Ann Surg Treat Res.  2015 Dec;89(6):295-299. 10.4174/astr.2015.89.6.295.

Clinicopathological characteristics and treatment outcomes of 38 cases of primary thyroid lymphoma: a multicenter study

Affiliations
  • 1Department of Surgery, Seoul National University Boramae Medical Center, Seoul, Korea.
  • 2Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea. kyueunlee@snu.ac.kr
  • 3Department of Surgery, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • 4Department of Surgery, Inje University Haeundae Paik Hospital, Inje University College of Medicine, Busan, Korea.
  • 5Department of Surgery, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.

Abstract

PURPOSE
Primary thyroid lymphoma (PTL) is a rare disease and it has been investigated in a limited number of studies. The present multicenter study evaluated the clinical features and treatment outcomes of PTL.
METHODS
The medical records of patients diagnosed with PTL between 2000 and 2013 in three centers were retrospectively reviewed.
RESULTS
The study included 11 men and 27 women with a median age of 63.3 years (range, 42-83 years). The median follow-up was 56.0 months (range, 3-156 months). Of the 38 patients included, 16 had mucosa-associated lymphoid tissue (MALT) lymphoma, six had mixed MALT and diffuse large B-cell lymphoma (DLBCL), and 16 had DLBCL. Thirty-five patients (92.1%) had early stage (stage I/II) disease. Of the 16 MALT lymphoma patients, 14 were treated by surgery, and radiotherapy (RT) or chemotherapy was combined in five patients. Two patients received RT or chemotherapy alone. Of the six mixed MALT and DLBCL patients, three underwent surgery with chemotherapy and three underwent chemotherapy alone, RT alone, or surgery with RT. All of the 16 DLBCL patients received chemotherapy, and surgery and RT was combined in 4 and 1 patients, respectively. The 5-year survival was 100% for MALT lymphoma (7 of 7) and mixed MALT and DLBCL patients (5 of 5) and 87.5% for DLBCL patients (7 of 8).
CONCLUSION
Early stage PTL has an excellent prognosis when managed by single or combined treatment modalities. Clinicians should consider PTL in patients with underlying Hashimoto's thyroiditis presenting with an enlarging thyroid mass.

Keyword

Lymphoma; Thyroid lymphoma; Primary thyroid lymphoma; Marginal zone B-cell lymphoma; Diffuse Large B-cell lymphoma

MeSH Terms

Drug Therapy
Female
Follow-Up Studies
Humans
Lymphoid Tissue
Lymphoma*
Lymphoma, B-Cell
Lymphoma, B-Cell, Marginal Zone
Male
Medical Records
Prognosis
Radiotherapy
Rare Diseases
Retrospective Studies
Thyroid Gland*
Thyroiditis

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Primary Thyroid Lymphoma with Vocal Fold Paralysis
Jae Yeong Jeong, Chang Myeon Song, Yong Bae Ji, Kyung Tae
Int J Thyroidol. 2023;16(2):209-213.    doi: 10.11106/ijt.2023.16.2.209.


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