- Multiple Neuroendocrine Tumors in Stomach and Duodenum in a Multiple Endocrine Neoplasia Type 1 Patient
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Kim B, Yang HK, Kim WH
- KMID: 2408514
- J Pathol Transl Med.
- 2018 Mar;52(2):126-129.
- doi: 10.4132/jptm.2017.09.16
A 67-year-old woman with a history of subtotal parathyroidectomy, distal pancreatectomy, and total splenectomy 23 years prior underwent surgical gastric resection for neuroendocrine tumors of the stomach and duodenum. Meticulous... -
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- Hereditary Aspect of Isolated Familial Acromegaly
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Lee WC, Shin MS, Lee KS, Jung N, Huh SK
- KMID: 1694193
- J Korean Neurosurg Soc.
- 1993 Dec;22(12):1309-1318.
Acromegaly is classically considered a sporadic nonfamilial condition. The familial occurance of pituitary adenomas is encountered as a manifestation of the Multiple Endocrine Neoplasia Type I(MEN 1). Moreover in MEN... -
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- Clinical Manifestation of Multiple Endocrine Neoplasia Type I
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Kim YS, Hong SJ
- KMID: 2376124
- Korean J Endocr Surg.
- 2004 Jun;4(1):31-35.
- doi: 10.16956/kjes.2004.4.1.31
PURPOSE: Multiple endocrine neoplasia type I is rarely reported in Korea. The purpose of this study is to analyze the clinical features and the treatment of MEN1 which had been... -
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- A case of multiple endocrine neoplasia type 1 with thymic carcinoid tumor
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Cho M, Lee KM, Song DH, Ahn CW, Kim KR, Hwang JJ, Baek HC
- KMID: 2081157
- Korean J Med.
- 2005 Oct;69(4):428-433.
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant tumor syndrome. Thymic carcinoid tumors in MEN1 are not common and their natural history is little known. But development of... -
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- Multiple Pancreatic Islet Cell Tumors with Diverse Hormonal Expression in a Multiple Endocrine Neoplasia Type I Patient: A Case Report
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Kim JH, Lee KU, Kim WH, Kim YI
- KMID: 1979385
- Korean J Pathol.
- 2002 Jun;36(3):184-186.
Multiple endocrine neoplasia type I is characterized by multiple tumors, particularly in the parathyroid glands, the pituitary gland and the pancreatic islet. We observed multiple pancreatic islet cell tumors with... -
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- Multiple Endocrine Neoplasia Type 1 Presenting with an Invasive Giant Prolactinoma
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Cha J, Kim JS, Han JS, Park YW, Kim MJ, Ku YH, Kim HI
- KMID: 2361438
- Korean J Med.
- 2016 Dec;91(3):300-305.
- doi: 10.3904/kjm.2016.91.3.300
Pituitary tumors occur in 15-50% of patients with multiple endocrine neoplasia of type 1 (MEN1). To the best of our knowledge, no MEN1 case in which the initial lesion was... -
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- A Case of Multiple Endocrine Neoplasia Type 1 Combined with Papillary Thyroid Carcinoma
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Kim HJ, Park JS, Kim CS, Kang ES, Cha BS, Lim SK, Kim KR, Lee HC, Ahn CW
- KMID: 724269
- Yonsei Med J.
- 2008 Jun;49(3):503-506.
- doi: 10.3349/ymj.2008.49.3.503
This is the first report of papillary thyroid carcinoma combined with multiple endocrine neoplasia type 1 (MEN1) in Korea. MEN1 is a hereditary disease comprising neoplastic disorders such as pituitary,... -
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- A Novel Germline Mutation of MEN1 Gene in a Young-aged Multiple Insulinoma with Hyperparathyroidism
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Park YJ
- KMID: 2308577
- Korean J Endocr Surg.
- 2015 Dec;15(4):99-102.
- doi: 10.16956/kaes.2015.15.4.99
Multiple endocrine neoplasia type 1 is an autosomal dominant disease caused by the MEN1 germline mutation. A 25-year-old male was admitted for loss of consciousness. Initial laboratory data showed hypoglycemia... -
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- The Characteristics of Multiple Endocrine Neoplasia in Korean
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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... -
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- A Case of Multiple Endocrine Neoplasia Type 1
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Lee DS, Song MH, Kim W, Park IY, Won JM
- KMID: 2005651
- J Korean Surg Soc.
- 1997 Aug;53(2):287-293.
In 1903 Erdheim reported multiple endocrine neoplasia type 1 (MEN 1) by autopsy, and in 1954 Wermer reported a familial occurrence of multiple tumors which were associated with neoplastic transformation... -
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- Early Symptoms and Clinical Manifestations in Korean Patients with Multiple Endocrine Neoplasia
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Kim KH, Koo MY, Hur SM, Lee SK, Choe JH, Lee JE, Kim JS, Chung JH, Nam SJ, Yang JH, Kim JH
- KMID: 2375481
- Korean J Endocr Surg.
- 2010 Dec;10(4):266-275.
- doi: 10.16956/kjes.2010.10.4.266
PURPOSE: Multiple endocrine neoplasia (MEN) syndrome is an inherited, autosomal dominant disease that presents as a combination of several endocrine tumors. Early diagnosis of this syndrome is difficult, because of... -
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- A Case of Multiple Endocrine Neoplasia Type 1 with Mutation in MENIN Gene
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Park SE, Kang ES, Lee HJ, Kim SH, Do MY, Kang SA, Han SJ, Kim HJ, Ahn CW, Cha BS, Lim SK, Kim KR, