Ameloblastomatous CCOT: A Case Report of a Rare Variant of CCOT with a Review of the Literature on Its Diverse Histopathologic Presentation
Calcifying odontogenic cyst is considered as a rare lesion and accounts for 1% of jaw cysts. It represents a heterogeneous group of lesions which exhibit a variety of clinicopathologic and behavioral features. It has been categorized as cyst and neoplasm. Even after several classification and subcla...
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doaj-bb983ba84de242cc8cc04c5daddedea12021-07-02T09:59:32ZengHindawi LimitedCase Reports in Dentistry2090-64472090-64552013-01-01201310.1155/2013/407656407656Ameloblastomatous CCOT: A Case Report of a Rare Variant of CCOT with a Review of the Literature on Its Diverse Histopathologic PresentationShailesh Menat0Shylaja MD1Kailash Attur2Kaushal Goyal3Department of Oral and Maxillofacial Surgery, Narsinhbhai Patel Dental College and Hospital, Visnagar, Gujarat 384315, IndiaDepartment of Oral Pathology and Microbiology, Narsinhbhai Patel Dental College and Hospital, Visnagar, Gujarat 384315, IndiaDepartment of Conservative and Endodontics, Narsinhbhai Patel Dental College and Hospital, Visnagar, Gujarat 384315, IndiaDepartment of Oral and Maxillofacial Surgery, Narsinhbhai Patel Dental College and Hospital, Visnagar, Gujarat 384315, IndiaCalcifying odontogenic cyst is considered as a rare lesion and accounts for 1% of jaw cysts. It represents a heterogeneous group of lesions which exhibit a variety of clinicopathologic and behavioral features. It has been categorized as cyst and neoplasm. Even after several classification and subclassification, COC remains an enigma. WHO classification 2005 has reclassified the lesion as calcifying cystic odontogenic tumor (CCOT). Ameloblastomatous COC is a rare variant which is not much described in the literature. This report describes one such case which was large multicystic, involved the coronoid and condylar process of the mandible, and treated by subhemimandibulectomy. The case was recurrence free even after 1 year of followup.http://dx.doi.org/10.1155/2013/407656 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shailesh Menat Shylaja MD Kailash Attur Kaushal Goyal |
spellingShingle |
Shailesh Menat Shylaja MD Kailash Attur Kaushal Goyal Ameloblastomatous CCOT: A Case Report of a Rare Variant of CCOT with a Review of the Literature on Its Diverse Histopathologic Presentation Case Reports in Dentistry |
author_facet |
Shailesh Menat Shylaja MD Kailash Attur Kaushal Goyal |
author_sort |
Shailesh Menat |
title |
Ameloblastomatous CCOT: A Case Report of a Rare Variant of CCOT with a Review of the Literature on Its Diverse Histopathologic Presentation |
title_short |
Ameloblastomatous CCOT: A Case Report of a Rare Variant of CCOT with a Review of the Literature on Its Diverse Histopathologic Presentation |
title_full |
Ameloblastomatous CCOT: A Case Report of a Rare Variant of CCOT with a Review of the Literature on Its Diverse Histopathologic Presentation |
title_fullStr |
Ameloblastomatous CCOT: A Case Report of a Rare Variant of CCOT with a Review of the Literature on Its Diverse Histopathologic Presentation |
title_full_unstemmed |
Ameloblastomatous CCOT: A Case Report of a Rare Variant of CCOT with a Review of the Literature on Its Diverse Histopathologic Presentation |
title_sort |
ameloblastomatous ccot: a case report of a rare variant of ccot with a review of the literature on its diverse histopathologic presentation |
publisher |
Hindawi Limited |
series |
Case Reports in Dentistry |
issn |
2090-6447 2090-6455 |
publishDate |
2013-01-01 |
description |
Calcifying odontogenic cyst is considered as a rare lesion and accounts for 1% of jaw cysts. It represents a heterogeneous group of lesions which exhibit a variety of clinicopathologic and behavioral features. It has been categorized as cyst and neoplasm. Even after several classification and subclassification, COC remains an enigma. WHO classification 2005 has reclassified the lesion as calcifying cystic odontogenic tumor (CCOT). Ameloblastomatous COC is a rare variant which is not much described in the literature. This report describes one such case which was large multicystic, involved the coronoid and condylar process of the mandible, and treated by subhemimandibulectomy. The case was recurrence free even after 1 year of followup. |
url |
http://dx.doi.org/10.1155/2013/407656 |
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