxila: case report. Rev Port Estomatol Med Dent Cir Maxilofac. 2013;54:48-52.
-
12- Nair PN, Sjögren U, Figdor D, Sundqvist G. Persistent periapical radiolucencies of root-filled human teeth, failed endodontic treatments, and periapical scars. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1999;87:617-27.
-
13- Neville BW, Damm DD, Allen CM, Bouquot JE. Oral maxillofacial pathology, 3rd ed. Philadelphia: Elsevier; 2009.
-
14- Nthumba PM. Osteosarcoma of the jaws: a review of literature and a case report on synchronous multicentric osteosarcomas. World J Surg Oncol. 2012;10:240.
-
15- Paparella ML, Olvi LG, Brandizzi D, Keszler A, Santini-Araujo E, Cabrini RL. Osteosarcoma of the jaw: an analysis of a series of 74 cases. Histopathology. 2013;63:551-7.
-
16- Pontes FS, Fonseca FP, Jesus AS, Garcia-Alves AC, Araújo LM, Nascimento LS, et al. Nonendodontic lesions misdiagnosed as apical periodontitis lesions: series of case reports and review of literature. J Endod. 2014;40:16-27.
-
17- Praveena NM, Maragathavalli G. Osteosarcoma of maxilla. J Indian Acad Oral Med Radiol. 2012;24:236-8.
-
18- Rodrigues CD, Villar-Neto MJ, Sobral AP, Silveira MM, Silva LB, Estrela C. Lymphangioma mimicking apical periodontitis. J Endod. 2011;37:91-6.
-
19- Saini R, Abd Razak NH, Ab Rahman SA, Samsudin AR. Chondrosarcoma of the mandible: a case report. J Can Dent Assoc. 2007;73:175-8.
-
20- Saito K, Unni KK. Malignant tumours of bone and cartilage. In: Barnes L, Eveson JW, Reichart P, Sidransky D. World Health Organization Classification of Tumours. Pathology and genetics of head and neck tumours. Lyon: IARC Press; 2005.
-
21- Soares RC, Soares AF, Souza LB, Santos ALV, Pinto LP. Osteosarcoma of mandible initially resembling lesion of dental periapex: case report. Rev Bras Otorrinolaringol. 2005;71:242-5.
-
22- Takahama A Jr, Alves FA, Pinto CA, Carvalho AL, Kowalski LP, Lopes MA. Clinicopathological and immunohistochemical analysis of twenty-five head and neck osteosarcomas. Oral Oncol. 2003;39:521-30.
Publication Dates
-
Publication in this collection
Jul-Aug 2017
History
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Received
11 Aug 2016 -
Reviewed
26 Oct 2016 -
Accepted
4 Nov 2016