Orthokeratinized Odontogenic Cyst: A Clinicopathologic Study of 61 Cases
* Context.--Orthokeratinized odontogenic cyst (OOC) is a relatively uncommon developmental cyst comprising about 10% of cases that had been previously coded as odontogenic keratocysts. Odontogenic keratocyst was designated as keratocystic odontogenic tumor (KCOT) in the new World Health Organization...
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Veröffentlicht in: | Archives of pathology & laboratory medicine (1976) 2010-02, Vol.134 (2), p.271-275 |
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description | * Context.--Orthokeratinized odontogenic cyst (OOC) is a relatively uncommon developmental cyst comprising about 10% of cases that had been previously coded as odontogenic keratocysts. Odontogenic keratocyst was designated as keratocystic odontogenic tumor (KCOT) in the new World Health Organization classification and OOC should be distinguished from KCOT for differences in histologic features and biologic behavior. Objective.--To analyze the clinicopathologic features of 61 cases of OOC in a Chinese population. Design.--Clinicopathologic analysis was performed on 61 cases of OOC. Immunohistochemical expression of Ki-67 and p63 was evaluated in 15 OOCs and 15 typical KCOTs. Results.--The 61 patients with OOC ranged from 13 to 75 years (average, 38.93 years). The lesions developed mainly in the third and fourth decades (57.38%) with a distinct predilection for males (72.13%). Six (9.84%) lesions were found in the maxilla and 55 (90.16%) in the mandible. The most common sites were in the mandibular molar and ramus region. Of the 54 cases with radiographic record, 47 (87.04%) were unilocular and 7 (12.96%) were multilocular radiolucencies. Twenty-seven of the 54 cysts were associated with an impacted tooth. Follow-up of 42 patients revealed no recurrence during an average period of 76.8 months after surgery. Compared with KCOTs, expression level of Ki-67 and p63 was significantly lower in OOCs, suggesting a lower proliferative activity. Conclusion.--Orthokeratinized odontogenic cyst is clinicopathologically distinct from KCOT and should constitute its own clinical entity. (Arch Pathol Lab Med. 2010;134:271-275) |
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Odontogenic keratocyst was designated as keratocystic odontogenic tumor (KCOT) in the new World Health Organization classification and OOC should be distinguished from KCOT for differences in histologic features and biologic behavior. Objective.--To analyze the clinicopathologic features of 61 cases of OOC in a Chinese population. Design.--Clinicopathologic analysis was performed on 61 cases of OOC. Immunohistochemical expression of Ki-67 and p63 was evaluated in 15 OOCs and 15 typical KCOTs. Results.--The 61 patients with OOC ranged from 13 to 75 years (average, 38.93 years). The lesions developed mainly in the third and fourth decades (57.38%) with a distinct predilection for males (72.13%). Six (9.84%) lesions were found in the maxilla and 55 (90.16%) in the mandible. The most common sites were in the mandibular molar and ramus region. Of the 54 cases with radiographic record, 47 (87.04%) were unilocular and 7 (12.96%) were multilocular radiolucencies. Twenty-seven of the 54 cysts were associated with an impacted tooth. Follow-up of 42 patients revealed no recurrence during an average period of 76.8 months after surgery. Compared with KCOTs, expression level of Ki-67 and p63 was significantly lower in OOCs, suggesting a lower proliferative activity. Conclusion.--Orthokeratinized odontogenic cyst is clinicopathologically distinct from KCOT and should constitute its own clinical entity. (Arch Pathol Lab Med. 2010;134:271-275)</description><identifier>ISSN: 0003-9985</identifier><identifier>ISSN: 1543-2165</identifier><identifier>EISSN: 1543-2165</identifier><identifier>DOI: 10.5858/134.2.271</identifier><identifier>CODEN: APLMAS</identifier><language>eng</language><publisher>Northfield: College of American Pathologists</publisher><subject>Care and treatment ; Cysts ; Decades ; Development and progression ; Diagnosis ; Monoclonal antibodies ; Patient outcomes ; Software</subject><ispartof>Archives of pathology & laboratory medicine (1976), 2010-02, Vol.134 (2), p.271-275</ispartof><rights>COPYRIGHT 2010 College of American Pathologists</rights><rights>Copyright College of American Pathologists Feb 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-4c6213e961066ff9ecc968c84bb2cdaa2bc4f20afb15db9bc04e056ee150d3cd3</citedby><cites>FETCH-LOGICAL-c458t-4c6213e961066ff9ecc968c84bb2cdaa2bc4f20afb15db9bc04e056ee150d3cd3</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></links><search><creatorcontrib>Dong, Qing</creatorcontrib><creatorcontrib>Pan, Shuang</creatorcontrib><creatorcontrib>Sun, Li-Sha</creatorcontrib><creatorcontrib>Li, Tie-Jun</creatorcontrib><title>Orthokeratinized Odontogenic Cyst: A Clinicopathologic Study of 61 Cases</title><title>Archives of pathology & laboratory medicine (1976)</title><description>* Context.