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

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.

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Journal
Cureus
Published
2025-05-10
DOI
https://doi.org/10.7759/cureus.83842
Primary Topic
Lymphoma Diagnosis and Treatment
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article
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article

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

Cristina Monteiro, Luísa Pereira, Inês Vaz Arnaud, Nuno Gonçalves et al.
3 links
Cureus
Lymphoma Diagnosis and Treatment
article

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

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

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.

CureusVol. 17(5)
Administração Regional de Saúde de Lisboa e Vale do Tejo (PT)
Zero hunger
Openalex Percentile: Top 86%
Lymphoma Diagnosis and Treatment
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Primary Thyroid Mucosa-Associated Lymphoid Tissue (MALT) Lymphoma: A Case Report — Cristina Monteiro, Luísa Pereira, et al. · Cureus (2025) | TGRS Research Map | TGRS