A Case of Parathyroid Carcinoma Invading Thyroid Gland as Solitary Nodular Form / 대한내분비학회지
Journal of Korean Society of Endocrinology
;
: 171-176, 1999.
Artículo
en Coreano
| WPRIM
| ID: wpr-119795
ABSTRACT
Parathyroid carcinoma is a rare cause of primary hyperparathyroidism and commonly metastasize to lymph node, lung, liver, and bone. In Korea, there has been no report of distant metastasis in parathyroid carcinoma except for one case of pulmonary metastasis. A 58-year-old man presenting with weakness, nausea, and a palpable thyroid nodule visited our hospital. Elevated serum calcium and parathyroid hormone (PTH) concentration allowed the diagnosis of hyperparathyroidism. Two discrete masses were identified by neck ultrasound scan, computed tomography (CI') and Tc-Sestamibi scan in the left lobe of thyroid gland and ipsilateral parathyroid gland. So multiple endocrine neoplasia (MEN) type 2A" was suspected initially, but postoperative histological diagnosis was left parathyroid carcinoma with solitary nodular lesion invading left thyroid gland. He was successfully treated with left parathyroidectomy and left thyroid lobectomy.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Hormona Paratiroidea
/
Neoplasias de las Paratiroides
/
Glándulas Paratiroides
/
Glándula Tiroides
/
Neoplasia Endocrina Múltiple
/
Calcio
/
Paratiroidectomía
/
Ultrasonografía
/
Nódulo Tiroideo
/
Neoplasia Endocrina Múltiple Tipo 2a
Tipo de estudio:
Estudio diagnóstico
/
Estudio pronóstico
Límite:
Humanos
País/Región como asunto:
Asia
Idioma:
Coreano
Revista:
Journal of Korean Society of Endocrinology
Año:
1999
Tipo del documento:
Artículo
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