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.
出处
《中华医学遗传学杂志》
CAS
CSCD
北大核心
2016年第1期13-16,共4页
Chinese Journal of Medical Genetics