Giant solitary fibrous tumour of the liver
Identifieur interne : 003C71 ( Pmc/Checkpoint ); précédent : 003C70; suivant : 003C72Giant solitary fibrous tumour of the liver
Auteurs : Türkan Terkivatan [Pays-Bas] ; Mike Kliffen [Pays-Bas] ; Johannes Hw De Wilt [Pays-Bas] ; Albertus N. Van Geel [Pays-Bas] ; Alexander Mm Eggermont [Pays-Bas] ; Cornelis Verhoef [Pays-Bas]Source :
- World Journal of Surgical Oncology [ 1477-7819 ] ; 2006.
Abstract
Solitary fibrous tumour (SFT) is an uncommon mesenchymal neoplasm that most frequently affects the pleura, although it has been reported with increasing frequency in various other sites such as in the peritoneum, pericardium and in non-serosal sites such as lung parenchyma, upper respiratory tract, orbit, thyroid, parotid gland, or thymus. Liver parenchyma is rarely affected. Clinically, SFTs cause symptoms after having reached a certain size or when vital structures are involved. In recent years, SFTs are more often identified and distinguished from other tumours with a similar appearance due to the availability of characteristic immunohistochemical markers.
In this manuscript we report the case of a large tumour of the liver, which was histologically diagnosed as a SFT, and showed involvement of a single hepatic segment. Because of the patient's presentation and clinical course, it may represent a radiation-induced lesion.
When a SFT has been diagnosed, surgery is the treatment of choice. The small number of patients with a SFT of the liver and its unknown natural behaviour creates the need to a careful registration and follow-up of all identified cases
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DOI: 10.1186/1477-7819-4-81
PubMed: 17118185
PubMed Central: 1661593
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<front><div type="abstract" xml:lang="en"><sec><title>Background</title>
<p>Solitary fibrous tumour (SFT) is an uncommon mesenchymal neoplasm that most frequently affects the pleura, although it has been reported with increasing frequency in various other sites such as in the peritoneum, pericardium and in non-serosal sites such as lung parenchyma, upper respiratory tract, orbit, thyroid, parotid gland, or thymus. Liver parenchyma is rarely affected. Clinically, SFTs cause symptoms after having reached a certain size or when vital structures are involved. In recent years, SFTs are more often identified and distinguished from other tumours with a similar appearance due to the availability of characteristic immunohistochemical markers.</p>
</sec>
<sec><title>Case presentation</title>
<p>In this manuscript we report the case of a large tumour of the liver, which was histologically diagnosed as a SFT, and showed involvement of a single hepatic segment. Because of the patient's presentation and clinical course, it may represent a radiation-induced lesion.</p>
</sec>
<sec><title>Conclusion</title>
<p>When a SFT has been diagnosed, surgery is the treatment of choice. The small number of patients with a SFT of the liver and its unknown natural behaviour creates the need to a careful registration and follow-up of all identified cases</p>
</sec>
</div>
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<front><journal-meta><journal-id journal-id-type="nlm-ta">World J Surg Oncol</journal-id>
<journal-title>World Journal of Surgical Oncology</journal-title>
<issn pub-type="epub">1477-7819</issn>
<publisher><publisher-name>BioMed Central</publisher-name>
<publisher-loc>London</publisher-loc>
</publisher>
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<article-meta><article-id pub-id-type="pmid">17118185</article-id>
<article-id pub-id-type="pmc">1661593</article-id>
<article-id pub-id-type="publisher-id">1477-7819-4-81</article-id>
<article-id pub-id-type="doi">10.1186/1477-7819-4-81</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Case Report</subject>
</subj-group>
</article-categories>
<title-group><article-title>Giant solitary fibrous tumour of the liver</article-title>
</title-group>
<contrib-group><contrib id="A1" contrib-type="author"><name><surname>Terkivatan</surname>
<given-names>Türkan</given-names>
</name>
<xref ref-type="aff" rid="I1">1</xref>
<email>t.terkivatan@erasmusmc.nl</email>
</contrib>
<contrib id="A2" contrib-type="author"><name><surname>Kliffen</surname>
<given-names>Mike</given-names>
</name>
<xref ref-type="aff" rid="I2">2</xref>
<email>m.kliffen@erasmusmc.nl</email>
</contrib>
