Results 31 to 40 of about 103,219 (202)

Primary localized retroperitoneal sarcomas: report from Slovenian sarcoma referral center

open access: yesWorld Journal of Surgical Oncology, 2020
Background Sarcoma patients should be treated in high volume referral sarcoma centers. Compartmental resection is proposed as the best treatment option in retroperitoneal sarcoma patients.
Marko Novak   +4 more
doaj   +1 more source

Retrospective quality of life study in patients with retroperitoneal sarcoma in an Asian population

open access: yesHealth and Quality of Life Outcomes, 2020
Background Retroperitoneal sarcoma represents 15% of sarcomas. The mainstay of treatment is surgery where a majority of patients require multi-visceral resections that may significantly impact their quality of life (QOL) following surgery.
Hui Jun Lim   +8 more
doaj   +1 more source

Undifferentiated pleomorphic sarcoma of the retroperitoneum mimicking a cortisol‐ and catecholamine‐secreting adrenal tumor

open access: yesIJU Case Reports, 2022
Introduction Retroperitoneal tumors with endocrine abnormalities are suspected to be functional adrenal tumors. Retroperitoneal soft tissue sarcomas are rare tumors, without endocrine potential.
Takayoshi Fuu   +2 more
doaj   +1 more source

Simultaneous Renal Cell Carcinoma and Giant Retroperitoneal Liposarcoma Involving Small Intestine

open access: yesCase Reports in Surgery, 2016
Background. The concomitant occurrence of a renal cell carcinoma and retroperitoneal sarcoma is extremely rare with only few cases being reported. Methods.
Aleksandr A. Reznichenko
doaj   +1 more source

3- RETROPERITONEAL SARCOMA [PDF]

open access: yesBasrah Journal of Surgery, 2011
Review Article RETROPERITONEAL SARCOMA Majeed H Alwan MBChB, FRCSEd, FRACS, FACS, Gastrointestinal and General Surgeon, Tauranga Hospital, Tauranga, New Zealand. E-mail: majeedalwan@xtra.co.nz Abstract Retroperitoneal sarcoma (RPS) is a rare tumour.
Majeed H Alwan
doaj   +1 more source

Practical Management of Adult Ultra-Rare Primary Retroperitoneal Soft Tissue Sarcoma: A Focus on Perivascular Epithelioid Tumours and Extraosseous Ewing Sarcoma

open access: yesCurrent Oncology, 2023
With the exception of well-differentiated liposarcoma, dedifferentiated liposarcoma, leiomyosarcoma, solitary fibrous tumour, malignant peripheral nerve sheath tumour, and undifferentiated pleomorphic sarcoma, the majority of the ≈70 histologic subtypes ...
Sameer S. Apte   +3 more
doaj   +1 more source

Recent Progress in the Management of Retroperitoneal Sarcoma [PDF]

open access: yes, 2002
Retroperitoneal sarcomas (RPS) are rare tumours that typically present late and carry a poor prognosis even following grossly complete resection. In an attempt to improve the outlook for patients with RPS, sarcoma specialists have employed various ...
Couture, Jean   +11 more
core   +2 more sources

Study on preoperative radiotherapy in conversion therapy for patients with primary retroperitoneal soft tissue sarcoma difficult to resect or unresectable [PDF]

open access: yesWaike lilun yu shijian, 2022
Objective: To investigate the effect of preoperative radiotherapy in the patients with primary retroperitoneal soft tissue sarcoma difficult to resect or unresectable and recognize the results of radiotherapy associated with resection and the effect of ...
PAN Xiangou, ZHANG Li, HOU Jiazhou, DU Shisuo, ZENG Zhaochong, WANG Binliang
doaj   +1 more source

A novel strategy for reconstruction of the renal vein and inferior vena cava (IVC) after resection of IVC leiomyosarcoma-a case report

open access: yesAnnals of Vascular Surgery - Brief Reports and Innovations
s: A 30-year-old male patient diagnosed leiomyosarcoma originating from level II of inferior vena cava (IVC). The tumor involved IVC, right renal vein, the confluence of left renal vein and IVC, and the dorsal part of pancreatic head. An enbloc resection
Chentao LV   +8 more
doaj   +1 more source

Retroperitoneal soft tissue sarcoma: prognostic factors and therapeutic approaches

open access: yes, 2008
AIMS AND BACKGROUND: Retroperitoneal sarcomas are a rare group of malignant soft tissue tumors with a generally poor prognosis. The aim of the study was to assess clinical, pathological and treatment-related factors affecting prognosis in patients with ...
Alessandra Ferro   +18 more
core   +1 more source

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