--Orthokeratinized odontogenic cyst (OOC) is a relatively uncommon developmental cyst comprising about 10% of cases that had been previously coded as odontogenic keratocysts. Odontogenic keratocyst was designated as keratocystic odontogenic tumor (KCOT) in the new World Health Organization classification and OOC should be distinguished from KCOT for differences in histologic features and biologic behavior. Objective.--To analyze the clinicopathologic features of 61 cases of OOC in a Chinese population. Design.--Clinicopathologic analysis was performed on 61 cases of OOC. Immunohistochemical expression of Ki-67 and p63 was evaluated in 15 OOCs and 15 typical KCOTs. Results.--The 61 patients with OOC ranged from 13 to 75 years (average, 38.93 years). The lesions developed mainly in the third and fourth decades (57.38%) with a distinct predilection for males (72.13%). Six (9.84%) lesions were found in the maxilla and 55 (90.16%) in the mandible. The most common sites were in the mandibular molar and ramus region. Of the 54 cases with radiographic record, 47 (87.04%) were unilocular and 7 (12.96%) were multilocular radiolucencies. Twenty-seven of the 54 cysts were associated with an impacted tooth. Follow-up of 42 patients revealed no recurrence during an average period of 76.8 months after surgery. Compared with KCOTs, expression level of Ki-67 and p63 was significantly lower in OOCs, suggesting a lower proliferative activity. Conclusion.--Orthokeratinized odontogenic cyst is clinicopathologically distinct from KCOT and should constitute its own clinical entity. (Arch Pathol Lab Med. 2010;134:271-275)</description><subject>Care and treatment</subject><subject>Cysts</subject><subject>Decades</subject><subject>Development and progression</subject><subject>Diagnosis</subject><subject>Monoclonal antibodies</subject><subject>Patient outcomes</subject><subject>Software</subject><issn>0003-9985</issn><issn>1543-2165</issn><issn>1543-2165</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNptkU1LAzEQhoMoWKsH_8GiIHjYmo9N3Hgri1qh0IN6Dtl8tKnbTU2yh_rrjdSDQslhyLzPJDPzAnCJ4ITWtL5DpJrgCb5HR2CEaEVKjBg9BiMIISk5r-kpOItxna8cYzQCs0VIK_9hgkyud19GFwvt--SXpneqaHYxPRTToumyqPxWZrbzy6y8pkHvCm8LhopGRhPPwYmVXTQXv3EM3p8e35pZOV88vzTTeakqWqeyUgwjYjhDkDFruVGKs1rVVdtipaXEraoshtK2iOqWtwpWBlJmDKJQE6XJGFzt390G_zmYmMTaD6HPXwqMEGccM5qh6z20lJ0Rrrc-Bak2LioxxQTi3EpVZ6o8QOXJ8zY63xvrcvofPznA56PNJm_nUMHNn4KVkV1aRd8Nyfk-_gdv96AKPsZgrNgGt5FhJxAUP76K7KvAIvtKvgGhvpGd</recordid><startdate>20100201</startdate><enddate>20100201</enddate><creator>Dong, Qing</creator><creator>Pan, Shuang</creator><creator>Sun, Li-Sha</creator><creator>Li, Tie-Jun</creator><general>College of American Pathologists</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>20100201</creationdate><title>Orthokeratinized Odontogenic Cyst: A Clinicopathologic Study of 61 Cases</title><author>Dong, Qing ; 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Odontogenic keratocyst was designated as keratocystic odontogenic tumor (KCOT) in the new World Health Organization classification and OOC should be distinguished from KCOT for differences in histologic features and biologic behavior. Objective.--To analyze the clinicopathologic features of 61 cases of OOC in a Chinese population. Design.--Clinicopathologic analysis was performed on 61 cases of OOC. Immunohistochemical expression of Ki-67 and p63 was evaluated in 15 OOCs and 15 typical KCOTs. Results.--The 61 patients with OOC ranged from 13 to 75 years (average, 38.93 years). The lesions developed mainly in the third and fourth decades (57.38%) with a distinct predilection for males (72.13%). Six (9.84%) lesions were found in the maxilla and 55 (90.16%) in the mandible. The most common sites were in the mandibular molar and ramus region. Of the 54 cases with radiographic record, 47 (87.04%) were unilocular and 7 (12.96%) were multilocular radiolucencies. Twenty-seven of the 54 cysts were associated with an impacted tooth. Follow-up of 42 patients revealed no recurrence during an average period of 76.8 months after surgery. Compared with KCOTs, expression level of Ki-67 and p63 was significantly lower in OOCs, suggesting a lower proliferative activity. Conclusion.--Orthokeratinized odontogenic cyst is clinicopathologically distinct from KCOT and should constitute its own clinical entity. (Arch Pathol Lab Med. 2010;134:271-275)</abstract><cop>Northfield</cop><pub>College of American Pathologists</pub><doi>10.5858/134.2.271</doi><tpages>5</tpages></addata></record> |
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subjects | Care and treatment Cysts Decades Development and progression Diagnosis Monoclonal antibodies Patient outcomes Software |
title | Orthokeratinized Odontogenic Cyst: A Clinicopathologic Study of 61 Cases |
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