Mathé G, Pouillart P, Schwarzenberg L, Hayat M, Amiel J L, Schlumberger J R, Misset J, Musset M, Jasmin C, De Vassal F
Br J Cancer Suppl. 1975 Mar;2:96-101.
In 143 patients with poorly differentiated lymphosarcoma, leukaemic conversion has been observed in 25. The cytological type was prolymphocytic or lymphoblastic or lymphoblastoid (immunoblastic ?). Twenty-five patients were treated with chemo-radiotherapy, followed by active immunotherapy as if they had primary acute lymphoid leukaemia. A complete remission was obtained in 11. Four are still in first complete remission after 4 1/2 years. Among 136 patients suffering from so-called "poorly differentiated reticulosarcoma", 17 became leukaemic. The cells are cytologically very dystrophic and unidentifiable. A remission was obtained in 7 patients but it was of short duration (median 1 1/2 months, longest 7 months).
在143例低分化淋巴肉瘤患者中,观察到25例发生白血病转化。细胞类型为原淋巴细胞性、淋巴母细胞性或淋巴母细胞样(免疫母细胞性?)。25例患者接受了化疗放疗,随后进行主动免疫治疗,就好像他们患有原发性急性淋巴细胞白血病一样。11例获得完全缓解。4例在4年半后仍处于首次完全缓解状态。在136例所谓的“低分化网状细胞肉瘤”患者中,17例发生白血病。细胞在细胞学上非常营养不良且无法识别。7例患者获得缓解,但持续时间较短(中位时间为1个半月,最长为7个月)。