Romanian Journal of Medical Practice (Dec 2021)

Primary thyroid lymphoma

  • Mara Carsote,
  • Diana Elena Rentea,
  • Claudia Mehedintu,
  • Stefania Zugravu,
  • Anda Dumitrascu,
  • Florica Sandru,
  • Mihai Cristian Dumitrascu

DOI
https://doi.org/10.37897/RJMP.2021.4.12
Journal volume & issue
Vol. 16, no. 4
pp. 466 – 468

Abstract

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Primary thyroid lymphoma represents a challenging, multi-disciplinary condition that it may be found in addition to positive antibodies against thyroid. Early recognition is essential for an adequate management. A thyroid nodule but usually the entire goiter may rapidly progress to a voluminous mass causing local compressive symptoms. Most of the patients with primary thyroid lymphoma had a history of Hashimoto thyroiditis. Epidemiologically, primary thyroid lymphoma represents an exceptional entities opposite to papillary or follicular cancer. The first tool of evaluation is ultrasound; in order to appreciate the local and distance invasion, computed tomography is useful. Fine needle aspiration and cell block analysis or biopsy and immunohistochemistry report are essential for adequate diagnostic in order to avoid unnecessary surgery. Diffuse large B-cell lymphoma is the most frequent histological type. Chemotherapy and local radiation represents the elective management. Considering this unusual condition, awareness is the key operative word for different practitioners.

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