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Prognostic factors for keratocystic odontogenic tumor (odontogenic keratocyst): analysis of clinico-pathologic and immunohistochemical findings in cysts treated by enucleation
Background: The purpose of this study was to determine prognostic factors for the recurrence of keratocystic odontogenic tumors (KCOTs) following simple enucleation by examining clinico‐pathologic and immunohistochemical findings. Methods: Following enucleation, the frequency of recurrence among 3...
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Published in: | Journal of oral pathology & medicine 2009-04, Vol.38 (4), p.386-392 |
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creator | Kuroyanagi, Norio Sakuma, Hidenori Miyabe, Satoru Machida, Junichiro Kaetsu, Atsuo Yokoi, Motoo Maeda, Hatsuhiko Warnakulasuriya, Saman Nagao, Toru Shimozato, Kazuo |
description | Background: The purpose of this study was to determine prognostic factors for the recurrence of keratocystic odontogenic tumors (KCOTs) following simple enucleation by examining clinico‐pathologic and immunohistochemical findings.
Methods: Following enucleation, the frequency of recurrence among 32 subjects diagnosed with KCOT was analyzed for tumor site, radiographic and histologic features, and immunopositivity for Ki‐67 and p53.
Results: Keratocystic odontogenic tumors in four out of 32 subjects (12.5%) recurred during the follow‐up period (median: 33 months, range: 7–114 months). Three out of four subjects (75.0%) among recurrent group showed high expression of Ki‐67 (LI >10%) in basal layer and four (4/28; 14.3%) among non‐recurrence group (P = 0.025). Expression of p53 among non‐recurrent group was observed in 11 subjects (11/28; 39.3%), and in three subjects (3/4; 75.0%) among the recurrent group (P = 0.295). Hazard risk for the recurrence of KCOT was 4.02 (95% CI 1.42–18.14) for high Ki‐67 expression in the basal layer by the Cox proportional hazard model (P = 0.009). In our study, none of the other clinico‐pathologic variables were associated with the recurrence of KCOT.
Conclusion: The results suggested that the evaluation of Ki‐67 expression in KCOT at the time of pathological diagnosis might be helpful for consideration of appropriate adjunctive surgical procedures to avoid a recurrence and may serve as a prognostic marker. |
doi_str_mv | 10.1111/j.1600-0714.2008.00729.x |
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Methods: Following enucleation, the frequency of recurrence among 32 subjects diagnosed with KCOT was analyzed for tumor site, radiographic and histologic features, and immunopositivity for Ki‐67 and p53.
Results: Keratocystic odontogenic tumors in four out of 32 subjects (12.5%) recurred during the follow‐up period (median: 33 months, range: 7–114 months). Three out of four subjects (75.0%) among recurrent group showed high expression of Ki‐67 (LI >10%) in basal layer and four (4/28; 14.3%) among non‐recurrence group (P = 0.025). Expression of p53 among non‐recurrent group was observed in 11 subjects (11/28; 39.3%), and in three subjects (3/4; 75.0%) among the recurrent group (P = 0.295). Hazard risk for the recurrence of KCOT was 4.02 (95% CI 1.42–18.14) for high Ki‐67 expression in the basal layer by the Cox proportional hazard model (P = 0.009). In our study, none of the other clinico‐pathologic variables were associated with the recurrence of KCOT.
Conclusion: The results suggested that the evaluation of Ki‐67 expression in KCOT at the time of pathological diagnosis might be helpful for consideration of appropriate adjunctive surgical procedures to avoid a recurrence and may serve as a prognostic marker.</description><identifier>ISSN: 0904-2512</identifier><identifier>EISSN: 1600-0714</identifier><identifier>DOI: 10.1111/j.1600-0714.2008.00729.x</identifier><identifier>PMID: 19141056</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; Aged ; Biological and medical sciences ; Dentistry ; Female ; Humans ; Immunohistochemistry ; Keratins ; keratocystic odontogenic tumor ; Ki-67 ; Ki-67 Antigen - biosynthesis ; Male ; Medical sciences ; Middle Aged ; Odontogenic Cysts - chemistry ; Odontogenic Cysts - metabolism ; Odontogenic Cysts - pathology ; Odontogenic Cysts - surgery ; odontogenic keratocyst ; Otorhinolaryngology. Stomatology ; p53 ; Prognosis ; prognostic markers ; Recurrence ; Tumor Suppressor Protein p53 - biosynthesis ; Young Adult</subject><ispartof>Journal of oral pathology & medicine, 2009-04, Vol.38 (4), p.386-392</ispartof><rights>2009 The Authors. Journal compilation © 2009 Blackwell Munksgaard</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5319-9c1efb168e0bb4388f8156ac8bfa1c9267bdbaea3b928630944c8bc6162e05af3</citedby><cites>FETCH-LOGICAL-c5319-9c1efb168e0bb4388f8156ac8bfa1c9267bdbaea3b928630944c8bc6162e05af3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21271034$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19141056$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kuroyanagi, Norio</creatorcontrib><creatorcontrib>Sakuma, Hidenori</creatorcontrib><creatorcontrib>Miyabe, Satoru</creatorcontrib><creatorcontrib>Machida, Junichiro</creatorcontrib><creatorcontrib>Kaetsu, Atsuo</creatorcontrib><creatorcontrib>Yokoi, Motoo</creatorcontrib><creatorcontrib>Maeda, Hatsuhiko</creatorcontrib><creatorcontrib>Warnakulasuriya, Saman</creatorcontrib><creatorcontrib>Nagao, Toru</creatorcontrib><creatorcontrib>Shimozato, Kazuo</creatorcontrib><title>Prognostic factors for keratocystic odontogenic tumor (odontogenic keratocyst): analysis of clinico-pathologic and immunohistochemical findings in cysts treated by enucleation</title><title>Journal of oral pathology & medicine</title><addtitle>J Oral Pathol Med</addtitle><description>Background: The purpose of this study was to determine prognostic factors for the recurrence of keratocystic odontogenic tumors (KCOTs) following simple enucleation by examining clinico‐pathologic and immunohistochemical findings.
