Piéron R, Wolff M, Meyniel D
Sem Hop. 1982 Apr 29;58(17):1031-4.
A case of primary reticulum-cell sarcoma of the rib is reported. This rare tumor arose in an unusual site and was revealed by an exceptional clinical picture. Extensive hemothorax was the initial manifestation. Follow-up exceeds five years. Prognosis is not as poor for reticulum-cell sarcoma as for Ewing sarcoma. After radical surgery, radiation therapy and chemotherapy, the five-year total remission rate approximates 50%.
报告了一例肋骨原发性网状细胞肉瘤。这种罕见肿瘤发生于不寻常部位，具有特殊的临床表现。广泛血胸是其首发表现。随访超过五年。网状细胞肉瘤的预后不像尤因肉瘤那样差。根治性手术、放疗和化疗后，五年总缓解率约为50%。
