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A Rare Malignancy in an Adolescent: Desmoplastic Small Round Cell Tumor

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dc.contributor.author Güleç, Mert Doğan
dc.contributor.author Sigirci, Ahmet
dc.contributor.author Akyay, Arzu
dc.contributor.author Uğuralp, Sema
dc.contributor.author Güvenç, Merve Nur
dc.date.accessioned 2022-12-06T09:22:33Z
dc.date.available 2022-12-06T09:22:33Z
dc.date.issued 2021
dc.identifier.citation DOĞAN G, SIĞIRCI A, AKYAY A, UĞURALP S, GÜVENÇ M (2021). A Rare Malignancy in an Adolescent: Desmoplastic Small Round Cell Tumor. Türkiye Klinikleri Journal of Case Reports, 29(1), 45 - 50. 10.5336/caserep.2020-77722 en_US
dc.identifier.uri https://search.trdizin.gov.tr/yayin/detay/491867/a-rare-malignancy-in-an-adolescent-desmoplastic-small-round-cell-tumor
dc.identifier.uri http://hdl.handle.net/11616/85645
dc.description.abstract Desmoplastic small round cell tumor (DSRCT) is a very rare condition. The peritoneal cavity is most frequently involved. Ab- dominopelvic computed tomography findings include omental or serosal masses, a dominant tumor, tumor calcification, liver metastasis, ab- dominal lymphadenopathies, acid and intestinal obstruction. A complete surgical resection including systemic implants, systemicchemotherapy and radiotherapy, hyperthermic intraperitoneal chemotherapy and stem cell transplantation can be used in the treatment of the disease. Since this tumor is very rare, we could only find case reports or a few large numbered patient series in the literature. Here in this case report, we aim to discuss the imaging findings of an adolescent patient at the time of admission. en_US
dc.language.iso eng en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.title A Rare Malignancy in an Adolescent: Desmoplastic Small Round Cell Tumor en_US
dc.type article en_US
dc.relation.ispartof Türkiye Klinikleri Journal of Case Reports en_US
dc.department İnönü Üniversitesi en_US


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