Bilateral Spontaneous Pneumothorax due to Pulmonary Metastasis of Synovial Sarcoma: A Case Report

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dc.contributor.authorAvci, Alper
dc.contributor.authorEren, Sevval
dc.date.accessioned2024-04-24T17:27:31Z
dc.date.available2024-04-24T17:27:31Z
dc.date.issued2011
dc.departmentDicle Üniversitesien_US
dc.description.abstractSpontaneous pneumothorax is a rarely seen complication in metastatic pulmonary diseases. It could be the first symptom and might be seen in the post chemotherapy period. We here report a 20-year-old male with surgically treated-bilaterally spontaneous pneumothorax who had hypopharyngeal synovial sarcoma initially and had been treated with surgery and chemotherapy. We emphasised that spontaneous pneumothorax could be caused by pulmonary mature metastais of synovial sarcoma, as a result of air leakage. Surgical treatment such as metastasectomy and pulmonary paranchimal repair and intraoperatively chemical pleurodesis would be requireden_US
dc.identifier.doi10.5152/ttd.2011.19
dc.identifier.endpage83en_US
dc.identifier.issn1302-7808
dc.identifier.issn1308-5387
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-80052072015
dc.identifier.scopusqualityQ4
dc.identifier.startpage81en_US
dc.identifier.urihttps://doi.org/10.5152/ttd.2011.19
dc.identifier.urihttps://hdl.handle.net/11468/20013
dc.identifier.volume12en_US
dc.identifier.wosWOS:000421718900010
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isotren_US
dc.publisherBilimsel Tip Publishing Houseen_US
dc.relation.ispartofTurkish Thoracic Journal
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSynovial Sarcomaen_US
dc.subjectPulmonary Metastasisen_US
dc.subjectSpontaneous Pneumothoraxen_US
dc.titleBilateral Spontaneous Pneumothorax due to Pulmonary Metastasis of Synovial Sarcoma: A Case Reporten_US
dc.titleBilateral Spontaneous Pneumothorax due to Pulmonary Metastasis of Synovial Sarcoma: A Case Report
dc.typeArticleen_US

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