Gottardi Michele, Gattei Valter, Degan Massimo, Bomben Riccardo, Zucchetto Antonella, Tecchio Cristina, Laurino Licia, Zanatta Lucia, Dei Tos Angelo Paolo, Mordacchini Maurizio, Canal Fabio, Gherlinzoni Filippo
Division of Hematology, Ca' Foncello Hospital, Treviso, Italy.
Leuk Lymphoma. 2006 May;47(5):885-9. doi: 10.1080/10428190500404761.
The simultaneous appearance of chronic lymphocytic leukemia (CLL) and acute myeloid leukemia (AML) has been rarely reported, with AML occurring more frequently as a secondary event in patients receiving cytotoxic drugs for a primary lymphoproliferative disorder. We describe a case of simultaneous CLL and AML documented by morphological and cytometric analysis in a previously untreated patient. In particular, on the basis of morphological and immunological features, the patient was diagnosed as being affected by CD34 + /CD13 + /CD33 + /HLA-DR + /CD7 + FAB-M2 AML, along with a B-CLL characterized by neoplastic cells expressing a VH3-53/D3-22/JH4 Ig, bearing, on average, 3.9% IgVH mutations without evidence of antigen-driven selection. To establish whether the two neoplastic cell populations shared some common molecular signature, we performed IgH gene rearrangement studies on CD34 + /CD19- and CD34-/CD19 + immunomagnetically sorted cell populations: only genomic DNA from the CD19 + /CD34- cell fraction revealed the presence of the IgH gene rearrangement. These results provide evidence that the rare concomitant association of CLL and AML likely arises from simultaneous expansion of two independent clones.
慢性淋巴细胞白血病(CLL)和急性髓系白血病(AML)同时出现的情况鲜有报道,在因原发性淋巴细胞增殖性疾病接受细胞毒性药物治疗的患者中,AML作为继发事件更为常见。我们描述了一例在一名未经治疗的患者中通过形态学和细胞计量分析确诊的CLL和AML同时发生的病例。具体而言,根据形态学和免疫学特征,该患者被诊断为患有CD34 + /CD13 + /CD33 + /HLA-DR + /CD7 + FAB-M2 AML,同时患有B-CLL,其特征为肿瘤细胞表达VH3-53/D3-22/JH4 Ig,平均携带3.9%的IgVH突变,且无抗原驱动选择的证据。为确定这两个肿瘤细胞群体是否共享某些共同的分子特征,我们对经免疫磁珠分选的CD34 + /CD19-和CD34-/CD19 +细胞群体进行了IgH基因重排研究:只有来自CD19 + /CD34-细胞组分的基因组DNA显示存在IgH基因重排。这些结果表明,CLL和AML罕见的伴随关联可能源于两个独立克隆的同时扩增。