Publication:
A rare primary pulmonary tumor in children; Rhabdomyosarcoma

dc.contributor.authorsTürkkan E., Berrak S.G., Canpolat C., Ergüven M., Abacioglu U., Fedakar A.
dc.date.accessioned2022-03-28T14:58:10Z
dc.date.accessioned2026-01-11T07:59:22Z
dc.date.available2022-03-28T14:58:10Z
dc.date.issued2010
dc.description.abstractAfter 4 cycles of chemotherapy to treat a locally advanced tumor CT showed minimal regression of the tumor. As the locally advanced tumor was still adjacent to vital structures at the 12th week of chemotherapy, radiation therapy was given to achieve local control. The treatment was stopped after 3 additional VAC courses following radiotherapy because of continued tumor progression. The patient died nine months after the initial diagnosis. We discussed prognostic features of primary pulmonary RMS and recommend that it should be considered in the differential diagnosis of children with persistent pulmonary symptoms or chest X-ray abnormalities.
dc.identifier.issn10191941
dc.identifier.pubmedMMJOF
dc.identifier.urihttps://hdl.handle.net/11424/256521
dc.language.isoeng
dc.relation.ispartofMarmara Medical Journal
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectChild
dc.subjectPrimary
dc.subjectPulmonary
dc.subjectRabdomyosarcoma
dc.titleA rare primary pulmonary tumor in children; Rhabdomyosarcoma
dc.typearticle
dspace.entity.typePublication
oaire.citation.issue1
oaire.citation.titleMarmara Medical Journal
oaire.citation.volume23

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