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作 者:朱剑锋[1] 吴正东[1] 范磊[2] 徐卫[2] 李建勇[2]
机构地区:[1]南通大学附属泰州市人民医院血液科,江苏省泰州市225300 [2]南京医科大学第一附属医院、江苏省人民医院血液科,210029
出 处:《中华医学遗传学杂志》2016年第1期13-16,共4页Chinese Journal of Medical Genetics
摘 要:目的探讨7例不典型套细胞淋巴瘤(mantlecelllymphoma,MCL)的临床特点与诊断。方法对7例因免疫表型积分为4分而误诊为慢性淋巴细胞白血病(chroniclymphocyticleukemia,CLL)的MCL患者的临床特点和诊断进行回顾。结果7例患者中浅表淋巴结肿大但难以触及者6例。所有患者均因广泛浸润骨髓被分为Ⅳ期,CLL免疫表型积分为4分,间期荧光原位杂交检测t(11;14)均为阳性。结论部分MCI。患者临床表现与CLL相似,间期荧光原位杂交检查将有助于其诊断。Objective To study the clinical features and diagnosis of 7 patients with atypical mantle cell lymphoma (MCL) . Methods The 7 MCL patients were misdiagnosed as chronic lymphocytic leukemia (CLL) due to a score of 4 for their immunophenotypes. The clinical features and diagnosis of such patients were retrospectively analyzed. Results Six patients had superficial lymphadeneetasis but their lymph nodes could not be palpated. All 7 patients were as stage IV considering bone marrow infiltration. Scores of immunophenotype of CLL were 4, and interphase fluorescence in situ hybridization (FISH) for t(11;14) were positive in all patients. Conclusion Some MCL patients have clinicai features similar to CLL. Interphase FISH can play an important role in the diagnosis of MCL.
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