Primary thyroid lymphoma: A multi-center retrospective review

IF 2.7 3区 医学 Q1 SURGERY American journal of surgery Pub Date : 2024-11-01 Epub Date: 2024-08-22 DOI:10.1016/j.amjsurg.2024.115927
Marie W. Su , Tim N. Beck , Jill Knepprath , Gustavo Romero-Velez , Katherine B. Heiden , Christopher R. McHenry
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Abstract

Background

Primary thyroid lymphoma (PTL) is rare and diagnosis is challenging.

Methods

We conducted a multicenter retrospective study of patients with PTL from 1990 to 2023 to determine method of diagnosis, treatment, and outcomes.

Results

The study cohort included 31 patients with PTL; all had thyroid enlargement; 21 (68 ​%) had compressive symptoms, 11 (35 ​%) had hypothyroidism and 3 had (10 ​%) B symptoms. Diagnosis was established from incisional biopsy in 8 (26 ​%), needle biopsy in 4 (13 ​%), excisional lymph node biopsy in 1 (3 ​%), and thyroidectomy specimens in 18 (58 ​%). 15 (48 ​%) patients had Hashimoto thyroiditis. Treatment included chemotherapy in 19 (61 ​%); surgery alone in 7 (23 ​%); and radiation alone or with surgery in 5 (16 ​%) patients. One (3 ​%) patient recurred, and 4 (13 ​%) patients died after a median 4.2 years.

Conclusion

Diagnosis of PTL was made in only 13 ​% of patients preoperatively. There may be opportunity for needle biopsy to facilitate earlier diagnosis and treatment.

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原发性甲状腺淋巴瘤多中心回顾性研究
背景原发性甲状腺淋巴瘤(PTL)非常罕见,诊断具有挑战性。方法我们对1990年至2023年的PTL患者进行了一项多中心回顾性研究,以确定诊断方法、治疗和预后。结果研究队列包括31例PTL患者;所有患者均有甲状腺肿大;21例(68%)有压迫症状,11例(35%)有甲状腺功能减退,3例(10%)有B症状。8例(26%)通过切口活检确诊,4例(13%)通过针刺活检确诊,1例(3%)通过切除淋巴结活检确诊,18例(58%)通过甲状腺切除术标本确诊。15例(48%)患者患有桥本甲状腺炎。治疗方法包括:19 例(61%)患者接受化疗;7 例(23%)患者接受单纯手术治疗;5 例(16%)患者接受单纯放疗或手术治疗。1例(3%)患者复发,4例(13%)患者在中位4.2年后死亡。针刺活检可能有助于早期诊断和治疗。
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来源期刊
CiteScore
5.00
自引率
6.70%
发文量
570
审稿时长
56 days
期刊介绍: The American Journal of Surgery® is a peer-reviewed journal designed for the general surgeon who performs abdominal, cancer, vascular, head and neck, breast, colorectal, and other forms of surgery. AJS is the official journal of 7 major surgical societies* and publishes their official papers as well as independently submitted clinical studies, editorials, reviews, brief reports, correspondence and book reviews.
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