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Management of an extensive odontogenic keratocyst: A rare case report with 10-year follow-up
INTRODUCTION: The odontogenic keratocyst (OKC), previously known as keratocystic odontogenic tumor has been the most disputable pathologies of the maxillofacial region. Patients with OKC are often asymptomatic but may present with pain, swelling, or discharge. Despite the aggressive nature, previous...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940056/ https://www.ncbi.nlm.nih.gov/pubmed/31860950 http://dx.doi.org/10.1097/MD.0000000000017987 |
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author | Khan, Abdul Ahad Qahtani, Saad Al Dawasaz, Ali Azhar Saquib, Shahabe A. Asif, Shaik Mohammed Ishfaq, Mohammad Kota, Mohammad Zahir Ibrahim, Mohammed |
author_facet | Khan, Abdul Ahad Qahtani, Saad Al Dawasaz, Ali Azhar Saquib, Shahabe A. Asif, Shaik Mohammed Ishfaq, Mohammad Kota, Mohammad Zahir Ibrahim, Mohammed |
author_sort | Khan, Abdul Ahad |
collection | PubMed |
description | INTRODUCTION: The odontogenic keratocyst (OKC), previously known as keratocystic odontogenic tumor has been the most disputable pathologies of the maxillofacial region. Patients with OKC are often asymptomatic but may present with pain, swelling, or discharge. Despite the aggressive nature, previous literature as early as 1970s reported the fact that parakeratinized OKC can be treated by means of marsupialization alone. PATIENTS CONCERNS: The patient had reported with a complaint of pain and swelling in relation with a tooth in mandibular right quadrant. DIAGNOSIS: This case report discusses features of a rare, extensive, panmandibular OKC that is only second of its kind mentioned in the literature. INTERVENTION: As a usual treatment protocol, marsupialization was attempted first. Immunohistochemical analysis revealed reduced expression of Ki-67 and B cell lymphoma 2 (bcl-2) markers after marsupialization from 2 separate sites. However, due to incomplete resolution in the lower right anterior region, an aggressive approach was taken by curetting it out surgically along with associated teeth and cortical plate followed by application of Carnoy's solution. OUTCOME: Postsurgery uneventful healing of the lesion was noted on regular follow-up visits with complete resolution at 40 months. The case has been followed for 10 years with no sign of relapse and reoccurrence. CONCLUSIONS: Based on the expression of markers it can thus be concluded that Ki-67 and bcl-2 are site specific and bear strong relationship with the recurrence of OKCs. |
format | Online Article Text |
id | pubmed-6940056 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-69400562020-01-31 Management of an extensive odontogenic keratocyst: A rare case report with 10-year follow-up Khan, Abdul Ahad Qahtani, Saad Al Dawasaz, Ali Azhar Saquib, Shahabe A. Asif, Shaik Mohammed Ishfaq, Mohammad Kota, Mohammad Zahir Ibrahim, Mohammed Medicine (Baltimore) 5900 INTRODUCTION: The odontogenic keratocyst (OKC), previously known as keratocystic odontogenic tumor has been the most disputable pathologies of the maxillofacial region. Patients with OKC are often asymptomatic but may present with pain, swelling, or discharge. Despite the aggressive nature, previous literature as early as 1970s reported the fact that parakeratinized OKC can be treated by means of marsupialization alone. PATIENTS CONCERNS: The patient had reported with a complaint of pain and swelling in relation with a tooth in mandibular right quadrant. DIAGNOSIS: This case report discusses features of a rare, extensive, panmandibular OKC that is only second of its kind mentioned in the literature. INTERVENTION: As a usual treatment protocol, marsupialization was attempted first. Immunohistochemical analysis revealed reduced expression of Ki-67 and B cell lymphoma 2 (bcl-2) markers after marsupialization from 2 separate sites. However, due to incomplete resolution in the lower right anterior region, an aggressive approach was taken by curetting it out surgically along with associated teeth and cortical plate followed by application of Carnoy's solution. OUTCOME: Postsurgery uneventful healing of the lesion was noted on regular follow-up visits with complete resolution at 40 months. The case has been followed for 10 years with no sign of relapse and reoccurrence. CONCLUSIONS: Based on the expression of markers it can thus be concluded that Ki-67 and bcl-2 are site specific and bear strong relationship with the recurrence of OKCs. Wolters Kluwer Health 2019-12-20 /pmc/articles/PMC6940056/ /pubmed/31860950 http://dx.doi.org/10.1097/MD.0000000000017987 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 5900 Khan, Abdul Ahad Qahtani, Saad Al Dawasaz, Ali Azhar Saquib, Shahabe A. Asif, Shaik Mohammed Ishfaq, Mohammad Kota, Mohammad Zahir Ibrahim, Mohammed Management of an extensive odontogenic keratocyst: A rare case report with 10-year follow-up |
title | Management of an extensive odontogenic keratocyst: A rare case report with 10-year follow-up |
title_full | Management of an extensive odontogenic keratocyst: A rare case report with 10-year follow-up |
title_fullStr | Management of an extensive odontogenic keratocyst: A rare case report with 10-year follow-up |
title_full_unstemmed | Management of an extensive odontogenic keratocyst: A rare case report with 10-year follow-up |
title_short | Management of an extensive odontogenic keratocyst: A rare case report with 10-year follow-up |
title_sort | management of an extensive odontogenic keratocyst: a rare case report with 10-year follow-up |
topic | 5900 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940056/ https://www.ncbi.nlm.nih.gov/pubmed/31860950 http://dx.doi.org/10.1097/MD.0000000000017987 |
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