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伊马替尼治疗的慢性髓性白血病患者中伴有11q22.3重排的B细胞慢性淋巴细胞白血病

B-Cell Chronic Lymphocytic Leukemia with 11q22.3 Rearrangement in Patient with Chronic Myeloid Leukemia Treated with Imatinib.

作者信息

Lewandowski Krzysztof, Gniot Michał, Lewandowska Maria, Wache Anna, Ratajczak Błażej, Czyż Anna, Jarmuż-Szymczak Małgorzata, Komarnicki Mieczysław

机构信息

Department of Hematology and Stem Cell Transplantation, Poznan University of Medical Sciences, Szamarzewskiego 82/84, 60-569 Poznan, Poland.

Department of Hematology and Stem Cell Transplantation, Poznan University of Medical Sciences, Szamarzewskiego 82/84, 60-569 Poznan, Poland; Institute of Human Genetics, Polish Academy of Sciences, Strzeszyńska 32, 60-479 Poznan, Poland.

出版信息

Case Rep Med. 2016;2016:9806515. doi: 10.1155/2016/9806515. Epub 2016 Mar 3.

Abstract

The coexistence of two diseases chronic myeloid leukemia (CML) and B-cell chronic lymphocytic leukemia (B-CLL) is a rare phenomenon. Both neoplastic disorders have several common epidemiological denominators (they occur more often in men over 50 years of age) but different origin and long term prognosis. In this paper we described the clinical and pathological findings in patient with CML in major molecular response who developed B-CLL with 11q22.3 rearrangement and Coombs positive hemolytic anemia during the imatinib treatment. Due to the presence of the symptoms of autoimmune hemolytic anemia and optimal CML response to the imatinib treatment, the decision about combined therapy with prednisone and imatinib was made. During the follow-up, the normalization of complete blood count and resolution of peripheral lymphadenopathy were noted. The hematologic response of B-CLL was diagnosed. The repeated FISH analysis of cultured peripheral blood lymphocytes showed 2% of cells carrying 11q22.3 rearrangement. At the same time, molecular monitoring confirmed the deep molecular response of CML. The effectiveness of such combination in the described case raises the question about the best therapeutic option in such situation, especially in patients with good imatinib tolerance and optimal response.

摘要

慢性粒细胞白血病(CML)和B细胞慢性淋巴细胞白血病(B-CLL)这两种疾病并存是一种罕见现象。这两种肿瘤性疾病有几个共同的流行病学特征(它们在50岁以上男性中更常见),但起源和长期预后不同。在本文中,我们描述了一名处于主要分子反应阶段的CML患者的临床和病理表现,该患者在伊马替尼治疗期间发生了伴有11q22.3重排的B-CLL以及Coombs阳性溶血性贫血。由于存在自身免疫性溶血性贫血症状且CML对伊马替尼治疗反应良好,因此决定采用泼尼松和伊马替尼联合治疗。在随访期间,全血细胞计数恢复正常,外周淋巴结病消退。诊断出B-CLL的血液学反应。对培养的外周血淋巴细胞进行的重复荧光原位杂交(FISH)分析显示,2%的细胞携带11q22.3重排。与此同时,分子监测证实了CML的深度分子反应。上述病例中这种联合治疗的有效性引发了关于这种情况下最佳治疗选择的问题,特别是对于伊马替尼耐受性良好且反应最佳的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82ec/4807041/5bf76c946e54/CRIM2016-9806515.001.jpg

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