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一名慢性粒细胞白血病患者同时发生母细胞性套细胞淋巴瘤并文献复习

Blastic mantle cell lymphoma developing concurrently in a patient with chronic myelogenous leukemia and a review of the literature.

作者信息

Rodler Eve, Welborn Jeanna, Hatcher Sandra, Unger Katherine, Larkin Edward, Gumerlock Paul H, Wun Theodore, Richman Carol

机构信息

Division of Hematology/Oncology in the Department of Internal Medicine, University of California, Davis, California, USA.

出版信息

Am J Hematol. 2004 Apr;75(4):231-8. doi: 10.1002/ajh.20025.

Abstract

Non-Hodgkin's lymphoma (NHL) occurring as a synchronous malignancy with chronic myelogenous leukemia (CML) is rare. To our knowledge, this is the first case reported of a patient who developed mantle cell lymphoma (MCL) after therapy with imatinib mesylate for CML. After a 3-year history of CML, the patient developed a lymphocytosis associated with diarrhea, anorexia, and weight loss. Imaging studies revealed abdominal adenopathy and extensive lymphomatous infiltration of the liver, stomach, pancreas, and kidneys. Flow cytometric and cytogenetic studies were consistent with MCL. Fluorescence in situ hybridization (FISH) of the bone marrow revealed a genetically distinct lymphoid neoplasm rather than an extramedullary blast crisis of CML. The development of lung cancer, prostate cancer, CML and MCL in this patient suggests a genetic predisposition, although other factors, including environmental exposures and therapy with imatinib mesylate could have had a contributory or synergistic role in the development of MCL.

摘要

非霍奇金淋巴瘤(NHL)作为慢性粒细胞白血病(CML)的同步恶性肿瘤较为罕见。据我们所知,这是首例报告的在接受甲磺酸伊马替尼治疗CML后发生套细胞淋巴瘤(MCL)的患者。在CML病史3年后,该患者出现淋巴细胞增多,并伴有腹泻、厌食和体重减轻。影像学研究显示腹部淋巴结肿大以及肝脏、胃、胰腺和肾脏广泛的淋巴瘤浸润。流式细胞术和细胞遗传学研究结果与MCL相符。骨髓荧光原位杂交(FISH)显示为一种基因上不同的淋巴样肿瘤,而非CML的髓外原始细胞危象。该患者同时发生肺癌、前列腺癌、CML和MCL提示存在遗传易感性,尽管其他因素,包括环境暴露和甲磺酸伊马替尼治疗可能在MCL的发生中起到了促成或协同作用。

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