Serveur d'exploration sur le patient édenté (maquette)

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Primary intraosseous squamous cell carcinoma of the maxilla possibly arising from an infected residual cyst: A case report

Identifieur interne : 000723 ( Pmc/Curation ); précédent : 000722; suivant : 000724

Primary intraosseous squamous cell carcinoma of the maxilla possibly arising from an infected residual cyst: A case report

Auteurs : Shintaro Sukegawa [Japon] ; Hidenobu Matsuzaki [Japon] ; Naoki Katase [Japon] ; Takahiro Kanno [Japon] ; Toshiko Mandai [Japon] ; Yuka Takahashi [Japon] ; Jun-Ichi Asaumi [Japon] ; Yoshihiko Furuki [Japon]

Source :

RBID : PMC:4246683

Abstract

Primary intraosseous squamous cell carcinoma (PIOSCC) is a rare type of odontogenic carcinoma arising from the jawbone. Odontogenic cysts are true cysts that arise from the dental epithelium, which is associated with tooth formation. The epithelial lining of odontogenic cysts has the potential to transform into various types of odontogenic tumor; however, this transformation from an odontogenic cyst to a malignant tumor is rare. The definitive diagnosis for PIOSCC generally requires the observation of either features of squamous cell carcinoma (SCC) within the jawbone that are distinct from direct invasion from the surface oral epithelium, or evidence of SCC arising from odontogenic epithelium and from tumors that have metastasized to the jawbone from distant sites. In the present study, a case of PIOSCC of the maxilla is presented, which, based on the results of computed tomography and the clinical course, was hypothesized to have originated from an infected residual cyst.


