- Scintigraphic evaluation of multiple endocrine neoplasia type 2 (MEN type 2)
-
Lee JT, Lee KB, Whang KS, Kim BW, Lee IK
- KMID: 1686044
- Korean J Nucl Med.
- 1991 May;25(1):122-128.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Multiple Endocrine Neoplasia and Familial Medullary Thyroid Carcinoma
-
Choi YS
- KMID: 2095101
- J Korean Thyroid Assoc.
- 2012 Nov;5(2):124-131.
- doi: 10.11106/jkta.2012.5.2.124
Multiple endocrine neoplasia (MEN) is defined as a disorder with neoplasms in two or more different hormonal tissues in several members of a family. MEN1, or Wermer's syndrome, is inherited... -
- CITED
-
- Close
- SHARE
-
- Close
- Ectopic ACTH Syndrome with Bilateral Pheochromocytoma in Multiple Endocrine Neoplasia Type 2A
-
Moon JM, Kim YJ, Seo YJ, Choi HY, Kim JH, Park JR, Lee YJ, Kim HY, Kim SG, Choi DS
- KMID: 1468546
- J Korean Endocr Soc.
- 2009 Dec;24(4):265-271.
- doi: 10.3803/jkes.2009.24.4.265
Multiple endocrine neoplasia type 2A (MEN 2A) is an autosomal dominant syndrome characterized by the presence of medullary thyroid carcinoma, pheochromocytoma, and hyperparathyroidism. MEN 2A arises due to a germline... -
- CITED
-
- Close
- SHARE
-
- Close
- A family of multiple endocrine neoplasia type 2A associated with a C618R mutation in RET proto-oncogene
-
Kim NH, Kim JH, Nam JH, Park JP, Park JE, Choi YS, Park YH
- KMID: 1833332
- Korean J Med.
- 2006 Apr;70(4):448-454.
Medullary thyroid carcinoma (MTC) is a relatively rare malignant thyroid disease that accounts for approximately 1% to 5% of all thyroid carcinomas. MTC occurs as a sporadic disease and as... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Multiple endocrine neoplasia type 2a
-
Hong SJ, Yang IM, Woo JT, Kim JW, Kim YS, Choi YK, Yun YS, Lee CH, Lee SH, Kim DY, Kim SW
- KMID: 2331074
- J Korean Soc Endocrinol.
- 1997 Jun;12(2):328-337.
Multiple endocrine neoplasia type2a (MEN type2a) is a dominantly inherited cancer syndrome which is characterized by medullary thyroid carcinoma, pheochromocytoma and parathyroid hyperplasia or adenoma. Recent reports show that DNA... -
- CITED
-
- Close
- SHARE
-
- Close
- Recurrent hyperparathyroidism due to proliferation of autotransplanted parathyroid tissue in a multiple endocrine neoplasia type 2A patient
-
Kim BK, Lee J, Sun WY
- KMID: 2350542
- Ann Surg Treat Res.
- 2016 Sep;91(3):145-148.
- doi: 10.4174/astr.2016.91.3.145
About 20%–30% of all cases of multiple endocrine neoplasia type 2A (MEN 2A) is accompanied by primary hyperparathyroidism. These patients undergo parathyroidectomy and, if needed, autotransplantation. In rare cases, autotransplanted... -
- CITED
-
- Close
- SHARE
-
- Close
- Cermline Mutation of RET Gene in A Multiple Endocrine Neoplasia Type 2A ( MEN2A ) Family
-
Yang HY, Park YJ, Kwon HJ, Choe KJ
- KMID: 2059283
- J Korean Cancer Assoc.
- 1999 Oct;31(5):867-875.
PURPOSE: Multiple Endocrine Neoplasia Type 2A (MEN 2A) is an autosomal dominant disease characterized by development of the medullary thyroid cancer, adrenal pheochromocytoma and parathyroid hyperplasia. Gennline mutations of RET... -
- CITED
-
- Close
- SHARE
-
- Close
- Anesthetic Management for Bilateral Pheochromocytomas in Multiple Endocrine Neoplasia Type 2a
-
Lee HS
- KMID: 2090726
- Korean J Anesthesiol.
