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原发与继发甲状腺淋巴瘤的临床特征和预后比较
OBJECTIVE: To compare clinical characteristics and prognosis between patients with primary (PTL) and secondary thyroid lymphoma (STL). METHODS: A retrospective analysis was performed on 46 patients with thyroid lymphoma (PTL 19, STL 27) from January 2002 to October 2018. RESULTS: ①PTL group included...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
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Editorial office of Chinese Journal of Hematology
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364891/ https://www.ncbi.nlm.nih.gov/pubmed/32397019 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.07.006 |
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collection | PubMed |
description | OBJECTIVE: To compare clinical characteristics and prognosis between patients with primary (PTL) and secondary thyroid lymphoma (STL). METHODS: A retrospective analysis was performed on 46 patients with thyroid lymphoma (PTL 19, STL 27) from January 2002 to October 2018. RESULTS: ①PTL group included 4 males and 15 females, with a median age of 57 years. The STL group included 10 males and 17 females, with a median age of 61 years. Diffuse large B-cell lymphoma (DLBCL) was the main pathological subtype in both PTL and STL groups, with 14 cases (73.7%) and 20 cases (74.1%) respectively. In terms of clinical manifestations, goiter was the most common symptom in PTL patients 100.0% (19/19), while 29.6% (8/27) STL had goiter (P<0.001). The incidences of increased thyroglobulin antibody (TRAb) /thyroid peroxidase antibody (TPO) were 81.3% (13/16) in PTL group and 43.8% (7/16) in STL group (P=0.028) respectively. Concerning the clinical features of patients, only two PTL patients (10.5%) with advanced Ann Arbor stage (Ⅲ/Ⅳ), while 21 (77.8%) STL experienced advanced Ann Arbor stage (P<0.001). Elevated serum β(2)-MG were appeared in 1 (7.1%) PTL and 9 (47.4%) STL patients (P=0.013), and advanced IPI score (3-5) was more common in STL than PTL (59.3% vs 5.3%, P<0.001). ②Among the 17 PTL patients who received treatments, 15 (88.2%) achieved remission; as for STL patients received treatments, 23/25 (92.0%) were in remission. The 5-year overall survival (OS) rates of PTL (n=17) and STL groups (n=25) were (87.4±8.4) % and (70.0±13.1) % (P=0.433) respectively. ③The 5-year OS rate in 41 patients with B-cell thyroid lymphoma was (81.1±7.5) %. Univariate analysis showed that IPI score of 3-5 (P=0.040) and high level of serum IL-8 (P=0.022) were significantly associated with poor outcome. CONCLUSION: DLBCL was the most common subtype in both PTL and STL, and goiter was the major symptom in PTL. IPI score of 3-5 and high level of serum IL-8 were unfavorable prognostic factors for patients with B-cell thyroid lymphoma. |
format | Online Article Text |
id | pubmed-7364891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Editorial office of Chinese Journal of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73648912020-07-16 原发与继发甲状腺淋巴瘤的临床特征和预后比较 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To compare clinical characteristics and prognosis between patients with primary (PTL) and secondary thyroid lymphoma (STL). METHODS: A retrospective analysis was performed on 46 patients with thyroid lymphoma (PTL 19, STL 27) from January 2002 to October 2018. RESULTS: ①PTL group included 4 males and 15 females, with a median age of 57 years. The STL group included 10 males and 17 females, with a median age of 61 years. Diffuse large B-cell lymphoma (DLBCL) was the main pathological subtype in both PTL and STL groups, with 14 cases (73.7%) and 20 cases (74.1%) respectively. In terms of clinical manifestations, goiter was the most common symptom in PTL patients 100.0% (19/19), while 29.6% (8/27) STL had goiter (P<0.001). The incidences of increased thyroglobulin antibody (TRAb) /thyroid peroxidase antibody (TPO) were 81.3% (13/16) in PTL group and 43.8% (7/16) in STL group (P=0.028) respectively. Concerning the clinical features of patients, only two PTL patients (10.5%) with advanced Ann Arbor stage (Ⅲ/Ⅳ), while 21 (77.8%) STL experienced advanced Ann Arbor stage (P<0.001). Elevated serum β(2)-MG were appeared in 1 (7.1%) PTL and 9 (47.4%) STL patients (P=0.013), and advanced IPI score (3-5) was more common in STL than PTL (59.3% vs 5.3%, P<0.001). ②Among the 17 PTL patients who received treatments, 15 (88.2%) achieved remission; as for STL patients received treatments, 23/25 (92.0%) were in remission. The 5-year overall survival (OS) rates of PTL (n=17) and STL groups (n=25) were (87.4±8.4) % and (70.0±13.1) % (P=0.433) respectively. ③The 5-year OS rate in 41 patients with B-cell thyroid lymphoma was (81.1±7.5) %. Univariate analysis showed that IPI score of 3-5 (P=0.040) and high level of serum IL-8 (P=0.022) were significantly associated with poor outcome. CONCLUSION: DLBCL was the most common subtype in both PTL and STL, and goiter was the major symptom in PTL. IPI score of 3-5 and high level of serum IL-8 were unfavorable prognostic factors for patients with B-cell thyroid lymphoma. Editorial office of Chinese Journal of Hematology 2019-07 /pmc/articles/PMC7364891/ /pubmed/32397019 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.07.006 Text en 2019年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal. |
spellingShingle | 论著 原发与继发甲状腺淋巴瘤的临床特征和预后比较 |
title | 原发与继发甲状腺淋巴瘤的临床特征和预后比较 |
title_full | 原发与继发甲状腺淋巴瘤的临床特征和预后比较 |
title_fullStr | 原发与继发甲状腺淋巴瘤的临床特征和预后比较 |
title_full_unstemmed | 原发与继发甲状腺淋巴瘤的临床特征和预后比较 |
title_short | 原发与继发甲状腺淋巴瘤的临床特征和预后比较 |
title_sort | 原发与继发甲状腺淋巴瘤的临床特征和预后比较 |
topic | 论著 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364891/ https://www.ncbi.nlm.nih.gov/pubmed/32397019 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.07.006 |
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