结外自然杀伤/ t细胞淋巴瘤长期生存和反复复发:是否表明存在惰性亚型?

The Korean Journal of Hematology Pub Date : 2012-09-01 Epub Date: 2012-09-25 DOI:10.5045/kjh.2012.47.3.202
Seok Jin Kim, Yong Park, Byung Soo Kim, Insun Kim, Young Hye Ko, Won Seog Kim
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引用次数: 11

摘要

背景:结外自然杀伤细胞(NK)/ t细胞淋巴瘤是一种来源于NK细胞的淋巴瘤亚型。它被认为是一种侵袭性的非霍奇金淋巴瘤,因为经常复发和抵抗治疗。复发的NK/ t细胞淋巴瘤常伴有暴发性病程,对常规化疗难以治疗。方法:几例结外NK/ t细胞淋巴瘤患者虽然经常复发,但长期生存。因此,我们对1995年至2007年诊断为结外NK/ t细胞淋巴瘤的患者的医疗记录进行了回顾和评估。结果:140例病例中,入选6例(4.29%)。这些患者在随访期间至少有3次复发或疾病进展,他们的中位总生存期为66个月(范围42-89个月)。根据观察到的不典型临床行为进行分组:(1)随访期间反复复发或进展(≥3次);(2)长期生存期超过40个月,因为之前认为最长的总生存中值约为40个月。这些患者的临床病理和实验室特征与其他结外NK/ t细胞淋巴瘤患者相似。然而,5例研究病例涉及相对较低的增殖相关抗原Ki-67表达(结论:我们的观察表明,一些结外NK/ t细胞淋巴瘤患者的临床行为不同于典型的临床病程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Extranodal natural killer/T-cell lymphoma with long-term survival and repeated relapses: does it indicate the presence of indolent subtype?

Extranodal natural killer/T-cell lymphoma with long-term survival and repeated relapses: does it indicate the presence of indolent subtype?

Extranodal natural killer/T-cell lymphoma with long-term survival and repeated relapses: does it indicate the presence of indolent subtype?

Background: Extranodal natural killer (NK)/T-cell lymphoma is a subtype of lymphoma that is derived from NK cells. It is considered as an aggressive form of non-Hodgkin's lymphoma because of frequent relapses and resistance to treatment. Relapsed NK/T-cell lymphoma often follows a fulminant course that is refractory to conventional chemotherapy treatment.

Methods: Several patients with extranodal NK/T-cell lymphoma showed long-term survival in spite of frequent relapses. Thus, the medical records of patients diagnosed with extranodal NK/T-cell lymphoma from 1995 to 2007 were reviewed and assessed.

Results: Of the 140 cases reviewed, 6 were selected (4.29%). Each of these patients had a minimum of 3 relapses or disease progression during the follow-up period, and their median overall survival was 66 months (range, 42-89 months). They were grouped according to the atypical clinical behavior observed: (1) repeated relapses or progression (≥3 times) during follow-up; and (2) long-term survival of more than 40 months, as the longest overall survival median was previously considered at approximately 40 months. The clinicopathological and laboratory characteristics of these patients were similar to those of other extranodal NK/T-cell lymphoma patients. However, 5 of the studied cases involved relatively lower expression of the proliferation-related antigen Ki-67 (<40-50%), indicating less proliferative activity. Clinically, they showed delayed relapse for at least 20 months after the initial complete remission.

Conclusion: Our observations suggest that the clinical behavior of some extranodal NK/T-cell lymphoma patients differs from the typical clinical course.

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