[Clinical Characteristics and Prognosis of Primary Pulmonary Lymphoma].

Q4 Medicine
You-Fan Feng, Yuan-Yuan Zhang, Xiao Fang Wei, Qi-Ke Zhang, Li Zhao, Xiao-Qin Liang, Yuan Fu, Fei Liu, Yang-Yang Zhao, Xiu-Juan Huang, Qing-Fen Li
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引用次数: 0

Abstract

Objective: To investigate the clinical characteristics and prognosis of primary pulmonary lymphoma (PPL).

Methods: The clinical data of 17 patients with PPL admitted to Gansu Provincial Hospital from January 2013 to June 2023 were collected, and their clinical characteristics and prognosis were retrospectively analyzed and summarized.

Results: The median age of the 17 patients was 56 (29-73) years old. There were 8 males and 9 females. According to Ann Arbor staging system, there were 9 patients with stage I-II and 8 patients with stage III-IV. There were 14 patients with IPI score of 0-2 and 3 patients with IPI score of 3-4. All 17 patients had symptoms at the initial diagnosis, most of the first symptoms were cough, and 6 patients had B symptoms.Among the 17 patients, there were 8 cases of diffuse large B-cell lymphoma (DLBCL), 5 cases of mucosa-associated lymphoid tissue (MALT) lymphoma, 1 case of gray zone lymphoma (GZL), and 3 cases of Hodgkin's lymphoma (HL). 15 patients received chemotherapy, of which 3 cases received autologous hematopoietic stem cell transplantation(ASCT) and 3 cases received radiotherapy; 2 patients did not receive treatment. The median number of chemotherapy courses was 6(2-8). The short-term efficacy was evaluated, 12 patients achieved complete remission (CR) and 3 patients achieved partial remission (PR). The age, pathological subtype, sex, Ann Arbor stage, β2-microglobulin(β2-MG) level, lactate dehydrogenase(LDH) level were not correlated with CR rate (P >0.05), while IPI score was correlated with recent CR rate (P < 0.05 ). The median follow-up time was 31(2-102) months. One of the 12 CR patients died of COVID-19, and the rest survived. Among the 3 patients who did not reach CR, 1 died after disease progression, while the other 2 survived. One of the 2 untreated patients died one year after diagnosis. Both the median progression-free survival (PFS) time and overall survival (OS) time of the 17 patients were both 31 (2-102) months.

Conclusion: The incidence of PPL is low, and the disease has no specific clinical manifestations, which is easily missed and misdiagnosed. The pathological subtypes are mainly MALT lymphoma and DLBCL, and the treatment is mainly combined chemotherapy. The IPI score is related to the treatment efficacy.

原发性肺淋巴瘤的临床特点及预后
目的:探讨原发性肺淋巴瘤(PPL)的临床特点及预后。方法:收集2013年1月至2023年6月甘肃省立医院收治的17例PPL患者的临床资料,对其临床特点及预后进行回顾性分析和总结。结果:17例患者中位年龄为56岁(29 ~ 73岁)。其中男性8人,女性9人。根据Ann Arbor分期系统,I-II期9例,III-IV期8例。IPI评分0-2分的患者14例,IPI评分3-4分的患者3例。17例患者初诊均有症状,首发症状多为咳嗽,6例为B型症状。17例患者中弥漫性大b细胞淋巴瘤(DLBCL) 8例,粘膜相关淋巴组织淋巴瘤(MALT) 5例,灰色地带淋巴瘤(GZL) 1例,霍奇金淋巴瘤(HL) 3例。化疗15例,其中自体造血干细胞移植(ASCT) 3例,放疗3例;2例患者未接受治疗。化疗疗程中位数为6(2-8)。评估短期疗效,12例患者达到完全缓解(CR), 3例患者达到部分缓解(PR)。年龄、病理亚型、性别、Ann Arbor分期、β2-微球蛋白(β2-MG)水平、乳酸脱氢酶(LDH)水平与CR率无相关性(P < 0.05),而IPI评分与近期CR率相关(P < 0.05)。中位随访时间为31(2-102)个月。12例CR患者中有1例死于COVID-19,其余患者存活。未达到CR的3例患者中,1例因病情进展死亡,2例存活。2例未经治疗的患者中有1例在诊断一年后死亡。17例患者的中位无进展生存期(PFS)和总生存期(OS)均为31(2-102)个月。结论:PPL发病率低,无特异性临床表现,易漏诊和误诊。病理亚型以MALT淋巴瘤和DLBCL为主,治疗以联合化疗为主。IPI评分与治疗效果相关。
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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
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0.00%
发文量
7331
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