Orbital rhabdomyosarcoma: Review

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dc.contributor.authorPalamar, Melis
dc.contributor.authorKorkmaz, İlayda
dc.contributor.authorYaman, Banu
dc.contributor.authorCeylan, Naim
dc.contributor.authorKantar, Mehmet
dc.contributor.authorKamer, Serra
dc.date.accessioned2024-08-25T18:51:53Z
dc.date.available2024-08-25T18:51:53Z
dc.date.issued2023
dc.departmentEge Üniversitesien_US
dc.description.abstractOrbital rhabdomyosarcoma is the most common malignant orbital tumor of child-hood originating from mesenchymal cells. The presenting symptom is usually acute onset unilateral proptosis. The rapidly progressive course of the findings may resemble infectious and inflammatory orbital diseases. Radiological imaging and histopathological examinations are crucial for differential diagnosis. The main goal of treatment with a multidisciplinary approach is to control both local and distant spread of the tumor and to prevent further damage. With the introduction of chemotherapy and radiotherapy in the treatment, the overall survival rate has in-creased. Thus, aggressive surgical approach for complete removal of the tumor has been abandoned.en_US
dc.identifier.doi10.14744/eer.2022.02996
dc.identifier.endpage31en_US
dc.identifier.issn2757-8135
dc.identifier.issn2757-9816
dc.identifier.issue1en_US
dc.identifier.startpage26en_US
dc.identifier.trdizinid1178336en_US
dc.identifier.urihttps://doi.org/10.14744/eer.2022.02996
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/1178336
dc.identifier.urihttps://hdl.handle.net/11454/102752
dc.identifier.volume3en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofEuropean eye researchen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.snmz20240825_Gen_US
dc.titleOrbital rhabdomyosarcoma: Reviewen_US
dc.typeArticleen_US

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