Hecht T, Henke M, Schempp W, Bross K J, Löhr G W
Medizinische Universitätsklinik Freiburg, Abteilung für Hämatologie und Onkologie, Federal Republic of Germany.
Blut. 1988 Jun;56(6):261-4. doi: 10.1007/BF00320286.
The development of acute lymphoblastic leukemia (c-ALL) in identical twins is reported. The first born had ALL in 1982 and bone marrow transplantation was performed in first complete remission (CR) from his healthy twin-brother the same year. The bone marrow donor developed ALL in 1985; he received an autologous bone marrow transplantation in first CR in 1986. Unfortunately, both patients relapsed in 1986. Cytogenetic studies of the first born revealed multiple chromosomal abnormalities and a marker chromosome whereas the second patient had a Philadelphia chromosome. Genetic reasons or exposure to leukemogenic agents may be responsible for the onset of these leukemias.
据报道,一对同卵双胞胎均患急性淋巴细胞白血病(c-ALL)。老大于1982年患ALL,并于同年在首次完全缓解期(CR)接受了来自其健康双胞胎兄弟的骨髓移植。骨髓供者于1985年患ALL;他于1986年在首次CR时接受了自体骨髓移植。不幸的是,两名患者均于1986年复发。对老大的细胞遗传学研究显示有多种染色体异常及一条标记染色体,而第二名患者有一条费城染色体。遗传因素或接触致白血病因子可能是这些白血病发病的原因。