[Clinical Features and Prognosis of Primary Tonsil Lymphoma].

Q4 Medicine
Dan Luo, Qi-Miao Shan, Hua Ding, Jiao Liu, Zi-Qing Huang, Feng Zhu
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引用次数: 0

Abstract

Objective: To investigate the clinical features and prognostic factors of primary tonsil lymphoma (PTL).

Methods: The clinical data of 41 patients diagnosed with PTL and treated in the Affiliated Hospital of Xuzhou Medical University from January 2015 to December 2022 were collected and retrospectively analyzed. Their clinical features and prognostic factors were analyzed.

Results: All the 41 patients were newly diagnosed with PTL, and the median age of onset was 58(19-85) years. Among them, 19 patients started with pharyngeal pain, 12 patients presented with dysphagia, 8 patients presented with pharyngeal mass, and 2 patients presented with blurred articulation. The most common pathological type was diffuse large B-cell lymphoma (24 cases, 58.54%). All patients received chemotherapy, and 3 patients were combined with hematopoietic stem cell transplantation. Among 41 patients, 11 (26.83%) achieved complete response, 14 (34.15%) achieved partial response, and the total response rate was 60.98% (25/41). The median follow-up time was 37(6-107) months, the 5-year overall survival (OS) rate was 70.81% and 5-year progression-free survival (PFS) rate was 66.20%. Univariate analysis showed that B symptoms, Ki-67, β2-MG and IPI score had significant effects on PFS and OS of patients (all P < 0.05). Multivariate analysis showed that IPI score was an independent risk factor for PFS and OS of patients (P < 0.05).

Conclusion: The clinical manifestations of PTL lack specificity, and the prognosis is relatively good. Most patients can achieve long-term survival after treatment. IPI score is related to the prognosis.

原发性扁桃体淋巴瘤的临床特点及预后
目的:探讨原发性扁桃体淋巴瘤(PTL)的临床特点及预后因素。方法:收集2015年1月至2022年12月在徐州医科大学附属医院诊治的41例PTL患者的临床资料进行回顾性分析。分析其临床特点及预后因素。结果:41例患者均为新发PTL,中位发病年龄为58(19-85)岁。其中以咽部疼痛首发19例,以吞咽困难首发12例,以咽部肿块首发8例,以发音模糊首发2例。最常见的病理类型为弥漫性大b细胞淋巴瘤(24例,58.54%)。所有患者均接受化疗,其中3例合并造血干细胞移植。41例患者中,完全缓解11例(26.83%),部分缓解14例(34.15%),总缓解率60.98%(25/41)。中位随访时间37(6-107)个月,5年总生存率(OS)为70.81%,5年无进展生存率(PFS)为66.20%。单因素分析显示,B症状、Ki-67、β2-MG和IPI评分对患者PFS和OS有显著影响(均P < 0.05)。多因素分析显示IPI评分是患者PFS和OS的独立危险因素(P < 0.05)。结论:PTL临床表现缺乏特异性,预后较好。多数患者经治疗后可长期生存。IPI评分与预后相关。
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来源期刊
中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
7331
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