scholarly journals Expression of PCNA, p53 and Ki-67 in dentinogenic ghost cell tumors and calcifying cystic odontogenic tumors

Author(s):  
Bianca de Fátima Borim Pulino ◽  
Carla Silva Siqueira ◽  
Carina Magalhães Esteves Duarte ◽  
Suzana Cantanhede Orsini Machado de Sousa
Keyword(s):  
2014 ◽  
Vol 117 (5) ◽  
pp. 626-633 ◽  
Author(s):  
Wagner Gomes da Silva ◽  
Teresa Cristina Ribeiro Bartholomeu dos Santos ◽  
Márcia Grillo Cabral ◽  
Rebeca Souza Azevedo ◽  
Fábio Ramôa Pires

2020 ◽  
Vol 28 (5) ◽  
pp. 526-535
Author(s):  
José Alcides Almeida de Arruda ◽  
Diego Antônio Costa Arantes ◽  
Lauren Frenzel Schuch ◽  
Carla Mosconi ◽  
Lucas Guimarães Abreu ◽  
...  

A clear cell variant of calcifying epithelial odontogenic tumor is a rare benign odontogenic neoplasm, accounting for 33 cases described in the literature. In this article, we report a challenging example of clear cell variant of calcifying epithelial odontogenic tumor of the posterior maxilla in a 45-year-old female patient showing locally aggressive growth and recurrence. Microscopically, islands of polyhedral cells containing abundant cytoplasm, well-developed intercellular bridges blended with clear cells were observed. The nuclei were frequently pleomorphic and permeated by hyaline calcified material. Immunohistochemistry revealed positivity for pan-cytokeratin (AE1/AE3), cytokeratins (CK-14 and CK-19), Bcl-2, p53, and p63. The Ki-67 proliferative index was ~10%. As odontogenic tumors are rare, when a significant clear cell component is observed, the differential diagnosis with other lesions of the jaws with similar morphology, including other odontogenic tumors with prominent clear cell component, clear cell odontogenic carcinomas, and metastatic tumors, is difficult.


2020 ◽  
Vol 10 (1) ◽  
pp. 1675-1678
Author(s):  
Pallavi Srivastava ◽  
Nidhi Anand ◽  
Nuzhat Husain

Ghost cell odontogenic carcinoma (GCOC) a rare malignant Odontogenic Carcinoma with an unpredictable behaviour presenting with local recurrences and distant metastases, to best of our knowledge about 38 cases have been reported in the past. This is an additional case of GCOC in a 25-year old female presented with a slow-growing mandibular swelling since 9 months with restricted jaw mobility. The CT scan showed an ill-defined osteodestructive lesion in the mandible. The histological examination confirms the diagnoses as a GCOC. Immunohistochemical examination was performed for Ki-67 proliferation index and p53 a predictor of progression. This case was managed by wide surgical resection of tumor and reconstruction of the defect by free fibular flap. Six months follow- up period shows no signs of recurrence. GCOC is rare Odontogenic Carcinoma with unpredictable behaviour however p53 & Ki67 proliferation index can predict the progression of tumor and help in differentiation from benign precursor lesions as early diagnosis & treatment of GCOC is necessary to prevent local recurrences & distant metastases.


2010 ◽  
Vol 5 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Márcia Gaiger de Oliveira ◽  
Isabel da Silva Lauxen ◽  
Anna Cecília Moraes Chaves ◽  
Pantelis Varvaki Rados ◽  
Manoel Sant’Ana Filho

2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Archana Sonone ◽  
V. S. Sabane ◽  
Rajeev Desai

The calcifying ghost cell odontogenic cyst (CGCOC) was first described by Gorlin et al. in 1962. Calcifying ghost cell odontogenic cyst is comparatively rare in occurrence, constituting about 0.37% to 2.1% of all odontogenic tumors. The most notable features of this pathologic entity are histopathological features which include a cystic lining demonstrating characteristic “Ghost” epithelial cells with a propensity to calcify. In addition, the CGCOC may be associated with other recognized odontogenic tumors, most commonly odontomas. There are variants of CGCOC according to clinical, histopathological, and radiological characteristics. Therefore a proper categorization of the cases is needed for better understanding of the pathogenesis of each variant. Here, we report a classical case of calcifying odontogenic cyst along with a brief review of literature.


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