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Published on: June 9, 2023
Burkitt's lymphoma presenting as a rapidly growing thyroid mass
Judith E Kalinyak1, Christina S Kong, I Ross McDougall
1Thyroid Clinic, Division of Nuclear Medicine, Stanford University School of Medicine, Stanford, California, USA.
Insights
This case report details a rare instance of Burkitt's lymphoma presenting as a rapidly growing thyroid mass. Prompt diagnosis and chemotherapy led to complete resolution of symptoms, highlighting the importance of rapid intervention for this aggressive lymphoma.
Area of Science:
- Oncology
- Hematology
- Pathology
Background:
- Burkitt's lymphoma is an aggressive non-Hodgkin lymphoma characterized by rapid proliferation.
- Primary thyroid lymphoma is rare, with most cases being non-Hodgkin lymphomas of B-cell origin.
Observation:
- A 53-year-old man presented with acute tracheal compression due to a rapidly enlarging thyroid mass.
- Fine-needle aspiration (FNA) biopsy suggested lymphoma, and CT scan confirmed tracheal deviation without invasion.
- The patient received emergent chemotherapy (CHOP and rituximab), resulting in rapid mass resolution.
Findings:
- Bone marrow biopsy confirmed stage IV Burkitt's lymphoma.
- The patient's treatment was escalated to hyper CVAD-R chemotherapy.
- Tumor lysis syndrome occurred but was successfully managed with hydration and allopurinol.
Implications:
- This case represents only the second reported instance of Burkitt's lymphoma presenting as a primary thyroid mass.
- The rapid progression and response to treatment underscore the need for urgent diagnosis and management.
- This rare presentation offers insights into primary thyroid lymphomas and their aggressive nature.
Abstract:
A 53-year-old man was admitted to the hospital because of tracheal compressive symptoms from a rapidly expanding thyroid mass. The patient first noticed the nodule less than a week prior to admission. Thyroid tests were normal. A fine-needle aspiration (FNA) biopsy showed a monotonous population of intermediate-sized lymphoid cells with scant cytoplasm suspicious for lymphoma. Twelve hours later an emergent computed tomography (CT) scan confirmed left tracheal deviation with compression, however, there were no signs of tumor invasion. The patient received emergent CHOP (clophosphamide, adriamycin, vincristine, prednisone) and rituxan therapy. His mass completely resolved within 36 hours. Bone marrow biopsy provided the final diagnosis of stage IV Burkitt's lymphoma and his therapy was changed to hyper CVAD-R chemotherapy (cytoxan, vincristine, adriamycin, dexamethasone, rituxan). The patient's hospital course was complicated by tumor lysis syndrome that was managed by hydration and allopurinol. To our knowledge, this is only the second reported case of Burkitt's lymphoma presenting as a thyroid mass. His presentation highlights the urgency in diagnosis and provides an opportunity to review a rare type of primary thyroid lymphoma.
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