- 1992 Jun;25(3):631-635.
- doi: 10.4097/kjae.1992.25.3.631
Multiple endocrine neoplasis type 2a(MEN 2a) is an inherited syndrome characterized by the occurrence of medullary thyroid carcinoma, parathyroid hyperplasia and adrenal pheochromocytoma. Adrenal Medullary disease varies from hyperplasia to... -
- CITED
-
- Close
- SHARE
-
- Close
- A Family Presenting with Catastrophic Features due to Pheochromocytoma Associated with Multiple Endocrine Neoplasia 2A
-
Lee YJ, Chon S, Lee SH, Lee TW, Ihm CG, Noh TJ, Oh S, Woo JT, Kim SW, Kim JW, Kim YS
- KMID: 2169020
- Endocrinol Metab.
- 2010 Jun;25(2):135-141.
- doi: 10.3803/EnM.2010.25.2.135
Multiple endocrine neoplasia 2A (MEN 2A) is an autosomal dominant disease that consists of medullary thyroid carcinoma (MTC), pheochromocytoma and parathyroid hyperplasia. The activation of germ-line mutations in the RET... -
- CITED
-
- Close
- SHARE
-
- Close
- A Family of Multiple Endocrine Neoplasia Type 2A with a C634R Mutation and a G691S Polymorphism in RET Proto-oncogene
-
Yun SW, Yoo WS, Hong KH, Kim BH, Kang MH, Choo YK, Park HY, Kim DH, Chung HK, Chang MC, Kwon MS, Kim HJ
- KMID: 1958911
- J Korean Endocr Soc.
- 2007 Dec;22(6):453-459.
- doi: 10.3803/jkes.2007.22.6.453
Multiple endocrine neoplasia type 2A (MEN2A) is an autosomal dominant syndrome characterized by the presence of a medullary thyroid carcinoma, pheochromocytoma and hyperparathyroidism. MEN2A arises due to germline missense mutations... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Calcitonin Secreting Pheochromocytoma
-
Byun JW, Shin YG, Chung CH, Won YJ, Choi YJ, Park ER, Lee MD, Song CH, Cho MY, Kang SJ
- KMID: 2461642
- J Korean Soc Endocrinol.
- 1996 Sep;11(3):343-347.
Pheochromocytoma is a catecholamine producing turnor and raise with less than 0.1% of hypertensive patients. It is developed, most commonly, in sporadic pheochromocytoma or multiple endocrine neoplasia type 2. Therefore,... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Multiple Endocrine Neoplasia 2A with Germ Line Mutation of RET Gene
-
Kim HY, Lee JY, Kim SB, Lee KW, Seo JA, Oh JH, Kim SG, Choi KM, Baik SH, Choi DS, Kim NH
- KMID: 2331186
- J Korean Soc Endocrinol.
- 2003 Oct;18(5):481-488.
Multiple endocrine neoplasia 2A (MEN 2A) is an autosomal dominantly inherited disease, composed of medullary thyroid carcinoma, pheochromocytoma and hyperparathyroidism. The activation of germ-line mutations in the RET proto-oncogene are... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Papillary Thyroid Carcinoma Combined with Multiple Endocrine Neoplasia Type 2A
-
Kim JK, Chung HW, Seo HS, Kim DJ, Chung SS, Song YD, Kwon KH, Jin YM, Lee MK, Lim SK, Kim IJ, Kang HC, Park JH, Park JG
- KMID: 2200061
- J Korean Soc Endocrinol.
- 2002 Oct;17(5):730-738.
Multiple endocrine neoplasia (MEN) type 2A is a syndrome of medullary thyroid carcinomas, pheochromocytomas and parathyroid hyperplasia. The simultaneous occurrence of medullary, and papillary, thyroid carcinomas is rare because they... -
- CITED
-
- Close
- SHARE
-
- Close
- A case of breast cancer in a patient with multiple endocrine neoplasia type 2
-
Roh JM, Lee YB, An HR, Shim WH, Lee EH, Hong SW, Cho MH
- KMID: 2259348
- Korean J Med.
