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原发性甲状腺黏膜相关淋巴组织淋巴瘤:7例临床病理研究

Primary thyroid mucosa-associated lymphoid tissue lymphoma; a clinicopathological study of seven cases.

作者信息

Lee Seung Chul, Hong Soon Won, Lee Yong Sang, Jeong Jong Ju, Nam Kee-Hyun, Chung Woong Youn, Chang Hang-Seok, Park Cheong Soo

机构信息

Department of Surgery, Kangnam Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Korea.

出版信息

J Korean Surg Soc. 2011 Dec;81(6):374-9. doi: 10.4174/jkss.2011.81.6.374. Epub 2011 Nov 25.

DOI:10.4174/jkss.2011.81.6.374
PMID:22200037
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3243853/
Abstract

PURPOSE

Primary thyroid mucosa-associated lymphoid tissue (MALT) lymphoma is a very rare subgroup of thyroid lymphoma, accounting for about 6 to 28% of all primary thyroid lymphomas. The purpose of this study was to evaluate its clinicopathological features and treatment outcomes.

METHODS

We identified seven patients with thyroid MALT lymphoma who were treated between January 1997 and December 2007, and reviewed their clinicopathological features and follow-up outcomes.

RESULTS

There were five female and two male patients, and their mean age was 73 years. All patients presented with palpable neck mass. Two patients had hoarseness and dyspnea. All patients had a history of Hashimoto's thyroiditis with a mean of 175 months. Malignant lymphoma was suspected in only three patients using core needle biopsy. Four patients underwent thyroidectomy in the absence of preoperative pathologic confirmation, and histologic diagnosis was obtained after surgery. As initial treatment, complete surgical resection was performed in five patients, radiotherapy in one, and a combination of chemotherapy and radiotherapy in one. Six patients were alive for the mean follow-up period of 66 months and one patient died of unrelated causes. There were neither recurrences nor disease-specific mortalities.

CONCLUSION

When primary thyroid MALT lymphoma occurs in the thyroid or is confined to the neck, it responds well to local treatment such as surgical resection and external beam radiation therapy.

摘要

目的

原发性甲状腺黏膜相关淋巴组织(MALT)淋巴瘤是甲状腺淋巴瘤中非常罕见的一个亚组,约占所有原发性甲状腺淋巴瘤的6%至28%。本研究的目的是评估其临床病理特征和治疗结果。

方法

我们确定了1997年1月至2007年12月期间接受治疗的7例甲状腺MALT淋巴瘤患者,并回顾了他们的临床病理特征和随访结果。

结果

有5例女性和2例男性患者,平均年龄为73岁。所有患者均有可触及的颈部肿块。2例患者有声音嘶哑和呼吸困难。所有患者均有桥本甲状腺炎病史,平均病程为175个月。仅3例患者通过粗针活检怀疑为恶性淋巴瘤。4例患者在未获得术前病理确诊的情况下接受了甲状腺切除术,术后获得了组织学诊断。作为初始治疗,5例患者进行了完整的手术切除,1例接受了放疗,1例接受了化疗和放疗联合治疗。6例患者在平均66个月的随访期内存活,1例患者死于无关原因。既无复发也无疾病特异性死亡。

结论

当原发性甲状腺MALT淋巴瘤发生于甲状腺或局限于颈部时,对手术切除和外照射放疗等局部治疗反应良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eb7/3243853/aec75dbca107/jkss-81-374-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eb7/3243853/aec75dbca107/jkss-81-374-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eb7/3243853/aec75dbca107/jkss-81-374-g001.jpg

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