Solitary Fibrous Tumor - Less Common Neoplasms of the Pleural Cavity

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11140%2F17%3A10338048" target="_blank" >RIV/00216208:11140/17:10338048 - isvavai.cz</a>
Alternative codes found
RIV/00669806:_____/17:10338048
Result on the web
<a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347482/" target="_blank" >https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347482/</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.5761/atcs.oa.16-00108" target="_blank" >10.5761/atcs.oa.16-00108</a>

Result language
angličtina
Original language name
Solitary Fibrous Tumor - Less Common Neoplasms of the Pleural Cavity
Original language description
Solitary fibrous tumors (SFT) represent a heterogeneous group of primary pleural neoplasms with a low incidence rate and of which the biological origin, which consists of mesenchymal cells, is uncertain. The authors present herewith a retrospective analysis of 22 patients with SFTs who were diagnosed and surgically treated between the years 2000-2015. The gold standart of SFT treatment is radical surgical removal; however, patients at risk of recurrence require additional follow-ups. The results of adjuvant therapy in recurrent and malignant forms of SFTs are the subject of discussion and further study.
Czech name
—
Czech description
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Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30212 - Surgery

Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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