- 2010 Oct;79(4):432-437.
Multiple Endocrine Neoplasia Type 2 (MEN2) is a rare hereditary complex disorder characterized by the presence of medullary thyroid carcinoma, pheochromocytoma, and other hyperplasias or neoplasias of different endocrine tissues... -
- CITED
-
- Close
- SHARE
-
- Close
- Two Cases of Multiple Endocrine Neoplasia Type II with RET Mutaion
-
Yoo SY, Choi YH, Lee MK, Kim MS, Hwang PH
- KMID: 2279829
- Clin Pediatr Hematol Oncol.
- 2014 Oct;21(2):163-167.
- doi: 10.0000/cpho.2014.21.2.163
Multiple endocrine neoplasia type 2(MEN2) is a rare autosomal dominant inherited disorder characterized by the presence of medullary thyroid carcinoma, pheochromocytoma and other hyperplasia and/or neoplasia of different endocrine tissues... -
- CITED
-
- Close
- SHARE
-
- Close
- Analysis of RET Gene Point Mutation in a Family with Multiple Endocrine Neoplasia Type 2A
-
Kim SW, Lee KD, Kim JY, Moon HS, Kim YR, Park YH, Lee KS
- KMID: 2276772
- Korean J Otolaryngol-Head Neck Surg.
- 2007 Jun;50(6):529-536.
BACKGROUND AND OBJECTIVES: Multiple Endocrine Neoplasia type 2A (MEN 2A) is a syndrome that encompasses medullary thyroid carcinoma, pheochromocytoma, and hyperparathyroidism. Since MEN 2A is inherited as autosomal dominant, early... -
- CITED
-
- Close
- SHARE
-
- Close
- The Characteristics of Multiple Endocrine Neoplasia in Korean
-
Yang JH, Woo SU
- KMID: 2375964
- Korean J Endocr Surg.
- 2005 Jun;5(1):1-6.
- doi: 10.16956/kjes.2005.5.1.1
PURPOSE: Multiple Endocrine Neoplasm (MEN) is a rare, complex and familial disease. There are MEN syndromes are inherited in an autosomal dominant fashion with high penetrance. The variations in the... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Parathyroid Carcinoma Invading Thyroid Gland as Solitary Nodular Form
-
Choi YK, Lee JS, Kim HW, Kim YM, Son SM, Kim IJ, Kim YK, Chae HJ
- KMID: 2331148
- J Korean Soc Endocrinol.
- 1999 Mar;14(1):171-176.
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... -
- CITED
-
- Close
- SHARE
-
- Close
- Small Medullary Thyroid Cancer Dectected by Genetic Mutation Screening in Men IIa Family
-
Chung JH, Kim KW, Kim JE, Kim BJ, Kim SH, Kim KA, Lee MS, Lee MG
- KMID: 2142210
- J Korean Soc Endocrinol.
- 1998 Jun;13(2):230-239.
Multiple endocrine neoplasia (MEN) Ila is an inherited disease characterized by the development of medullary thyroid carcinoma, pheochromocytoma and hyperparathyroidism. It has been shown to be associated with germ-line mutatians... -
- CITED
-
- Close
- SHARE
-
- Close
- Pheochromocytoma Developed in a Boy with Multiple Endocrine Neoplasia Type 2A Confirmed by the RET Proto-Oncogene Mutation
-
Park SY, Jin MJ, Choi EM, Kang SJ, Choi JH, Shim YJ, Kim HS, Jung EY, Lee HJ, Choi MS, Kim HW
- KMID: 2379354
- Clin Pediatr Hematol Oncol.
- 2017 Apr;24(1):75-79.
- doi: 10.15264/cpho.2017.24.1.75
A 9-year-old boy presented with increased sweating and abdominal pain. His mother and uncle had been diagnosed with bilateral pheochromocytoma and medullary thyroid carcinoma. Magnetic resonance imaging of the boy's... -
- CITED
-
- Close
- SHARE
-
- Close
