2015
DOI: 10.7860/jcdr/2015/15817.6776
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Bilateral Calcifying Cystic Odontogenic Tumour of Mandible: A Rare Case Report and Review of Literature

Abstract: Calcifying cystic odontogenic tumour (CCOT) is a relatively rare lesion of oral and maxillofacial region and forms only 2% of all odontogenic tumours. It was previously known as Calcifying odontogenic cyst and only recently has been classified as a tumour by WHO. The controversy regarding its origin can be owed to its diverse clinical and histopathological presentation and variation in reported malignant potential. It was first reported by Gorlin in 1962 and since then conundrum regarding its true nature has p… Show more

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Cited by 4 publications
(3 citation statements)
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“…Thus, as the lesion included tooth 13, extended into the amelo-cementary junction, and was located in the anterior region of the maxilla, we made a diagnosis of TOA [8]. Even though radiography is a tool for the diagnosis of COCs, it has insufficient pathognomonic characteristics to guide the final resolution of the case, which is dependent on histopathological examination [12].…”
Section: Discussionmentioning
confidence: 99%
“…Thus, as the lesion included tooth 13, extended into the amelo-cementary junction, and was located in the anterior region of the maxilla, we made a diagnosis of TOA [8]. Even though radiography is a tool for the diagnosis of COCs, it has insufficient pathognomonic characteristics to guide the final resolution of the case, which is dependent on histopathological examination [12].…”
Section: Discussionmentioning
confidence: 99%
“…It is this unique feature that also differentiates it from an ameloblastoma. However, the synchronous occurrence of COC with ameloblastomas and other odontogenic pathologies including dentigerous cysts, ameloblastic fibromas and odontomas has been reported. COCs are complex lesions and can have substantial variation in the morphology of the epithelium, with several different lesions incorporated, including other odontogenic cysts and/or tumours.…”
Section: Discussionmentioning
confidence: 99%
“…Even a case simultaneously presenting an OKC and bilateral DC was reported [24]. Other multiple DOCs, such as multiple OOCs [25,26], BCs/LPCs [27], COCs [28,29], and GOCs [30,31] are very rare and, to the best of our knowledge, are not associated with any syndrome. This retrospective study aimed (i) to evaluate the distribution of various types DOCs in patients presenting with these cysts over the last ten years in a large university hospital in the Czech Republic serving a population of approx.…”
Section: Introductionmentioning
confidence: 98%