Esteve J, Cervantes F, Rives S, Rozman M, Zarco M A, Montserrat E
Department of Hematology and Postgraduate School of Hematology Farreras Valenti, University of Barcelona, Spain.
Haematologica. 1997 Sep-Oct;82(5):596-9.
The coexistence of chronic myeloid leukemia (CML) and B-cell chronic lymphocytic leukemia (CLL) in the same patient is rare. A 71-year-old woman developed a B-lineage lymphoid blast crisis at 18 months after diagnosis of Ph-positive CML. At this time, a lymphoid cell population with morphologic and immunophenotypic features of CLL was demonstrated. The retrospective review of the tests performed at diagnosis and thereafter disclosed the presence of lymphoid nodules in the initial bone marrow biopsy in the absence of lymphocytosis. Subsequently, there was an appearance of moderate lymphocytosis in the following months. Therefore, diagnosis of CML and coexistent CLL was established. Although a transient remission of blast crisis was achieved, blast cells reappeared two months later and the patient died shortly afterwards. Molecular studies of the immunoglobulin heavy chain gene (IH) rearrangement pattern point to the origin of the diseases in two different cell clones. In addition, previously published cases of simultaneous CLL and CML are reviewed.
慢性髓性白血病(CML)与B细胞慢性淋巴细胞白血病(CLL)在同一患者中共存的情况较为罕见。一名71岁女性在诊断为Ph阳性CML 18个月后发生了B系淋巴母细胞危象。此时,发现了具有CLL形态学和免疫表型特征的淋巴细胞群。对诊断时及之后所做检查的回顾性分析显示,初始骨髓活检时存在淋巴小结,但无淋巴细胞增多。随后,在接下来的几个月中出现了中度淋巴细胞增多。因此,确诊为CML合并CLL。尽管母细胞危象实现了短暂缓解,但两个月后母细胞再次出现,患者随后不久死亡。免疫球蛋白重链基因(IH)重排模式的分子研究表明,这两种疾病起源于两个不同的细胞克隆。此外,还对先前发表的CLL和CML同时存在的病例进行了综述。