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Ca-A Cancer Journal for Clinicians, 1978 Some of the next articles are maybe not open access.
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Surgical Clinics of North America, 2000
Sarcomas of the soft tissues are challenging lesions for the surgical oncologist. Careful planning must be done at all stages of diagnosis and treatment, because every sarcoma is unique with respect to histologic type, size, and location. Pretreatment discussions in a multidisciplinary format are useful to ensure appropriate and effective management of
J F, Moley, T J, Eberlein
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Sarcomas of the soft tissues are challenging lesions for the surgical oncologist. Careful planning must be done at all stages of diagnosis and treatment, because every sarcoma is unique with respect to histologic type, size, and location. Pretreatment discussions in a multidisciplinary format are useful to ensure appropriate and effective management of
J F, Moley, T J, Eberlein
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Seminars in Ultrasound, CT and MRI, 2021
Imaging evaluation of soft tissue masses is essential for diagnosis, preoperative staging, and post-treatment follow-up. Magnetic resonance imaging plays the major role because of its superior resolution that helps in better tissue characterization, and its multiplanar imaging capability in evaluation of soft tissue masses.
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Imaging evaluation of soft tissue masses is essential for diagnosis, preoperative staging, and post-treatment follow-up. Magnetic resonance imaging plays the major role because of its superior resolution that helps in better tissue characterization, and its multiplanar imaging capability in evaluation of soft tissue masses.
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Cancer, 2007
Sarcomas have been diagnosed from ancient times, but the term sarcoma was used for benign as well as malignant tumors until the middle 1800s. The treatment for soft tissue sarcomas was surgery for 2000 years. In the 1970s, multimodality therapy and the TNM system for staging were introduced.
Albritton k, Ferrari A, Casanova M
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Sarcomas have been diagnosed from ancient times, but the term sarcoma was used for benign as well as malignant tumors until the middle 1800s. The treatment for soft tissue sarcomas was surgery for 2000 years. In the 1970s, multimodality therapy and the TNM system for staging were introduced.
Albritton k, Ferrari A, Casanova M
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Journal of the American Academy of Orthopaedic Surgeons, 2009
Soft-tissue sarcomas are rare malignancies of mesodermal origin. Common sites of involvement include the extremities, trunk, retroperitoneum, and the head and neck. Soft-tissue sarcomas of the extremities and pelvis are the most relevant to the orthopaedic surgeon.
Nathan F, Gilbert +3 more
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Soft-tissue sarcomas are rare malignancies of mesodermal origin. Common sites of involvement include the extremities, trunk, retroperitoneum, and the head and neck. Soft-tissue sarcomas of the extremities and pelvis are the most relevant to the orthopaedic surgeon.
Nathan F, Gilbert +3 more
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Current Problems in Surgery, 1989
Soft tissue sarcomas in infants and children differ from those in adults in clinical presentation, histology, and response to therapy. For rhabdomyosarcoma, the most common sarcoma in children, each primary site has special characteristics that affect both treatment programs and survival rates.
W, Lawrence, J P, Neifeld
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Soft tissue sarcomas in infants and children differ from those in adults in clinical presentation, histology, and response to therapy. For rhabdomyosarcoma, the most common sarcoma in children, each primary site has special characteristics that affect both treatment programs and survival rates.
W, Lawrence, J P, Neifeld
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2013
Soft tissue sarcomas are a heterogeneous group of non-epithelial extraskeletal malignancies accounting for about 8 % of childhood cancers. Half of the cases are represented by rhabdomyosarcoma, a typical embryonal tumor of childhood, characterized by high grade of malignancy and strong propensity to metastasize, but also by a general good response to ...
Sultan I, Ortiz R, Ferrari A
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Soft tissue sarcomas are a heterogeneous group of non-epithelial extraskeletal malignancies accounting for about 8 % of childhood cancers. Half of the cases are represented by rhabdomyosarcoma, a typical embryonal tumor of childhood, characterized by high grade of malignancy and strong propensity to metastasize, but also by a general good response to ...
Sultan I, Ortiz R, Ferrari A
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Soft-tissue sarcomas: an update
European Journal of Surgical Oncology (EJSO), 1999Despite their relative infrequency (which is often used as an excuse for poor treatment), soft-tissue sarcomas have been the focus of considerable interest and advances in recent years, mainly because of molecular genetic developments as well as evolution in their histological classification.
De Saint Aubain, Nicolas +1 more
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Clinical Oncology, 1992
Soft tissue sarcomas are rare, with some 1200 new cases in the UK each year; clinicians outside specialist centres see no more than a few. They involve principally the soft connective tissues of the limbs, limb girdles and retroperitoneum, and also occur in the head and neck, and abdominal and chest walls.
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Soft tissue sarcomas are rare, with some 1200 new cases in the UK each year; clinicians outside specialist centres see no more than a few. They involve principally the soft connective tissues of the limbs, limb girdles and retroperitoneum, and also occur in the head and neck, and abdominal and chest walls.
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Current Opinion in Oncology, 1999
Soft tissue sarcomas are a heterogeneous group of tumors, consisting of numerous histiotypes that all share a putative common mesenchymal origin. Although prognosis of these tumors is determined by clinical parameters (size, location, and resection margin status) and pathologic features (mitotic activity and necrosis), the histologic subtype has never ...
Dirix, L.Y., van Oosterom, A.T.
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Soft tissue sarcomas are a heterogeneous group of tumors, consisting of numerous histiotypes that all share a putative common mesenchymal origin. Although prognosis of these tumors is determined by clinical parameters (size, location, and resection margin status) and pathologic features (mitotic activity and necrosis), the histologic subtype has never ...
Dirix, L.Y., van Oosterom, A.T.
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