Thirteen histologically verified cases of synovial sarcoma are described. Eight of them were followed for over five years. The commonest site of the tumour was in the lower limbs. The most frequent therapeutic measure was radical excision of the tumour and postoperative radiotherapy in daily fractions, total c. 5,500–7,000 r. The five-year survival rate was 5/8 (= 62.5%).
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