原发性甲状腺淋巴瘤:用Polatuzumab Vedotin治疗的罕见诊断。

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
Rupam Sharma, Arin Orogian, Ralph Garcia-Pacheco, Tung Trang, Matthew Clarke, William Stull, Stanley Kim
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引用次数: 0

摘要

原发性甲状腺淋巴瘤是起源于甲状腺的一种罕见而独特的结外淋巴瘤。它在所有甲状腺恶性肿瘤中占不到5%,在结外淋巴瘤中占2%。它主要影响老年人,女性发病率较高。患者通常表现为甲状腺肿块迅速增大,伴有吞咽困难、呼吸困难和声音嘶哑等压迫性临床症状。诊断需要结合细针穿刺、核心针活检和先进的成像技术。标准治疗包括化疗的多模式策略,通常还需辅以放疗和手术干预。本文介绍的是首例用Pola-R-CHP治疗弥漫大B细胞淋巴瘤的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Thyroid Lymphoma: A Rare Diagnosis Treated With Polatuzumab Vedotin.

Primary thyroid lymphoma is one of the rare and distinct type of extra nodal lymphomas originating within the thyroid gland. It accounts for less than 5% of all thyroid malignancies and 2% of extra nodal lymphomas. It predominantly affects older adults, with a higher incidence in women. Patients typically present with a rapidly enlarging thyroid mass, accompanied by clinical symptoms of compression such as dysphagia, dyspnea, and hoarseness. Diagnosis is established through a combination of fine-needle aspiration, core needle biopsy, and advanced imaging techniques. Standard treatment involves a multimodal strategy of chemotherapy, often with the addition of radiotherapy and surgical intervention. Herein presented is the first reported case of diffuse large B-cell lymphoma treated with Pola-R-CHP.

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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
165
审稿时长
12 weeks
期刊介绍: The AFMR is committed to enhancing the training and career development of our members and to furthering its mission to facilitate the conduct of research to improve medical care. Case reports represent an important avenue for trainees (interns, residents, and fellows) and early-stage faculty to demonstrate productive, scholarly activity.
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