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Updated: Jun 19, 2026

Transoral Robotic Total Thyroidectomy and Bilateral Central Regional Lymph Node Dissection for Papillary Thyroid Carcinoma
Published on: September 15, 2023
[Primary thyroid lymphoma. Report of four cases]
Patricio Gac E1, Patricio Cabané T, José Amat V
1Departamento de Cirugía, Equipo Cirugía Endocrina, Cabeza y Cuello, Hospital Clínico de la Universidad de Chile, Santiago de Chile. patriciogac@yahoo.com.ar
Primary thyroid lymphoma, a rare non-Hodgkin type cancer, presents varied outcomes. Treatment success, like in a 16-year-old patient, contrasts with cases lost to follow-up or succumbing to complications.
Area of Science:
- Oncology
- Hematology
- Endocrinology
Background:
- Primary thyroid lymphoma is a rare malignancy, typically of the non-Hodgkin lymphoma subtype.
- Understanding its clinical presentation and treatment response is crucial for patient management.
Observation:
- This report details four female patients diagnosed with primary thyroid lymphoma.
- Patient ages ranged from 16 to 81 years.
- Clinical courses varied significantly among the cases.
Findings:
- One 16-year-old patient achieved disease-free status after surgery and chemotherapy.
- An 81-year-old patient received surgery and chemotherapy but was lost to follow-up.
- An 80-year-old patient died post-operatively from multiple organ failure.
- A 54-year-old patient, post-surgery, rejected chemotherapy and was lost to follow-up.
Implications:
- The diverse outcomes highlight the heterogeneous nature of primary thyroid lymphoma.
- Treatment adherence, including chemotherapy, appears critical for favorable prognoses.
- Further research into optimal management strategies for this rare condition is warranted.
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