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Multifocal Retroperitoneal Sarcoma [PDF]
Case Reports in Surgery, 2013 Introduction. Retroperitoneal sarcomas comprise a small proportion of all soft tissue sarcomas, and multiple factors influence their clinical behavior.
Theodosios Theodosopoulos +6 more
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Preoperative Inflammatory Status and Postoperative Morbidity in Patients With Primary Retroperitoneal Sarcoma [PDF]
Cancer MedicineBackground The role of preoperative inflammatory markers in predicting postoperative outcomes has been investigated in different types of cancer. However, little is known about retroperitoneal sarcoma (RPS).
Pia van derLaan +11 more
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The Role of Surgery in Oligometastatic Retroperitoneal Sarcoma [PDF]
Current Oncology, 2023 Retroperitoneal sarcomas are extremely rare, comprising
Lindsay A. Janes, Christina V. Angeles
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Retroperitoneal sarcomas [PDF]
Cancer Imaging, 2005 Retroperitoneal sarcomas are rare neoplasms. CT or MR imaging is performed in patients with these tumors to detect local extent and distant metastases of the tumor and for preoperative surgical planning. Most sarcomas cannot be characterized as to cell type with CT or MR, with the exceptions being liposarcomas and intracaval leiomyosarcomas.
Francis, Isaac R +3 more
openaire +4 more sources
Surveillance Post Surgery for Retroperitoneal Soft Tissue Sarcoma
Current Oncology, 2023 Complete en bloc surgical resection offers the best opportunity for the cure of primary retroperitoneal sarcomas (RPS). The potential for disease recurrence, in the form of both loco-regional recurrence and distant metastases, underpins the rationale for
John Whitaker +3 more
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Retroperitoneal sarcomas [PDF]
Surgical Oncology Clinics of North America, 2003 Retroperitoneal sarcomas comprise a rare, heterogeneous group of neoplasms. Routine workup should include the patient's medical history, a physical examination, and helical CT of the abdomen and pelvis, with selective use of MRI and preoperative tissue sampling. The primary treatment is complete surgical resection with a rim of normal tissue.
Toni, Ferrario +1 more
openaire +4 more sources
European Journal of Medical Research, 2022 Background Desmoids are rare fibroblastic tumours whose treatment in any individual case presents a persistent challenge. We endeavoured to evaluate various clinicopathological factors contributing to tumour behaviour.
Misbah Khan +3 more
doaj +1 more source
Retroperitoneal synovial sarcoma presenting as paraneoplastic hypoglycaemia [PDF]
Journal of Clinical and Scientific Research, 2015 Synovial sarcoma is a well-recognized malignant mesenchymal neoplasm. Primary retroperitoneal synovial sarcoma is extremely rare and has poor prognosis. There are sparse reports in the literature on the secretory synovial sarcomas.
Reddy VV +4 more
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A Large Primary Retroperitoneal Synovial Sarcoma: A Case Report of a Huge Malignant Tumor [PDF]
Iranian Journal of Medical Sciences, 2022 Synovial Sarcoma (SS) is a rare soft-tissue malignancy. Only about 15% of SS originates from the retroperitoneum. Retroperitoneal SS (RSS) is usually diagnosed incidentally due to the anatomy of the retroperitoneum. The most common complaints of patients
Anahita Ansari Djafari +5 more
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Clinical Case Reports, 2023 Retroperitoneal sarcoma is relatively uncommon. We share our experience in encountering retroperitoneal sarcoma with vascular and urethral adhesion in a 46‐year‐old woman.
Setareh Akhavan +5 more
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