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与桥本甲状腺炎相关的原发性甲状腺伯基特淋巴瘤伪装成新冠后甲状腺炎

Primary Burkitt Lymphoma of the Thyroid Associated With Hashimoto Thyroiditis Masquerading as Post-COVID Thyroiditis.

作者信息

Thewjitcharoen Yotsapon, Chatchomchuan Waralee, Wanothayaroj Ekgaluck, Veerasomboonsin Veekij, Keelawat Somboon, Himathongkam Thep

机构信息

THEPTARIN Diabetes, Thyroid and Endocrine Center, Vimut-Theptarin Hospital, Bangkok 10110, Thailand.

Department of Radiology, Vimut-Theptarin Hospital, Bangkok 10110, Thailand.

出版信息

JCEM Case Rep. 2025 Aug 14;3(9):luaf178. doi: 10.1210/jcemcr/luaf178. eCollection 2025 Sep.

Abstract

Primary thyroid lymphoma accounts for only 2% to 5% of all thyroid tumors, and Burkitt lymphoma of the thyroid is even rarer than other types of B-cell lymphoma. It is a highly aggressive non-Hodgkin lymphoma characterized by intermediate-sized lymphoid cells with a "starry sky" appearance and exhibits chromosomal translocations that activate the oncogene. A male predominance and an aggressive clinical course with a high risk of central nervous system involvement and tumor lysis syndrome are all well-recognized features of Burkitt lymphoma. We present a case of a 28-year-old man with primary Burkitt lymphoma of the thyroid initially misdiagnosed as post-COVID thyroiditis. Core needle biopsy showed round, intermediate-sized lymphoid cells admixed with scattered tingible body macrophages displaying a "starry sky" appearance. Following the final histological diagnosis of primary thyroid Burkitt lymphoma, the patient received intensive chemotherapy. Six months after the diagnosis, the patient succumbed to disease progression, causing upper airway obstruction. Primary Burkitt lymphoma of the thyroid can cause pain and other symptoms due to the rapidly growing mass in the neck. Adequate pathological diagnosis with core needle biopsy rather than fine needle aspiration is essential for treatment planning and outcome improvement.

摘要

原发性甲状腺淋巴瘤仅占所有甲状腺肿瘤的2%至5%,甲状腺伯基特淋巴瘤比其他类型的B细胞淋巴瘤更为罕见。它是一种侵袭性很强的非霍奇金淋巴瘤,其特征是中等大小的淋巴细胞呈现“星空”样外观,并表现出激活癌基因的染色体易位。男性居多以及具有中枢神经系统受累和肿瘤溶解综合征高风险的侵袭性临床病程都是伯基特淋巴瘤公认的特征。我们报告一例28岁男性原发性甲状腺伯基特淋巴瘤病例,最初被误诊为新冠后甲状腺炎。粗针活检显示圆形、中等大小的淋巴细胞与散在的含铁血黄素巨噬细胞混合,呈现“星空”样外观。在原发性甲状腺伯基特淋巴瘤最终组织学诊断后,患者接受了强化化疗。诊断后六个月,患者因疾病进展死亡,导致上呼吸道梗阻。甲状腺原发性伯基特淋巴瘤可因颈部迅速增大的肿块而引起疼痛和其他症状。对于治疗规划和改善预后,通过粗针活检而非细针穿刺进行充分的病理诊断至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2257/12352296/9de4c8349d15/luaf178f1.jpg

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