Methods: Following enucleation, the frequency of recurrence among 32 subjects diagnosed with KCOT was analyzed for tumor site, radiographic and histologic features, and immunopositivity for Ki‐67 and p53.
Results: Keratocystic odontogenic tumors in four out of 32 subjects (12.5%) recurred during the follow‐up period (median: 33 months, range: 7–114 months). Three out of four subjects (75.0%) among recurrent group showed high expression of Ki‐67 (LI >10%) in basal layer and four (4/28; 14.3%) among non‐recurrence group (P = 0.025). Expression of p53 among non‐recurrent group was observed in 11 subjects (11/28; 39.3%), and in three subjects (3/4; 75.0%) among the recurrent group (P = 0.295). Hazard risk for the recurrence of KCOT was 4.02 (95% CI 1.42–18.14) for high Ki‐67 expression in the basal layer by the Cox proportional hazard model (P = 0.009). In our study, none of the other clinico‐pathologic variables were associated with the recurrence of KCOT.
Conclusion: The results suggested that the evaluation of Ki‐67 expression in KCOT at the time of pathological diagnosis might be helpful for consideration of appropriate adjunctive surgical procedures to avoid a recurrence and may serve as a prognostic marker.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Dentistry</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Keratins</subject><subject>keratocystic odontogenic tumor</subject><subject>Ki-67</subject><subject>Ki-67 Antigen - biosynthesis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Odontogenic Cysts - chemistry</subject><subject>Odontogenic Cysts - metabolism</subject><subject>Odontogenic Cysts - pathology</subject><subject>Odontogenic Cysts - surgery</subject><subject>odontogenic keratocyst</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>p53</subject><subject>Prognosis</subject><subject>prognostic markers</subject><subject>Recurrence</subject><subject>Tumor Suppressor Protein p53 - biosynthesis</subject><subject>Young Adult</subject><issn>0904-2512</issn><issn>1600-0714</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqNkcuO0zAUhi0EYsrAKyBvQLBI8DUXxAYVGEAVUyEQS8tx7NadxC52Ipqn4hVxplWHHXjjy__9x0fnBwBilOO0Xu1yXCCUoRKznCBU5QiVpM4P98DiLNwHC1QjlhGOyQV4FOMOIVxShh-CC1xjhhEvFuD3OviN83GwChqpBh8iND7AGx3k4NV0K_jWu8FvtEvnYeyT_OLvpzv25WsoneymaCP0BqrOJt1nezlsfec3iZWuhbbvR-e3NibTVvdWyQ4a61rrNhFaB-dKEQ5By0G3sJmgdqPq0s169xg8MLKL-slpvwTfP7z_tvyYra6vPi3frjLFKa6zWmFtGlxUGjUNo1VlKswLqarGSKxqUpRN20gtaVOTqqCoZixpqsAF0YhLQy_B82PdffA_Rx0H0duodNdJp_0YRVFixCgh_wQJ4qzilCewOoIq-BiDNmIfbC_DJDASc6piJ-bwxByemFMVt6mKQ7I-Pf0xNr1u74ynGBPw7ATImKZpgnTKxjNHMEntUpa4N0ful-309N8NiM_X63RI9uxoT9Hpw9kuw02aBy25-PHlSrxbrr7yCq3Fmv4BcYbR_g</recordid><startdate>200904</startdate><enddate>200904</enddate><creator>Kuroyanagi, Norio</creator><creator>Sakuma, Hidenori</creator><creator>Miyabe, Satoru</creator><creator>Machida, Junichiro</creator><creator>Kaetsu, Atsuo</creator><creator>Yokoi, Motoo</creator><creator>Maeda, Hatsuhiko</creator><creator>Warnakulasuriya, Saman</creator><creator>Nagao, Toru</creator><creator>Shimozato, Kazuo</creator><general>Blackwell Publishing Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7X8</scope></search><sort><creationdate>200904</creationdate><title>Prognostic factors for keratocystic odontogenic tumor (odontogenic keratocyst): analysis of clinico-pathologic and immunohistochemical findings in cysts treated by enucleation</title><author>Kuroyanagi, Norio ; Sakuma, Hidenori ; Miyabe, Satoru ; Machida, Junichiro ; Kaetsu, Atsuo ; Yokoi, Motoo ; Maeda, Hatsuhiko ; Warnakulasuriya, Saman ; Nagao, Toru ; Shimozato, Kazuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5319-9c1efb168e0bb4388f8156ac8bfa1c9267bdbaea3b928630944c8bc6162e05af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Dentistry</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Keratins</topic><topic>keratocystic odontogenic tumor</topic><topic>Ki-67</topic><topic>Ki-67 Antigen - biosynthesis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Odontogenic Cysts - chemistry</topic><topic>Odontogenic