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Pediatric Soft Tissue Sarcomas
Seminars in Ultrasound, CT and MRI, 2011After a brief discussion of the rarity of soft tissue sarcomas in children and of the limited ability of magnetic resonance imaging to provide a tissue diagnosis, this article discusses the incidence, presentation, treatment, prognosis, and imaging characteristics of the more common and unusual pediatric soft tissue sarcomas.
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2014
Sarcoma is a cancer that arises from cells of mesenchymal origin, such as bone, cartilage, muscle, fat, vascular, or hematopoietic tissue. It is a very rare form of cancer with over 50 histologic subtypes. This chapter discusses selected individual subtypes of sarcomas and characteristics specific to each one. It will broadly go over molecular biology,
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Sarcoma is a cancer that arises from cells of mesenchymal origin, such as bone, cartilage, muscle, fat, vascular, or hematopoietic tissue. It is a very rare form of cancer with over 50 histologic subtypes. This chapter discusses selected individual subtypes of sarcomas and characteristics specific to each one. It will broadly go over molecular biology,
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Orthopaedic Nursing, 2007
Malignancy of soft tissue, referred to as sarcomas, are some of the rarest tumors in medicine. These tumors account for approximately 1% of all diagnosed malignancies. Diagnosis of soft tissue sarcoma (STS) is a complex process that includes history and physical examination of patient, diagnostic imaging studies, and biopsy when indicated.
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Malignancy of soft tissue, referred to as sarcomas, are some of the rarest tumors in medicine. These tumors account for approximately 1% of all diagnosed malignancies. Diagnosis of soft tissue sarcoma (STS) is a complex process that includes history and physical examination of patient, diagnostic imaging studies, and biopsy when indicated.
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Primary Retroperitoneal Soft-Tissue Sarcomas
Journal of Urology, 1984AbstractOf the 98 soft‐tissue sarcomas treated between 1973–1978, 12 were retroperitoneal in origin. Fifty percent underwent one to three previous surgical procedures. All patients were operated on. In 75% (nine out of 12), the tumor was completely resected. The operative mortality for total tumor excision was 11%.
Y G, Adam, J, Oland, A, Halevy, R, Reif
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1995
In many ways the title “rare soft tissue sarcomas” is tautologous since, in relative terms, soft tissue sarcomas as a whole are comparatively uncommon. It is an interesting anomaly that the lesions to be covered in this chapter, while collectively accounting for only around 3%–4% of sarcomas and less than 0.04% of all malignancies, are, at least in ...
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In many ways the title “rare soft tissue sarcomas” is tautologous since, in relative terms, soft tissue sarcomas as a whole are comparatively uncommon. It is an interesting anomaly that the lesions to be covered in this chapter, while collectively accounting for only around 3%–4% of sarcomas and less than 0.04% of all malignancies, are, at least in ...
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1991
The advances made over the past two decades in multimodal treatment for soft parts sarcoma with increased disease-free survival are among the notables in oncology achievements. More precise identification of tumor types, with better understanding of their biological behavior and therapeutic sensitivities, and the advances in diagnostic technology for ...
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The advances made over the past two decades in multimodal treatment for soft parts sarcoma with increased disease-free survival are among the notables in oncology achievements. More precise identification of tumor types, with better understanding of their biological behavior and therapeutic sensitivities, and the advances in diagnostic technology for ...
openaire +2 more sources