Manola Kalliopi N, Sambani Constantina, Karakasis Dimitris, Kalliakosta Georgia, Harhalakis Nicholas, Papaioannou Maria
Laboratory of Cytogenetics, National Center for Scientific Research (NCSR) "Demokritos", 15310 Aghia Paraskevi, Athens, Greece.
Leuk Res. 2008 Mar;32(3):481-6. doi: 10.1016/j.leukres.2007.06.004. Epub 2007 Jul 31.
Cases of leukemia associated with Turner syndrome (TS) are rare. Here we report three TS patients with leukemia including one case of T-large granular lymphocyte leukemia (T-LGL), one rare case of coexistence of chronic lymphocytic leukemia (CLL) and idiopathic myelofibrosis (IMF) and one case of a patient with AML-M2 who received autologous stem cell transplantation (SCT). T-LGL and coexistence of CLL and IMF associated with TS are reported for the first time while the last case represents the first report of SCT in a leukemia patient with TS. Our cases and the limited data of previously reported leukemia patients with TS suggest that TS is not associated with a specific type of leukemia and that presentation, clinical course and response to treatment are similar to that of the non-TS leukemia patients. However, these patients may have a higher risk of liver complications. Interestingly, in the mosaic TS patients, the abnormal clones were restricted to the monosomic 45,X cells, indicating that the leukemic clones possibly originate from the monosomic cell line. Even in cases with no additional chromosome abnormalities, the ratio of X/XX cells in bone marrow cells was significantly increased compared to that in constitutional karyotype, indicating that monosomic cells possibly provide a survival advantage for leukemia cells or that reduced programmed cell death may be responsible for the expansion of the monosomic cells.
与特纳综合征(TS)相关的白血病病例较为罕见。在此,我们报告3例患有白血病的TS患者,其中1例为T大颗粒淋巴细胞白血病(T-LGL),1例为罕见的慢性淋巴细胞白血病(CLL)与原发性骨髓纤维化(IMF)共存病例,还有1例急性髓系白血病M2(AML-M2)患者接受了自体干细胞移植(SCT)。T-LGL以及CLL与IMF共存并与TS相关的情况系首次报道,而最后1例则是白血病患者TS接受SCT的首例报道。我们的病例以及先前报道的白血病TS患者的有限数据表明,TS与特定类型的白血病无关,其临床表现、临床病程及对治疗的反应与非TS白血病患者相似。然而,这些患者可能有更高的肝脏并发症风险。有趣的是,在嵌合型TS患者中,异常克隆仅限于单体45,X细胞,这表明白血病克隆可能起源于单体细胞系。即使在无其他染色体异常的病例中,骨髓细胞中X/XX细胞的比例相较于核型分析中的比例也显著增加,这表明单体细胞可能为白血病细胞提供了生存优势,或者细胞程序性死亡减少可能是单体细胞扩增的原因。