Retroperitoneal soft tissue Sarcomas: retrospective cohort study

dc.authorid0000-0001-9493-4055
dc.authorid0000-0003-2935-8463
dc.authorid0000-0002-1403-7643
dc.authorid0000-0003-1708-0003
dc.contributor.authorOzsoy, Mehmet Sait
dc.contributor.authorEkinci, Özgür
dc.contributor.authorAcar, Mehmet
dc.contributor.authorLeblebici, Metin
dc.contributor.authorIsik, Arda
dc.contributor.authorYildirim, Ayse Nur Toksoz
dc.contributor.authorGündüz, Nesrin
dc.date.accessioned2025-05-10T19:36:34Z
dc.date.issued2022
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractObjective: Soft Tissue Sarcomas are rare mesenchymal tumors with many subtypes. Clean margin wide resection is recommended for treatment.In this study, the location, histopathological features, clinical and demographic features, recurrence and prognosis of retroperitoneal sarcomas were investigated. Methods: The demographic, histopathological and immunohistochemical data of 18 patients who were operated on with the diagnosis of retroperitoneal mass between March 2016 and June 2021 were evaluated retrospectively. Results: 18 patients were included in the study. 10 patients were male and 8 patients were female. The mean age was 57 (23-81), the median age was 55. While 14 patients were primary sarcoma, 4 patients were recurrent sarcoma. The most common complaint was abdominal pain with 38,87%. The average follow-up time was 26 (0-55) months. The postoperative mean hospitalstay was 5,83 (2-8) days. The average size of the tumor was 19,81 (6,5-36) cm. A total of 8 different histopathological sarcoma types were detected. The most common histology was Dedifferentiated Liposarcoma (44,45%). R0 resection in 10 patients, R1 resection in 6 patients and R2 resection in 2 patient were performed. Organ resection was performed in 6 patients due to organ invasion. During follow-up, 10 patients had a local recurrence and underwent reresection and 6 patients died. The 30-day mortality number was 0. The mean time to detect relapse was 9,3 (1-55) months. Metastasis developed in 2 (11, 11%) patients. Conclusion:Although we are a low-volume hospital for retroperitoneal sarcomas, our results are similar to those in the literature.
dc.identifier.doi10.3329/bjms.v21i4.60258
dc.identifier.endpage835
dc.identifier.issn2223-4721
dc.identifier.issn2076-0299
dc.identifier.issue4
dc.identifier.scopus2-s2.0-85137800187
dc.identifier.scopusqualityQ2
dc.identifier.startpage829
dc.identifier.urihttps://doi.org/10.3329/bjms.v21i4.60258
dc.identifier.urihttps://hdl.handle.net/20.500.14730/9233
dc.identifier.volume21
dc.identifier.wosWOS:000869502700020
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherIbn Sina Trust
dc.relation.ispartofBangladesh Journal of Medical Science
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250302
dc.subjectSoft tissue sarcoma
dc.subjectRetroperitoneal Tumor
dc.subjectSurgery
dc.subjectMultidisciplinary Sarcoma Team
dc.titleRetroperitoneal soft tissue Sarcomas: retrospective cohort study
dc.typeArticle

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