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Solitary fibrous tumour of the oral cavity: clinicopathological and immunohistochemical characterization of three cases
: Solitary fibrous tumour (SFT) is an uncommon mesenchymal neoplasm rarely located in the oral cavity. To characterize further oral SFT, we describe three new cases. Each tumour originated in the buccal mucosa of a middle‐aged/elderly patient. Histological examination showed well‐circumscribed tumou...
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Published in: | Journal of oral pathology & medicine 2000-04, Vol.29 (4), p.186-192 |
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container_title | Journal of oral pathology & medicine |
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creator | Lukinmaa, Pirjo‐Liisa Hietanen, Jarkko Warfvinge, Gunnar Sane, Juha Tuominen, Susanne Henriksson, Vincent Larsson, Åke |
description | : Solitary fibrous tumour (SFT) is an uncommon mesenchymal neoplasm rarely located in the oral cavity. To characterize further oral SFT, we describe three new cases. Each tumour originated in the buccal mucosa of a middle‐aged/elderly patient. Histological examination showed well‐circumscribed tumours with densely cellular areas alternating with hypocellular areas in a variedly collagenous, vascular stroma. Mast cells were abundant. The spindle‐shaped, neoplastic cells immunostained strongly for CD34 antigen and vimentin and weakly for bcl‐2, but not for epithelial cell markers, α‐smooth muscle actin, or neurofilament or S‐100 proteins. Compatible with the virtual absence of mitoses and of marked nuclear atypia, the overall frequency of proliferating cells expressing Ki‐67 was low. The expression of CD34 was useful in the differential diagnosis. The consistent location in the cheek and expansion of one tumour after local trauma does not preclude a traumatic element in the development of oral SFT. |
doi_str_mv | 10.1034/j.1600-0714.2000.290407.x |
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To characterize further oral SFT, we describe three new cases. Each tumour originated in the buccal mucosa of a middle‐aged/elderly patient. Histological examination showed well‐circumscribed tumours with densely cellular areas alternating with hypocellular areas in a variedly collagenous, vascular stroma. Mast cells were abundant. The spindle‐shaped, neoplastic cells immunostained strongly for CD34 antigen and vimentin and weakly for bcl‐2, but not for epithelial cell markers, α‐smooth muscle actin, or neurofilament or S‐100 proteins. Compatible with the virtual absence of mitoses and of marked nuclear atypia, the overall frequency of proliferating cells expressing Ki‐67 was low. The expression of CD34 was useful in the differential diagnosis. The consistent location in the cheek and expansion of one tumour after local trauma does not preclude a traumatic element in the development of oral SFT.</description><identifier>ISSN: 0904-2512</identifier><identifier>EISSN: 1600-0714</identifier><identifier>DOI: 10.1034/j.1600-0714.2000.290407.x</identifier><identifier>PMID: 10766397</identifier><language>eng</language><publisher>Copenhagen: Munksgaard International Publishers</publisher><subject>Aged ; Antigens, CD34 - analysis ; bcl‐2 ; Biological and medical sciences ; Blood Vessels - pathology ; CD34 ; Cell Nucleus - ultrastructure ; Collagen ; Dentistry ; Diagnosis, Differential ; Female ; histology ; Humans ; Immunohistochemistry ; Ki-67 Antigen - analysis ; Male ; Mast Cells - pathology ; Medical sciences ; Middle Aged ; Mitosis ; Mouth Mucosa - pathology ; Mouth Neoplasms - pathology ; Neoplasms, Fibrous Tissue - pathology ; oral cavity ; Otorhinolaryngology. Stomatology ; Proto-Oncogene Proteins c-bcl-2 - analysis ; solitary fibrous tumour (SFT) ; Tumors ; Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology ; vimentin ; Vimentin - analysis</subject><ispartof>Journal of oral pathology & medicine, 2000-04, Vol.29 (4), p.186-192</ispartof><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3997-96f4d3de5ef8b1f67514357bbf8a7940d5dbbefbe92db6237c66d8e85f1b05ed3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1319624$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10766397$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lukinmaa, Pirjo‐Liisa</creatorcontrib><creatorcontrib>Hietanen, Jarkko</creatorcontrib><creatorcontrib>Warfvinge, Gunnar</creatorcontrib><creatorcontrib>Sane, Juha</creatorcontrib><creatorcontrib>Tuominen, Susanne</creatorcontrib><creatorcontrib>Henriksson, Vincent</creatorcontrib><creatorcontrib>Larsson, Åke</creatorcontrib><title>Solitary fibrous tumour of the oral cavity: clinicopathological and immunohistochemical characterization of three cases</title><title>Journal of oral pathology & medicine</title><addtitle>J Oral Pathol Med</addtitle><description>: Solitary fibrous tumour (SFT) is an uncommon mesenchymal neoplasm rarely located in the oral cavity. To characterize further oral SFT, we describe three new cases. Each tumour originated in the buccal mucosa of a middle‐aged/elderly patient. Histological examination showed well‐circumscribed tumours with densely cellular areas alternating with hypocellular areas in a variedly collagenous, vascular stroma. Mast cells were abundant. The spindle‐shaped, neoplastic cells immunostained strongly for CD34 antigen and vimentin and weakly for bcl‐2, but not for epithelial cell markers, α‐smooth muscle actin, or neurofilament or S‐100 proteins. Compatible with the virtual absence of mitoses and of marked nuclear atypia, the overall frequency of proliferating cells expressing Ki‐67 was low. The expression of CD34 was useful in the differential diagnosis. The consistent location in the cheek and expansion of one tumour after local trauma does not preclude a traumatic element in the development of oral SFT.</description><subject>Aged</subject><subject>Antigens, CD34 - analysis</subject><subject>bcl‐2</subject><subject>Biological and medical sciences</subject><subject>Blood Vessels - pathology</subject><subject>CD34</subject><subject>Cell Nucleus - ultrastructure</subject><subject>Collagen</subject><subject>Dentistry</subject><subject>Diagnosis, Differential</subject><subject>Female</subject><subject>histology</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Ki-67 Antigen - analysis</subject><subject>Male</subject><subject>Mast Cells - pathology</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mitosis</subject><subject>Mouth Mucosa - pathology</subject><subject>Mouth Neoplasms - pathology</subject><subject>Neoplasms, Fibrous Tissue - pathology</subject><subject>oral cavity</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>Proto-Oncogene Proteins c-bcl-2 - analysis</subject><subject>solitary fibrous tumour (SFT)</subject><subject>Tumors</subject><subject>Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology</subject><subject>vimentin</subject><subject>Vimentin - analysis</subject><issn>0904-2512</issn><issn>1600-0714</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqNkE1v1DAQhi0EotvCX0BBQtwS7Dix15yoKsqHKhUJOFv-GBOvknixHdrl1-MlK-DIydbMM-_YD0LPCW4Ipt2rXUMYxjXmpGtajHHTCtxh3tw_QJs_nYdog0u5bnvSnqHzlHYYE0478hidEcwZo4Jv0N3nMPqs4qFyXsewpCovU1hiFVyVB6hCVGNl1A-fD68rM_rZm7BXeQhj-OZN6anZVn6aljkMPuVgBph-182gojIZov-psg_zGhgBSlqC9AQ9cmpM8PR0XqCv12-_XL2vb27ffbi6vKkNFYLXgrnOUgs9uK0mjvGedLTnWrut4qLDtrdag9MgWqtZS7lhzG5h2zuicQ-WXqCXa-4-hu8LpCwnnwyMo5qh_FZygvuWC15AsYImhpQiOLmPfipiJMHyaF3u5NGtPLqVR-tytS7vy-yz05JFT2D_mVw1F-DFCVCpyHFRzcanvxwlgrVdwd6s2J0f4fD_D5Afbz-td_oLH9Whpw</recordid><startdate>200004</startdate><enddate>200004</enddate><creator>Lukinmaa, Pirjo‐Liisa</creator><creator>Hietanen, Jarkko</creator><creator>Warfvinge, Gunnar</creator><creator>Sane, Juha</creator><creator>Tuominen, Susanne</creator><creator>Henriksson, Vincent</creator><creator>Larsson, Åke</creator><general>Munksgaard International Publishers</general><general>Blackwell</general><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>7X8</scope></search><sort><creationdate>200004</creationdate><title>Solitary fibrous tumour of the oral cavity: clinicopathological and immunohistochemical characterization of three cases</title><author>Lukinmaa, Pirjo‐Liisa ; Hietanen, Jarkko ; Warfvinge, Gunnar ; Sane, Juha ; Tuominen, Susanne ; Henriksson, Vincent ; Larsson, Åke</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3997-96f4d3de5ef8b1f67514357bbf8a7940d5dbbefbe92db6237c66d8e85f1b05ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Aged</topic><topic>Antigens, CD34 - analysis</topic><topic>bcl‐2</topic><topic>Biological and medical sciences</topic><topic>Blood Vessels - pathology</topic><topic>CD34</topic><topic>Cell Nucleus - ultrastructure</topic><topic>Collagen</topic><topic>Dentistry</topic><topic>Diagnosis, Differential</topic><topic>Female</topic><topic>histology</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Ki-67 Antigen - analysis</topic><topic>Male</topic><topic>Mast Cells - pathology</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mitosis</topic><topic>Mouth Mucosa - pathology</topic><topic>Mouth Neoplasms - pathology</topic><topic>Neoplasms, Fibrous Tissue - pathology</topic><topic>oral cavity</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>Proto-Oncogene Proteins c-bcl-2 - analysis</topic><topic>solitary fibrous tumour (SFT)</topic><topic>Tumors</topic><topic>Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology</topic><topic>vimentin</topic><topic>Vimentin - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lukinmaa, Pirjo‐Liisa</creatorcontrib><creatorcontrib>Hietanen, Jarkko</creatorcontrib><creatorcontrib>Warfvinge, Gunnar</creatorcontrib><creatorcontrib>Sane, Juha</creatorcontrib><creatorcontrib>Tuominen, Susanne</creatorcontrib><creatorcontrib>Henriksson, Vincent</creatorcontrib><creatorcontrib>Larsson, Åke</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Journal of oral pathology & medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lukinmaa, Pirjo‐Liisa</au><au>Hietanen, Jarkko</au><au>Warfvinge, Gunnar</au><au>Sane, Juha</au><au>Tuominen, Susanne</au><au>Henriksson, Vincent</au><au>Larsson, Åke</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Solitary fibrous tumour of the oral cavity: clinicopathological and immunohistochemical characterization of three cases</atitle><jtitle>Journal of oral pathology & medicine</jtitle><addtitle>J Oral Pathol Med</addtitle><date>2000-04</date><risdate>2000</risdate><volume>29</volume><issue>4</issue><spage>186</spage><epage>192</epage><pages>186-192</pages><issn>0904-2512</issn><eissn>1600-0714</eissn><abstract>: Solitary fibrous tumour (SFT) is an uncommon mesenchymal neoplasm rarely located in the oral cavity. To characterize further oral SFT, we describe three new cases. Each tumour originated in the buccal mucosa of a middle‐aged/elderly patient. Histological examination showed well‐circumscribed tumours with densely cellular areas alternating with hypocellular areas in a variedly collagenous, vascular stroma. Mast cells were abundant. The spindle‐shaped, neoplastic cells immunostained strongly for CD34 antigen and vimentin and weakly for bcl‐2, but not for epithelial cell markers, α‐smooth muscle actin, or neurofilament or S‐100 proteins. Compatible with the virtual absence of mitoses and of marked nuclear atypia, the overall frequency of proliferating cells expressing Ki‐67 was low. The expression of CD34 was useful in the differential diagnosis. The consistent location in the cheek and expansion of one tumour after local trauma does not preclude a traumatic element in the development of oral SFT.</abstract><cop>Copenhagen</cop><pub>Munksgaard International Publishers</pub><pmid>10766397</pmid><doi>10.1034/j.1600-0714.2000.290407.x</doi><tpages>7</tpages></addata></record> |
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subjects | Aged Antigens, CD34 - analysis bcl‐2 Biological and medical sciences Blood Vessels - pathology CD34 Cell Nucleus - ultrastructure Collagen Dentistry Diagnosis, Differential Female histology Humans Immunohistochemistry Ki-67 Antigen - analysis Male Mast Cells - pathology Medical sciences Middle Aged Mitosis Mouth Mucosa - pathology Mouth Neoplasms - pathology Neoplasms, Fibrous Tissue - pathology oral cavity Otorhinolaryngology. Stomatology Proto-Oncogene Proteins c-bcl-2 - analysis solitary fibrous tumour (SFT) Tumors Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology vimentin Vimentin - analysis |
title | Solitary fibrous tumour of the oral cavity: clinicopathological and immunohistochemical characterization of three cases |
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