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Primary Thyroid Lymphoma: A Case Series
Yousef Alalawi1, Tahani N Alrashidi1, Sarah Shafie1
1Department of Surgery, King Salman Armed Forces Hospital, Tabuk, SAU.
Cureus
|September 3, 2025
Summary
Primary thyroid lymphoma (PTL), often linked to Hashimoto's thyroiditis, typically presents as a fast-growing thyroid mass. Core needle biopsy is crucial for diagnosing diffuse large B-cell lymphoma (DLBCL), the predominant PTL subtype.
Area of Science:
- Oncology
- Pathology
- Endocrinology
Background:
- Primary thyroid lymphoma (PTL) is a rare malignancy.
- PTL frequently co-occurs with Hashimoto's thyroiditis.
- Treatment for PTL differs from other thyroid cancers.
Purpose of the Study:
- To investigate the clinical presentation of PTL.
- To evaluate diagnostic methods for PTL.
- To analyze treatment strategies for PTL.
Main Methods:
- Retrospective case series of seven PTL patients (2017-2021).
- Data collected on clinical presentation, diagnosis, and treatment.
- Histopathological examination confirmed diffuse large B-cell lymphoma (DLBCL).
Main Results:
- Seven patients (5 female, 2 male; mean age 57.8) diagnosed with PTL.
- Four patients had co-existing Hashimoto's thyroiditis.
- Rapidly enlarging thyroid mass with compression symptoms was common.
- Core needle biopsy and surgical excision were diagnostic.
- All cases confirmed as DLBCL.
- Mortality observed in two patients (stages III and IV).
Conclusions:
- Rapidly growing thyroid mass with Hashimoto's thyroiditis suggests PTL.
- DLBCL is the predominant PTL subtype.
- Core needle biopsy is superior to fine-needle aspiration cytology (FNAC) for diagnosis.
- Surgery is primarily diagnostic; prognosis depends on disease stage.
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