<contrib id="A3" contrib-type="author"><name><surname>de Wilt</surname>
<given-names>Johannes HW</given-names>
</name>
<xref ref-type="aff" rid="I1">1</xref>
<email>j.h.w.dewilt@erasmusmc.nl</email>
</contrib>
<contrib id="A4" contrib-type="author"><name><surname>van Geel</surname>
<given-names>Albertus N</given-names>
</name>
<xref ref-type="aff" rid="I1">1</xref>
<email>a.n.vangeel@erasmusmc.nl</email>
</contrib>
<contrib id="A5" contrib-type="author"><name><surname>Eggermont</surname>
<given-names>Alexander MM</given-names>
</name>
<xref ref-type="aff" rid="I1">1</xref>
<email>a.m.m.eggermont@erasmusmc.nl</email>
</contrib>
<contrib id="A6" corresp="yes" contrib-type="author"><name><surname>Verhoef</surname>
<given-names>Cornelis</given-names>
</name>
<xref ref-type="aff" rid="I1">1</xref>
<email>c.verhoef@erasmusmc.nl</email>
</contrib>
</contrib-group>
<aff id="I1"><label>1</label>
Department of Surgical Oncology, Erasmus University Medical Center, Daniel den Hoed Cancer Center, Rotterdam, The Netherlands</aff>
<aff id="I2"><label>2</label>
Department of Pathology, Erasmus University Medical Center, Daniel den Hoed Cancer Center, Rotterdam, The Netherlands</aff>
<pub-date pub-type="collection"><year>2006</year>
</pub-date>
<pub-date pub-type="epub"><day>21</day>
<month>11</month>
<year>2006</year>
</pub-date>
<volume>4</volume>
<fpage>81</fpage>
<lpage>81</lpage>
<ext-link ext-link-type="uri" xlink:href="http://www.wjso.com/content/4/1/81"></ext-link>
<history><date date-type="received"><day>5</day>
<month>4</month>
<year>2006</year>
</date>
<date date-type="accepted"><day>21</day>
<month>11</month>
<year>2006</year>
</date>
</history>
<permissions><copyright-statement>Copyright © 2006 Terkivatan et al; licensee BioMed Central Ltd.</copyright-statement>
<copyright-year>2006</copyright-year>
<copyright-holder>Terkivatan et al; licensee BioMed Central Ltd.</copyright-holder>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/2.0"><p>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/2.0"></ext-link>
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</p>
<pmc-comment>
Terkivatan
Türkan
t.terkivatan@erasmusmc.nl
Giant solitary fibrous tumour of the liver
2006 World Journal of Surgical Oncology 4(1): 81-. (2006) 1477-7819(2006)4:1<81> urn:ISSN:1477-7819 </pmc-comment>
</license>
</permissions>
<abstract><sec><title>Background</title>
<p>Solitary fibrous tumour (SFT) is an uncommon mesenchymal neoplasm that most frequently affects the pleura, although it has been reported with increasing frequency in various other sites such as in the peritoneum, pericardium and in non-serosal sites such as lung parenchyma, upper respiratory tract, orbit, thyroid, parotid gland, or thymus. Liver parenchyma is rarely affected. Clinically, SFTs cause symptoms after having reached a certain size or when vital structures are involved. In recent years, SFTs are more often identified and distinguished from other tumours with a similar appearance due to the availability of characteristic immunohistochemical markers.</p>
</sec>
<sec><title>Case presentation</title>
<p>In this manuscript we report the case of a large tumour of the liver, which was histologically diagnosed as a SFT, and showed involvement of a single hepatic segment. Because of the patient's presentation and clinical course, it may represent a radiation-induced lesion.</p>
</sec>
<sec><title>Conclusion</title>
<p>When a SFT has been diagnosed, surgery is the treatment of choice. The small number of patients with a SFT of the liver and its unknown natural behaviour creates the need to a careful registration and follow-up of all identified cases</p>
</sec>
</abstract>
</article-meta>
</front>
</pmc>
<affiliations><list><country><li>Pays-Bas</li>
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<name sortKey="De Wilt, Johannes Hw" sort="De Wilt, Johannes Hw" uniqKey="De Wilt J" first="Johannes Hw" last="De Wilt">Johannes Hw De Wilt</name>
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<name sortKey="Kliffen, Mike" sort="Kliffen, Mike" uniqKey="Kliffen M" first="Mike" last="Kliffen">Mike Kliffen</name>
<name sortKey="Van Geel, Albertus N" sort="Van Geel, Albertus N" uniqKey="Van Geel A" first="Albertus N" last="Van Geel">Albertus N. Van Geel</name>
<name sortKey="Verhoef, Cornelis" sort="Verhoef, Cornelis" uniqKey="Verhoef C" first="Cornelis" last="Verhoef">Cornelis Verhoef</name>
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