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Abstract

Background

Primary thyroid lymphoma (PTL) is rare and diagnosis is challenging.

Methods

We conducted a multicenter retrospective study of patients with PTL from 1990 to 2023 to determine method of diagnosis, treatment, and outcomes.

Results

The study cohort included 31 patients with PTL; all had thyroid enlargement; 21 (68 ​%) had compressive symptoms, 11 (35 ​%) had hypothyroidism and 3 had (10 ​%) B symptoms. Diagnosis was established from incisional biopsy in 8 (26 ​%), needle biopsy in 4 (13 ​%), excisional lymph node biopsy in 1 (3 ​%), and thyroidectomy specimens in 18 (58 ​%). 15 (48 ​%) patients had Hashimoto thyroiditis. Treatment included chemotherapy in 19 (61 ​%); surgery alone in 7 (23 ​%); and radiation alone or with surgery in 5 (16 ​%) patients. One (3 ​%) patient recurred, and 4 (13 ​%) patients died after a median 4.2 years.

Conclusion

Diagnosis of PTL was made in only 13 ​% of patients preoperatively. There may be opportunity for needle biopsy to facilitate earlier diagnosis and treatment.

Details

Title
Primary thyroid lymphoma: A multi-center retrospective review
Author
Su, Marie W 1 ; Beck, Tim N 2 ; Knepprath, Jill 3 ; Romero-Velez, Gustavo 2   VIAFID ORCID Logo  ; Heiden, Katherine B 4 ; McHenry, Christopher R 1   VIAFID ORCID Logo 

 Case Western Reserve University School of Medicine, 9501 Euclid Ave, Cleveland, OH, 44106, USA; Department of Surgery, MetroHealth Medical Center, 2500 MetroHealth Dr, Cleveland, OH, 44109, USA 
 Department of Endocrine Surgery, Cleveland Clinic Foundation, 9500 Euclid Ave, Cleveland, OH, 44195, USA 
 Case Western Reserve University School of Medicine, 9501 Euclid Ave, Cleveland, OH, 44106, USA; Department of Surgery, University Hospitals Cleveland Medical Center, 11100 Euclid Ave, Cleveland, OH, 44106, USA 
 Case Western Reserve University School of Medicine, 9501 Euclid Ave, Cleveland, OH, 44106, USA; Department of Endocrine Surgery, Cleveland Clinic Foundation, 9500 Euclid Ave, Cleveland, OH, 44195, USA 
Section
Original Research Article
Publication year
2024
Publication date
Nov 2024
Publisher
Elsevier Limited
ISSN
00029610
e-ISSN
18791883
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3109787196
Copyright
©2024. Elsevier Inc.