Results 21 to 30 of about 103,219 (202)

Retroperitoneal Sarcomas [PDF]

open access: yesCancer Control, 2005
The evaluation and treatment of retroperitoneal sarcomas are challenging because the tumors are relatively rare and frequently present with advanced disease in an anatomically complex location.We reviewed the literature on experience in the management of retroperitoneal sarcomas, and we present our own experience in the treatment of these tumors.The ...
T Christopher, Windham   +1 more
openaire   +4 more sources

Retroperitoneal sarcomas [PDF]

open access: yesSurgical 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

Sarcoma retroperitoneal: relato de caso [PDF]

open access: yes, 2021
Introduction: Retroperitoneal sarcoma is a rare malignant tumor, originating in the mesenchymal cell that undergoes changes in its genetic code, thus producing atypical tissue.
de Oliveira, Diego Henrique   +4 more
core   +1 more source

Retroperitoneal Erdheim-Chester disease without skeletal bone involvement mimicking uterine sarcoma with multiple organ involvement [PDF]

open access: yesObstetrics & Gynecology Science, 2020
Erdheim-Chester disease (ECD) is a rare type of non-Langerhans cell histiocytosis and is characterized by the diffuse histiocytic infiltration of multiple organs. Retroperitoneal ECD, especially with uterine involvement, is extremely rare.
Hae Min Kim   +4 more
doaj   +1 more source

Late-onset meningeal metastases in liposarcoma: A case report and review of the literature [PDF]

open access: yes, 2006
Intracranial metastases from liposarcoma are rare and almost always preceded by the development of systemic tumour spread. We report here a case of liposarcoma with spread to the cranial nervous system 23 years after treatment of the primary tumour.
White, J.   +3 more
core   +1 more source

Actualización del manejo del sarcoma retroperitoneal [PDF]

open access: yes, 2020
Sarcomas represent a heterogeneous group of malignancies of mesenchymal origin that can arise from any anatomical site. Of soft tissue sarcomas, retroperitoneal sarcoma represents approximately 15-20%.
Jiménez Trigueros, José Pablo   +2 more
core   +1 more source

High grade sarcoma presenting as multifocal recurrent seromas after inguinal hernia repair: A case report

open access: yesRare Tumors, 2020
In this report, we describe a 54-year-old male with cystic retroperitoneal sarcoma extending through the inguinal canal. Patient initially underwent inguinal hernia repair with mesh placement for suspected cord lipoma, after which he developed recurrent ...
Lorne D Muir   +3 more
doaj   +1 more source

Blue Cell Tumour at Unusual Site: Retropritoneal Ewings Sarcoma [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
Ewing’s sarcoma is a highly malignant tumour of osseous or non-osseous origin, tremed as extra-skeletal Ewings sarcoma if arising from soft tissue. It is rare occurrence tumor most commonly occurring in paravertebral area, chest wall, head & neck and ...
Anita P Javalgi   +2 more
doaj   +1 more source

Ifosfamide with regional hyperthermia in soft-tissue sarcomas [PDF]

open access: yes, 2003
For high-risk soft tissue sarcomas (HR-STS) of adults, new treatment strategies are needed to improve outcome with regard to local control and overall survival.
M. Schlemmer   +5 more
core   +1 more source

The Role of Surgical Expertise and Surgical Access in Retroperitoneal Sarcoma Resection - A Retrospective Study. [PDF]

open access: yes, 2022
Background Retroperitoneal sarcoma (RPS) is a rare disease often requiring multi-visceral and wide margin resections for which a resection in a sarcoma center is advised. Midline incision seems to be the access of choice.
Beldi, G.   +9 more
core   +2 more sources

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