[Thymic Neuroendocrine Tumor Associated with Multiple Endocrine Neoplasia Type 1].
Kyobu Geka
; 76(4): 324-327, 2023 Apr.
Article
en Ja
| MEDLINE
| ID: mdl-36997182
ABSTRACT
Multiple endocrine neoplasia (MEN) type 1 is a hereditary syndrome characterized by hyperplasia and adenoma of the parathyroid gland, pancreatic tumor, and pituitary tumor. We report a rare case of thymic neuroendocrine tumor diagnosed after removal of a thymic tumor following pancreatic and parathyroid surgery. A 35-year-old man was diagnosed with MEN type 1 by hypercalcemia and gastrinemia with a ureteral tone. Two well defined nodules in the anterior mediastinum on computed tomography (CT), and a high degree of accumulation on positron emission tomography (PET) was noted. Surgery was performed through a median sternotomy with anterior mediastinal tumor resection. Pathology showed thymic neuroendocrine tumor (NET). Immunostaining results were different from pancreatic NET and duodenal NET, and a diagnosis of primary thymic NET was made. Postoperative radiation therapy was completed as adjuvant therapy, and the patient is alive without reccurrence.
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Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Timoma
/
Neoplasias del Timo
/
Tumores Neuroendocrinos
/
Neoplasia Endocrina Múltiple Tipo 1
Tipo de estudio:
Risk_factors_studies
Límite:
Adult
/
Humans
/
Male
Idioma:
Ja
Revista:
Kyobu Geka
Año:
2023
Tipo del documento:
Article
País de afiliación:
Japón