Cysts - metabolism</topic><topic>Odontogenic Cysts - pathology</topic><topic>Odontogenic Cysts - surgery</topic><topic>odontogenic keratocyst</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>p53</topic><topic>Prognosis</topic><topic>prognostic markers</topic><topic>Recurrence</topic><topic>Tumor Suppressor Protein p53 - biosynthesis</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kuroyanagi, Norio</creatorcontrib><creatorcontrib>Sakuma, Hidenori</creatorcontrib><creatorcontrib>Miyabe, Satoru</creatorcontrib><creatorcontrib>Machida, Junichiro</creatorcontrib><creatorcontrib>Kaetsu, Atsuo</creatorcontrib><creatorcontrib>Yokoi, Motoo</creatorcontrib><creatorcontrib>Maeda, Hatsuhiko</creatorcontrib><creatorcontrib>Warnakulasuriya, Saman</creatorcontrib><creatorcontrib>Nagao, Toru</creatorcontrib><creatorcontrib>Shimozato, Kazuo</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of oral pathology & medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kuroyanagi, Norio</au><au>Sakuma, Hidenori</au><au>Miyabe, Satoru</au><au>Machida, Junichiro</au><au>Kaetsu, Atsuo</au><au>Yokoi, Motoo</au><au>Maeda, Hatsuhiko</au><au>Warnakulasuriya, Saman</au><au>Nagao, Toru</au><au>Shimozato, Kazuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prognostic factors for keratocystic odontogenic tumor (odontogenic keratocyst): analysis of clinico-pathologic and immunohistochemical findings in cysts treated by enucleation</atitle><jtitle>Journal of oral pathology & medicine</jtitle><addtitle>J Oral Pathol Med</addtitle><date>2009-04</date><risdate>2009</risdate><volume>38</volume><issue>4</issue><spage>386</spage><epage>392</epage><pages>386-392</pages><issn>0904-2512</issn><eissn>1600-0714</eissn><abstract>Background: The purpose of this study was to determine prognostic factors for the recurrence of keratocystic odontogenic tumors (KCOTs) following simple enucleation by examining clinico‐pathologic and immunohistochemical findings.
Methods: Following enucleation, the frequency of recurrence among 32 subjects diagnosed with KCOT was analyzed for tumor site, radiographic and histologic features, and immunopositivity for Ki‐67 and p53.
Results: Keratocystic odontogenic tumors in four out of 32 subjects (12.5%) recurred during the follow‐up period (median: 33 months, range: 7–114 months). Three out of four subjects (75.0%) among recurrent group showed high expression of Ki‐67 (LI >10%) in basal layer and four (4/28; 14.3%) among non‐recurrence group (P = 0.025). Expression of p53 among non‐recurrent group was observed in 11 subjects (11/28; 39.3%), and in three subjects (3/4; 75.0%) among the recurrent group (P = 0.295). Hazard risk for the recurrence of KCOT was 4.02 (95% CI 1.42–18.14) for high Ki‐67 expression in the basal layer by the Cox proportional hazard model (P = 0.009). In our study, none of the other clinico‐pathologic variables were associated with the recurrence of KCOT.
Conclusion: The results suggested that the evaluation of Ki‐67 expression in KCOT at the time of pathological diagnosis might be helpful for consideration of appropriate adjunctive surgical procedures to avoid a recurrence and may serve as a prognostic marker.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>19141056</pmid><doi>10.1111/j.1600-0714.2008.00729.x</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Adult Aged Biological and medical sciences Dentistry Female Humans Immunohistochemistry Keratins keratocystic odontogenic tumor Ki-67 Ki-67 Antigen - biosynthesis Male Medical sciences Middle Aged Odontogenic Cysts - chemistry Odontogenic Cysts - metabolism Odontogenic Cysts - pathology Odontogenic Cysts - surgery odontogenic keratocyst Otorhinolaryngology. Stomatology p53 Prognosis prognostic markers Recurrence Tumor Suppressor Protein p53 - biosynthesis Young Adult |
title | Prognostic factors for keratocystic odontogenic tumor (odontogenic keratocyst): analysis of clinico-pathologic and immunohistochemical findings in cysts treated by enucleation |
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