Echo A2 Methode De Francais PORTABLE

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Echo A2 Methode De Francais

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Soft tissue sarcomas (STS) in children and adolescents constitute a rare malignancy with a wide range of histologic subtypes and morphologic variants. Despite advances in the outcome of adult STS patients, there are only limited data on the treatment of patients with these tumors in childhood and adolescence. Common histologic subtypes in children are low-grade and high-grade sarcomas. In contrast to these subtypes, high-grade neuroendocrine sarcomas in pediatric patients occur very rarely. As for other STS, the role of surgery remains important in achieving local tumor control; however, new concepts have evolved in the treatment of high-grade malignancies. Prognostic parameters in pediatric STS are of special interest due to their effect on the decision to undertake potentially toxic adjuvant and maintenance chemotherapy, radiotherapy, and stem cell transplantation. The current review summarizes current treatment approaches for STS in childhood and adolescence, and emphasizes oncologic outcome, prognostic factors, and available options for combination therapy in this rare tumor entity.Insulin receptors on normal and malignant human epithelial cells.
Radioiodinated insulin and chloroiodo derivative bound avidly and specifically to a 180,000 daltons cell surface receptor in B5, CHOK1, and TTCC1 cells. Normal mammary epithelial cells and breast cancer cells, obtained from different patients, had no detectable receptor activity, suggesting that these cells do not have the normal target cell

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