Papilliferous keratoameloblastoma
Identifieur interne : 002070 ( Istex/Corpus ); précédent : 002069; suivant : 002071Papilliferous keratoameloblastoma
Auteurs : M. Altini ; H. Dev Slabbert ; T. JohnstonSource :
- Journal of Oral Pathology & Medicine [ 0904-2512 ] ; 1991-01.
English descriptors
- KwdEn :
- Altini, Ameloblastoma, Black woman, Case report, Connective tissue, Coronoid process, Cystic, Cystic follicles, Epithelium, Extensive necrosis, Final classification, Follicle, Further cases, Histologic, Individual cells, International association, Keratoameloblastoma, Large multilocular radiolucent lesion, Lesion, Mandible, Multilocular, Necrotic, Necrotic cells, Necrotic debris, Odontogenic, Oral pathologists, Oral pathology, Papilliferous, Papilliferous appearance, Papilliferous epithelium, Papilliferous keratoameloblastoma, Prominent nucleoli, Ramus, Slide seminar, Squamous, Squamous epithelium, Vast majority.
- Teeft :
- Altini, Ameloblastoma, Black woman, Case report, Connective tissue, Coronoid process, Cystic, Cystic follicles, Epithelium, Extensive necrosis, Final classification, Follicle, Further cases, Histologic, Individual cells, International association, Keratoameloblastoma, Large multilocular radiolucent lesion, Lesion, Mandible, Multilocular, Necrotic, Necrotic cells, Necrotic debris, Odontogenic, Oral pathologists, Oral pathology, Papilliferous, Papilliferous appearance, Papilliferous epithelium, Papilliferous keratoameloblastoma, Prominent nucleoli, Ramus, Slide seminar, Squamous, Squamous epithelium, Vast majority.
Abstract
A case of papilliferous keratoameloblastoma is reported which is only the second ever documented. The patient was a 76‐yr‐old black woman with a large expansile multilocular radiolucency of the body, angle and ramus of the mandible. Histologically the lesion consisted of sheets of cystic follicles filled with necrotic debris and sometimes parakeratin. The vast majority of the follicles were lined by a papilliferous epithelium consisting of large rounded cells with centrally placed nuclei. True papillary projections with cores of connective tissue were also present. The remainder of the follicles were lined by a thin parakeratinising stratified squamous epithelium. Histological features characteristic of ameloblastoma were absent. Final classification of these lesions will have to await the reporting of further cases.
Url:
DOI: 10.1111/j.1600-0714.1991.tb00887.x
Links to Exploration step
ISTEX:42C1C08AA06B73380D1E71AD39C7E914187D9AFCLe document en format XML
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Dev Slabbert</name><affiliation><mods:affiliation>Department of Oral Pathology, University of the Witwatersrand, Johannesburg, South Africa</mods:affiliation></affiliation></author><author><name sortKey="Johnston, T" sort="Johnston, T" uniqKey="Johnston T" first="T." last="Johnston">T. 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The patient was a 76‐yr‐old black woman with a large expansile multilocular radiolucency of the body, angle and ramus of the mandible. Histologically the lesion consisted of sheets of cystic follicles filled with necrotic debris and sometimes parakeratin. The vast majority of the follicles were lined by a papilliferous epithelium consisting of large rounded cells with centrally placed nuclei. True papillary projections with cores of connective tissue were also present. The remainder of the follicles were lined by a thin parakeratinising stratified squamous epithelium. Histological features characteristic of ameloblastoma were absent. 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Altini</name><affiliations><json:string>Department of Oral Pathology, University of the Witwatersrand, Johannesburg, South Africa</json:string><json:string>Correspondence address: M. Altini, Department of Oral Pathology, University of the Witwatersrand, P O WITS, 2050 South Africa.</json:string></affiliations></json:item><json:item><name>H deV Slabbert</name><affiliations><json:string>Department of Oral Pathology, University of the Witwatersrand, Johannesburg, South Africa</json:string></affiliations></json:item><json:item><name>T. Johnston</name><affiliations><json:string>Department of Maxillofacial and Oral Surgery**, University of the Witwatersrand, Johannesburg, South Africa</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>jaws, neoplasms</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>keratoameloblastoma</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>odontogenic tumor</value></json:item></subject><articleId><json:string>JOP46</json:string></articleId><arkIstex>ark:/67375/WNG-W219VRQX-6</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>caseStudy</json:string></originalGenre><abstract>A case of papilliferous keratoameloblastoma is reported which is only the second ever documented. The patient was a 76‐yr‐old black woman with a large expansile multilocular radiolucency of the body, angle and ramus of the mandible. Histologically the lesion consisted of sheets of cystic follicles filled with necrotic debris and sometimes parakeratin. The vast majority of the follicles were lined by a papilliferous epithelium consisting of large rounded cells with centrally placed nuclei. True papillary projections with cores of connective tissue were also present. The remainder of the follicles were lined by a thin parakeratinising stratified squamous epithelium. Histological features characteristic of ameloblastoma were absent. 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Altini, Department of Oral Pathology, University of the Witwatersrand, P O WITS, 2050 South Africa.