Url:
DOI: 10.3892/ol.2014.2644
PubMed: 25435946
PubMed Central: 4246683

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PMC:4246683

Le document en format XML

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<p>Primary intraosseous squamous cell carcinoma (PIOSCC) is a rare type of odontogenic carcinoma arising from the jawbone. Odontogenic cysts are true cysts that arise from the dental epithelium, which is associated with tooth formation. The epithelial lining of odontogenic cysts has the potential to transform into various types of odontogenic tumor; however, this transformation from an odontogenic cyst to a malignant tumor is rare. The definitive diagnosis for PIOSCC generally requires the observation of either features of squamous cell carcinoma (SCC) within the jawbone that are distinct from direct invasion from the surface oral epithelium, or evidence of SCC arising from odontogenic epithelium and from tumors that have metastasized to the jawbone from distant sites. In the present study, a case of PIOSCC of the maxilla is presented, which, based on the results of computed tomography and the clinical course, was hypothesized to have originated from an infected residual cyst.</p>
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<contrib contrib-type="author">
<name>
<surname>SUKEGAWA</surname>
<given-names>SHINTARO</given-names>
</name>
<xref ref-type="aff" rid="af1-ol-09-01-0131">1</xref>
<xref ref-type="corresp" rid="c1-ol-09-01-0131"></xref>
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<surname>MATSUZAKI</surname>
<given-names>HIDENOBU</given-names>
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<xref ref-type="aff" rid="af2-ol-09-01-0131">2</xref>
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<surname>KATASE</surname>
<given-names>NAOKI</given-names>
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<xref ref-type="aff" rid="af3-ol-09-01-0131">3</xref>
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<name>
<surname>KANNO</surname>
<given-names>TAKAHIRO</given-names>
</name>
<xref ref-type="aff" rid="af1-ol-09-01-0131">1</xref>
<xref ref-type="aff" rid="af4-ol-09-01-0131">4</xref>
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<name>
<surname>MANDAI</surname>
<given-names>TOSHIKO</given-names>
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<xref ref-type="aff" rid="af1-ol-09-01-0131">1</xref>
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<name>
<surname>TAKAHASHI</surname>
<given-names>YUKA</given-names>
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<xref ref-type="aff" rid="af1-ol-09-01-0131">1</xref>
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<name>
<surname>ASAUMI</surname>
<given-names>JUN-ICHI</given-names>
</name>
<xref ref-type="aff" rid="af2-ol-09-01-0131">2</xref>
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<contrib contrib-type="author">
<name>
<surname>FURUKI</surname>
<given-names>YOSHIHIKO</given-names>
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<xref ref-type="aff" rid="af1-ol-09-01-0131">1</xref>
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Division of Oral and Maxillofacial Surgery, Kagawa Prefectural Central Hospital, Takamatsu, Kagawa 760-8557, Japan</aff>
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<label>2</label>
Department of Oral Diagnosis and Dentomaxillofacial Radiology, Okayama University Hospital, Okayama 700-8558, Japan</aff>
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Department of Molecular and Developmental Biology, Kawasaki Medical School, Kurashiki, Okayama 701-0192, Japan</aff>
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Department of Oral and Maxillofacial Surgery, Shimane University Faculty of Medicine, Izumo, Shimane 693-8501, Japan</aff>
<author-notes>
<corresp id="c1-ol-09-01-0131">Correspondence to: Dr Shintaro Sukegawa, Division of Oral and Maxillofacial Surgery, Kagawa Prefectural Central Hospital, 1-2-1 Asahi-cho, Takamatsu, Kagawa 760-8557, Japan, E-mail:
<email>gouwan19@gmail.com</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub">
<month>1</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="epub">
<day>27</day>
<month>10</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>27</day>
<month>10</month>
<year>2014</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on the . </pmc-comment>
<volume>9</volume>
<issue>1</issue>
<fpage>131</fpage>
<lpage>135</lpage>
<history>
<date date-type="received">
<day>06</day>
<month>3</month>
<year>2014</year>
</date>
<date date-type="accepted">
<day>15</day>
<month>8</month>
<year>2014</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2015, Spandidos Publications</copyright-statement>
<copyright-year>2015</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/3.0">
<license-p>This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.</license-p>
</license>
</permissions>
<abstract>
<p>Primary intraosseous squamous cell carcinoma (PIOSCC) is a rare type of odontogenic carcinoma arising from the jawbone. Odontogenic cysts are true cysts that arise from the dental epithelium, which is associated with tooth formation. The epithelial lining of odontogenic cysts has the potential to transform into various types of odontogenic tumor; however, this transformation from an odontogenic cyst to a malignant tumor is rare. The definitive diagnosis for PIOSCC generally requires the observation of either features of squamous cell carcinoma (SCC) within the jawbone that are distinct from direct invasion from the surface oral epithelium, or evidence of SCC arising from odontogenic epithelium and from tumors that have metastasized to the jawbone from distant sites. In the present study, a case of PIOSCC of the maxilla is presented, which, based on the results of computed tomography and the clinical course, was hypothesized to have originated from an infected residual cyst.</p>
</abstract>
<kwd-group>
<kwd>primary intraosseous squamous cell carcinoma</kwd>
<kwd>residual cyst</kwd>
<kwd>computed tomography</kwd>
</kwd-group>
</article-meta>
</front>
<floats-group>
<fig id="f1-ol-09-01-0131" orientation="portrait" position="float">
<label>Figure 1</label>
<caption>
<p>(A) Marginal facial asymmetry was observed on the left side of the patient’s face. (B and C) Intraoral images were captured showing a large mass located in the buccal and palatal aspect of the edentulous alveolus of the left maxilla, in the area between the second premolar and the first molar. The mucosal surface was covered with rough hemorrhagic papules, which were pink-red in color.</p>
</caption>
<graphic xlink:href="OL-09-01-0131-g00"></graphic>
</fig>
<fig id="f2-ol-09-01-0131" orientation="portrait" position="float">
<label>Figure 2</label>
<caption>
<p>A panoramic radiograph revealed a dome-shaped radiopaque mass with well-defined margins extending from the left maxilla to the maxillary sinus.</p>
</caption>
<graphic xlink:href="OL-09-01-0131-g01"></graphic>
</fig>
<fig id="f3-ol-09-01-0131" orientation="portrait" position="float">
<label>Figure 3</label>
<caption>
<p>Computed tomography images. (A) Axial soft tissue window images revealed a cystic lesion extending from the left maxillary alveolar area to the maxillary sinus. (B and C) Axial and coronal bone window images revealed the thickened floor of the antrum, which was elevated. (C) A section of the elevated sinus floor was destroyed.</p>
</caption>
<graphic xlink:href="OL-09-01-0131-g02"></graphic>
</fig>
<fig id="f4-ol-09-01-0131" orientation="portrait" position="float">
<label>Figure 4</label>
<caption>
<p>(A) Axial 18
<sup>F</sup>
-fluorodeoxyglucose positron emission tomography (FDG-PET)/computed tomography revealed FDG accumulation in the lesion in the left maxilla (maximum standardized uptake value, 12.2). (B) No other abnormal FDG accumulation was detected elsewhere by FDG-PET.</p>
</caption>
<graphic xlink:href="OL-09-01-0131-g03"></graphic>
</fig>
<fig id="f5-ol-09-01-0131" orientation="portrait" position="float">
<label>Figure 5</label>
<caption>
<p>Histopathological observations. (A) The tumor mass was located in the center of the maxilla and extended to the surface epithelium. The epithelium of the maxillary sinus was not involved. (B) The tumor cells formed atypical squamous epithelium, exhibiting features of squamous cell carcinoma (magnification, ×2). (C) The surface of the mass was covered by non-cancerous oral mucosa with ulcers, indicating an intraosseous origin (magnification, ×2).</p>
</caption>
<graphic xlink:href="OL-09-01-0131-g04"></graphic>
</fig>
</floats-group>
</pmc>
</record>

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