Jacobson S A
Cancer. 1977 Nov;40(5):2116-30. doi: 10.1002/1097-0142(197711)40:5<2116::aid-cncr2820400522>3.0.co;2-l.
Polyhistioma, a neoplasm whose basic cells are small and round like those of Ewing's sarcoma, but which differentiate into various mesenchymal structures, most often bone, is described. Those cases that produce cartilage have been called mesenchymal chondrosarcoma; the others therefore are mostly urecognized. The name "polyhistioma" is suggested in the hope that with this terminology more of these tumors will be diagnosed. Polyhistiomas are not excessively rare; they affect bone and soft tissue. Half the patients with polyhistiomas died within 2 years. Treatment has resulted in survival of over 20 years. Thirty-eight of the 144 patients with polyhistioma have survived 5 years or more following first definitive treatment. Thirty-seven cases of the disease are presented.
多组织细胞瘤是一种肿瘤,其基本细胞小而圆,类似于尤因肉瘤的细胞,但能分化为各种间充质结构,最常见的是骨组织。那些产生软骨的病例被称为间叶性软骨肉瘤;因此,其他病例大多未被认识。建议使用“多组织细胞瘤”这个名称,希望通过这个术语能诊断出更多此类肿瘤。多组织细胞瘤并非极为罕见;它们可累及骨骼和软组织。多组织细胞瘤患者中有一半在2年内死亡。治疗已使患者存活超过20年。144例多组织细胞瘤患者中有38例在首次确定性治疗后存活了5年或更长时间。本文展示了37例该疾病病例。