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Dentinogenic ghost cell tumor: A case report
BACKGROUND: Dentinogenic ghost cell tumor (DGCT) is an uncommon locally invasive odontogenic neoplasm. It is considered to be a solid variant of calcifying odontogenic cyst (COC). This tumor makes up for only 2%-14% of all COCs and less than 0.5% of all odontogenic tumors which owes to its rarity. T...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6506423/ https://www.ncbi.nlm.nih.gov/pubmed/31114751 http://dx.doi.org/10.5306/wjco.v10.i4.192 |
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author | Patankar, Sangeeta R Khetan, Palak Choudhari, Sheetal K Suryavanshi, Harshal |
author_facet | Patankar, Sangeeta R Khetan, Palak Choudhari, Sheetal K Suryavanshi, Harshal |
author_sort | Patankar, Sangeeta R |
collection | PubMed |
description | BACKGROUND: Dentinogenic ghost cell tumor (DGCT) is an uncommon locally invasive odontogenic neoplasm. It is considered to be a solid variant of calcifying odontogenic cyst (COC). This tumor makes up for only 2%-14% of all COCs and less than 0.5% of all odontogenic tumors which owes to its rarity. The purpose of this paper was to describe a case of DGCT and the treatment adopted in our case, and to provide a review of this case in the indexed literature. CASE SUMMARY: In this article, we discussed a case of 18 year old male who reported with a chief complaint of a recurrent swelling and dull aching pain in upper left back region of the jaw. Computed tomography scan was carried out which revealed hypodense lesion with a few hyperdense flecks within it suggesting the presence of calcification. On incisional biopsy, diagnosis of COC was given. After segmental resection of the lesion, histopathogically odontogenic epithelium was noted along with calcifications, ghost cells and dentinoid material. Special staining was done with van Gieson and it showed pink areas of dentinoid material and yellow colour represented ghost cells. Hence, amalgamation of careful clinical examination, use of advanced radiographic imaging and detailed histopathological examination confirmed the diagnosis of DGCT. The patient was followed up for one year and there was no recurrence of the lesion or signs of any residual tumor. CONCLUSION: Radical treatment should be carried out along with mandatory long-term follow up in order to avoid recurrence in aggressive lesions. |
format | Online Article Text |
id | pubmed-6506423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-65064232019-05-21 Dentinogenic ghost cell tumor: A case report Patankar, Sangeeta R Khetan, Palak Choudhari, Sheetal K Suryavanshi, Harshal World J Clin Oncol Case Report BACKGROUND: Dentinogenic ghost cell tumor (DGCT) is an uncommon locally invasive odontogenic neoplasm. It is considered to be a solid variant of calcifying odontogenic cyst (COC). This tumor makes up for only 2%-14% of all COCs and less than 0.5% of all odontogenic tumors which owes to its rarity. The purpose of this paper was to describe a case of DGCT and the treatment adopted in our case, and to provide a review of this case in the indexed literature. CASE SUMMARY: In this article, we discussed a case of 18 year old male who reported with a chief complaint of a recurrent swelling and dull aching pain in upper left back region of the jaw. Computed tomography scan was carried out which revealed hypodense lesion with a few hyperdense flecks within it suggesting the presence of calcification. On incisional biopsy, diagnosis of COC was given. After segmental resection of the lesion, histopathogically odontogenic epithelium was noted along with calcifications, ghost cells and dentinoid material. Special staining was done with van Gieson and it showed pink areas of dentinoid material and yellow colour represented ghost cells. Hence, amalgamation of careful clinical examination, use of advanced radiographic imaging and detailed histopathological examination confirmed the diagnosis of DGCT. The patient was followed up for one year and there was no recurrence of the lesion or signs of any residual tumor. CONCLUSION: Radical treatment should be carried out along with mandatory long-term follow up in order to avoid recurrence in aggressive lesions. Baishideng Publishing Group Inc 2019-04-24 2019-04-24 /pmc/articles/PMC6506423/ /pubmed/31114751 http://dx.doi.org/10.5306/wjco.v10.i4.192 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Patankar, Sangeeta R Khetan, Palak Choudhari, Sheetal K Suryavanshi, Harshal Dentinogenic ghost cell tumor: A case report |
title | Dentinogenic ghost cell tumor: A case report |
title_full | Dentinogenic ghost cell tumor: A case report |
title_fullStr | Dentinogenic ghost cell tumor: A case report |
title_full_unstemmed | Dentinogenic ghost cell tumor: A case report |
title_short | Dentinogenic ghost cell tumor: A case report |
title_sort | dentinogenic ghost cell tumor: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6506423/ https://www.ncbi.nlm.nih.gov/pubmed/31114751 http://dx.doi.org/10.5306/wjco.v10.i4.192 |
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