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原发性甲状腺黏膜相关淋巴组织(MALT)淋巴瘤:一例报告

Primary Thyroid Mucosa-Associated Lymphoid Tissue (MALT) Lymphoma: A Case Report.

作者信息

Gonçalves Nuno, Monteiro Cristina, Calais Pereira Luísa, Lima Cláudia, Vaz Arnaud Inês

机构信息

General Surgery, Unidade Local de Saúde do Alto Minho, Viana do Castelo, PRT.

出版信息

Cureus. 2025 May 10;17(5):e83842. doi: 10.7759/cureus.83842. eCollection 2025 May.

Abstract

Primary thyroid lymphoma (PTL) is a rare entity. Mucosa-associated lymphoid tissue (MALT) lymphoma represents only a small portion of all PTLs and is usually associated with chronic lymphocytic thyroiditis. Most cases are indolent and asymptomatic, which may delay diagnosis. We present the case of a 63-year-old woman with a history of autoimmune hypothyroidism who developed a rapidly enlarging anterior neck mass and compressive symptoms. Ultrasound revealed an enlarged thyroid gland with a heterogeneous right lobe with a 34 mm lesion suggestive of focal thyroiditis. Fine-needle aspiration cytology was negative for malignancy (Bethesda II). Due to clinical progression, a total thyroidectomy was performed. Histopathological and immunohistochemical analyses confirmed MALT lymphoma. Primary MALT lymphoma of the thyroid is a rare and often underrecognized diagnosis. It should be considered in patients with chronic thyroiditis and new or enlarging nodules. Surgical excision may be both diagnostic and therapeutic in localized disease. Postoperative surveillance remains essential due to the potential for systemic involvement.

摘要

原发性甲状腺淋巴瘤(PTL)是一种罕见的疾病。黏膜相关淋巴组织(MALT)淋巴瘤仅占所有PTL的一小部分,通常与慢性淋巴细胞性甲状腺炎相关。大多数病例进展缓慢且无症状,这可能会延迟诊断。我们报告一例63岁女性病例,该患者有自身免疫性甲状腺功能减退病史,出现前颈部肿块迅速增大并伴有压迫症状。超声显示甲状腺肿大,右叶不均匀,有一个34 mm的病变,提示局灶性甲状腺炎。细针穿刺细胞学检查未发现恶性肿瘤(贝塞斯达II级)。由于临床症状进展,遂行甲状腺全切除术。组织病理学和免疫组织化学分析确诊为MALT淋巴瘤。甲状腺原发性MALT淋巴瘤是一种罕见且常未被充分认识的诊断。对于患有慢性甲状腺炎且出现新的或增大的结节的患者应考虑此病。手术切除对于局限性疾病可能兼具诊断和治疗作用。由于存在全身受累的可能性,术后监测仍然至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0bf/12147864/08d327e1aa8c/cureus-0017-00000083842-i01.jpg

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