Smadja N, Krulik M, Genot J Y, Audebert A A, Debray J
Cancer Genet Cytogenet. 1983 Jul;9(3):185-96. doi: 10.1016/0165-4608(83)90001-8.
The authors present two cases of patients with breast cancer with lymph node extension and who both had surgery. As a pancytopenia with hypercellular bone marrow was discovered at the same time in the first patient, she received no complementary treatment; 4 months later, she presented with an acute lymphocytic leukemia (ALL) for which a remission was easily induced, but she died of a pulmonary infection. The second patient received local radiotherapy (50 grays) and adjuvant chemotherapy (Alkeran for 26 months). Forty-seven months after the diagnosis of breast cancer and 16 months after the end of the treatment, an acute nonlymphoblastic leukemia (ANLL; M6) was diagnosed after 8 months of a preleukemic state. Treatment did not produce any results and death occurred on the 17th day. Cytogenetic studies on the bone marrow cells of both patients were performed. In the first patient in the ALL phase normal cells coexisted with a 47 chromosome clone, the extra chromosome being a D (+ 13?). In the second patient, several karyotype abnormalities were already present in the preleukemic state and also during the acute leukemic phase. No normal mitoses were found; hypodiploidy was present as well as major abnormalities such as markers, rings, and, among others, the systematic loss of a #5 and a #7. The first patient seems to have presented with a de novo ALL, associated with the malignant tumor; whereas, the second patient showed all the characteristics of an induced ANLL. The clinical, hematologic, and cytogenetic characteristics of these two patients are analyzed and compared to those of other cases in the literature.
作者报告了两例伴有淋巴结转移且均接受了手术的乳腺癌患者。首例患者同时被发现存在全血细胞减少伴骨髓细胞增多,因此未接受辅助治疗;4个月后,她发展为急性淋巴细胞白血病(ALL),该白血病很容易诱导缓解,但她最终死于肺部感染。第二例患者接受了局部放疗(50戈瑞)及辅助化疗(马法兰,共26个月)。在乳腺癌诊断47个月后以及治疗结束16个月后,该患者在经历了8个月的白血病前期状态后被诊断为急性非淋巴细胞白血病(ANLL;M6)。治疗未取得任何效果,患者在第17天死亡。对两名患者的骨髓细胞进行了细胞遗传学研究。首例处于ALL阶段的患者,正常细胞与一个47条染色体的克隆共存,额外的染色体为一条D染色体(+13?)。第二例患者在白血病前期状态以及急性白血病阶段均已出现几种核型异常。未发现正常有丝分裂;存在亚二倍体以及如标记染色体、环状染色体等主要异常,此外还存在5号和7号染色体的系统性缺失。首例患者似乎表现为与恶性肿瘤相关的原发性ALL;而第二例患者则表现出诱导性ANLL的所有特征。对这两名患者的临床、血液学及细胞遗传学特征进行了分析,并与文献中其他病例的特征进行了比较。