</affiliation></author><author xml:id="author-0001"><persName><forename type="first">H</forename><surname>Slabbert</surname></persName><affiliation>Department of Oral Pathology, University of the Witwatersrand, Johannesburg, South Africa<address><country key="ZA"></country></address></affiliation></author><author xml:id="author-0002"><persName><forename type="first">T.</forename><surname>Johnston</surname></persName><affiliation>Department of Maxillofacial and Oral Surgery**, University of the Witwatersrand, Johannesburg, South Africa<address><country key="ZA"></country></address></affiliation></author><idno type="istex">42C1C08AA06B73380D1E71AD39C7E914187D9AFC</idno><idno type="ark">ark:/67375/WNG-W219VRQX-6</idno><idno type="DOI">10.1111/j.1600-0714.1991.tb00887.x</idno><idno type="unit">JOP46</idno><idno type="toTypesetVersion">file:JOP.JOP46.pdf</idno></analytic><monogr><title level="j" type="main">Journal of Oral Pathology & Medicine</title><title level="j" type="alt">JOURNAL ORAL PATHOLOGY MEDICINE</title><idno type="pISSN">0904-2512</idno><idno type="eISSN">1600-0714</idno><idno type="book-DOI">10.1111/(ISSN)1600-0714</idno><idno type="book-part-DOI">10.1111/jop.1991.20.issue-1</idno><idno type="product">JOP</idno><idno type="publisherDivision">ST</idno><imprint><biblScope unit="vol">20</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="46">46</biblScope><biblScope unit="page" to="48">48</biblScope><biblScope unit="page-count">3</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="1991-01"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract xml:lang="en" style="main"><p>A case of papilliferous keratoameloblastoma is reported which is only the second ever documented. 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Final classification of these lesions will have to await the reporting of further cases.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Papilliferous keratoameloblastoma</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Papilliferous keratoameloblastoma</title></titleInfo><name type="personal"><namePart type="given">M.</namePart><namePart type="family">Altini</namePart><affiliation>Department of Oral Pathology, University of the Witwatersrand, Johannesburg, South Africa</affiliation><affiliation>Correspondence address: M. Altini, Department of Oral Pathology, University of the Witwatersrand, P O WITS, 2050 South Africa.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">H</namePart><namePart type="family">deV Slabbert</namePart><affiliation>Department of Oral Pathology, University of the Witwatersrand, Johannesburg, South Africa</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T.</namePart><namePart type="family">Johnston</namePart><affiliation>Department of Maxillofacial and Oral Surgery**, University of the Witwatersrand, Johannesburg, South Africa</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="case-report" displayLabel="caseStudy" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-29919SZJ-6">case-report</genre><originInfo><publisher>Blackwell Publishing Ltd</publisher><place><placeTerm type="text">Oxford, UK</placeTerm></place><dateIssued encoding="w3cdtf">1991-01</dateIssued><edition>Accepted for publication August 7, 1990.</edition><copyrightDate encoding="w3cdtf">1991</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="references">3</extent><extent unit="linksCrossRef">4</extent></physicalDescription><abstract lang="en">A case of papilliferous keratoameloblastoma is reported which is only the second ever documented. The patient was a 76‐yr‐old black woman with a large expansile multilocular radiolucency of the body, angle and ramus of the mandible. Histologically the lesion consisted of sheets of cystic follicles filled with necrotic debris and sometimes parakeratin. The vast majority of the follicles were lined by a papilliferous epithelium consisting of large rounded cells with centrally placed nuclei. True papillary projections with cores of connective tissue were also present. The remainder of the follicles were lined by a thin parakeratinising stratified squamous epithelium. Histological features characteristic of ameloblastoma were absent. Final classification of these lesions will have to await the reporting of further cases.</abstract><subject lang="en"><genre>keywords</genre><topic>jaws, neoplasms</topic><topic>keratoameloblastoma</topic><topic>odontogenic tumor</topic></subject><relatedItem type="host"><titleInfo><title>Journal of Oral Pathology & Medicine</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><identifier type="ISSN">0904-2512</identifier><identifier type="eISSN">1600-0714</identifier><identifier type="DOI">10.1111/(ISSN)1600-0714</identifier><identifier type="PublisherID">JOP</identifier><part><date>1991</date><detail type="volume"><caption>vol.</caption><number>20</number></detail><detail type="issue"><caption>no.</caption><number>1</number></detail><extent unit="pages"><start>46</start><end>48</end><total>3</total></extent></part></relatedItem><identifier type="istex">42C1C08AA06B73380D1E71AD39C7E914187D9AFC</identifier><identifier type="ark">ark:/67375/WNG-W219VRQX-6</identifier><identifier type="DOI">10.1111/j.1600-0714.1991.tb00887.x</identifier><identifier type="ArticleID">JOP46</identifier><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-L0C46X92-X">wiley</recordContentSource><recordOrigin>Blackwell Publishing Ltd</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/document/42C1C08AA06B73380D1E71AD39C7E914187D9AFC/metadata/json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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