Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Eui Dal Jung"'
Publikováno v:
Kosin Medical Journal, Vol 33, Iss 3, Pp 446-453 (2018)
Pheochromocytomas might be sporadic or genetic. Genetic pheochromocytoma is associated with multiple endocrine neoplasia (MEN) type 2A, MEN type 2B, and von Hippel-Lindau (VHL) disease. RET mutations are identified in more than 90% of index cases of
Externí odkaz:
https://doaj.org/article/45bf55bcc8bf4f2d81e3444008725887
Publikováno v:
Endocrinology and Metabolism, Vol 30, Iss 2, Pp 221-225 (2015)
Neuroendocrine lesions of the thyroid are rare. The most common types are medullary thyroid carcinomas (MTCs) and C-cell hyperplasia. MTCs originate from thyroid parafollicular cells that secrete calcitonin which serves as a serum marker of MTCs. Her
Externí odkaz:
https://doaj.org/article/e62b8d0f90ef469088b55fb4f7aa4799
Autor:
Eon Ju Jeon, Eui Dal Jung
Publikováno v:
Endocrinology and Metabolism, Vol 29, Iss 1, Pp 33-39 (2014)
BackgroundA diagnostic whole-body scan (WBS) is recommended 6 to 12 months after total thyroidectomy and radioactive iodide ablation in intermediate- or high-risk patients with differentiated thyroid cancer (DTC). The aim of this study was to evaluat
Externí odkaz:
https://doaj.org/article/cb2d34162e264db7b02724df4bad7855
Publikováno v:
Kosin Medical Journal, Vol 28, Iss 2, Pp 183-186 (2013)
Addison’s disease is a rare disorder that causes fatigue, genral weakness, weight loss, pigmentation due to adrenal hypofunction and it’s underlying causes are various. We report a case of 42-year-old man with fatigue, generalized cutaneous pigme
Externí odkaz:
https://doaj.org/article/fd4b7d6422154ed0bd6603fa5d0ff037
Publikováno v:
Case Reports in Endocrinology, Vol 2016 (2016)
Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT) of the thyroid gland is uncommon. Even though its natural history is not well defined, it is known to be indolent course. We present a case of primary MALT thyroid lymphoma
Externí odkaz:
https://doaj.org/article/eee9e487017d42e18b109312a4a5c115
Autor:
Eon Ju Jeon, Eui Dal Jung
Publikováno v:
Endocrinology and Metabolism, Vol 29, Iss 2, Pp 208-209 (2014)
Externí odkaz:
https://doaj.org/article/0ef96e00d2054f28ad278128fdd67187
Publikováno v:
Kosin Medical Journal. 33:446-453
Pheochromocytomas might be sporadic or genetic. Genetic pheochromocytoma is associated with multiple endocrine neoplasia (MEN) type 2A, MEN type 2B, and von Hippel-Lindau (VHL) disease. RET mutations are identified in more than 90% of index cases of
Publikováno v:
Case Reports in Endocrinology, Vol 2016 (2016)
Case Reports in Endocrinology
Case Reports in Endocrinology
Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT) of the thyroid gland is uncommon. Even though its natural history is not well defined, it is known to be indolent course. We present a case of primary MALT thyroid lymphoma
Publikováno v:
The Korean Journal of Medicine. 89:340-345
Adrenal myelolipoma (AML) is a rare, usually benign, and nonfunctioning tumor. About 7-15% of adrenal incidentalomas are AMLs, composed of normal hematopoietic elements and mature adipose tissue. AML is usually unilateral and < 4 cm. It is often disc
Publikováno v:
Endocrinology and Metabolism, Vol 30, Iss 2, Pp 221-225 (2015)
Endocrinology and Metabolism
Endocrinology and Metabolism
Neuroendocrine lesions of the thyroid are rare. The most common types are medullary thyroid carcinomas (MTCs) and C-cell hyperplasia. MTCs originate from thyroid parafollicular cells that secrete calcitonin which serves as a serum marker of MTCs. Her