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The Primary Thyroid Lymphoma Treated by Surgery without Chemotherapy: Two Cases Reports / 대한내분비외과학회지
Korean Journal of Endocrine Surgery ; : 51-55, 2016.
Artigo em Inglês | WPRIM | ID: wpr-219304
ABSTRACT
Primary thyroid lymphoma (PTL) is a relatively rare disease, accounting for less than 0.5~5% of all thyroid malignancies. We encountered two cases of a primary thyroid lymphoma with Hashimoto's thyroiditis; one in a 63-year-old man and the other in a 79-year-old woman. The first case was a mucosa-associated lymphoid tissue lymphoma, and the other was a diffuse large B-cell lymphoma. Both patients underwent surgery and radiotherapy after being diagnosed using fine-needle aspiration cytology (FNAC). Both patients recovered well with no recurrence throughout the study period. The role of the surgeon in the treatment and diagnosis of thyroid lymphoma has been reduced due to the development of FNAC and combination therapy with chemotherapy and radiotherapy. On the other hand, surgery can be an effective treatment option for PTL confined to the thyroid, for achieving a definitive diagnosis, and in the treatment of patients with an airway obstruction.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Radioterapia / Recidiva / Glândula Tireoide / Tireoidectomia / Tireoidite / Linfoma de Células B / Linfoma de Zona Marginal Tipo Células B / Doenças Raras / Biópsia por Agulha Fina / Diagnóstico Tipo de estudo: Estudo diagnóstico Limite: Idoso / Feminino / Humanos Idioma: Inglês Revista: Korean Journal of Endocrine Surgery Ano de publicação: 2016 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Radioterapia / Recidiva / Glândula Tireoide / Tireoidectomia / Tireoidite / Linfoma de Células B / Linfoma de Zona Marginal Tipo Células B / Doenças Raras / Biópsia por Agulha Fina / Diagnóstico Tipo de estudo: Estudo diagnóstico Limite: Idoso / Feminino / Humanos Idioma: Inglês Revista: Korean Journal of Endocrine Surgery Ano de publicação: 2016 Tipo de documento: Artigo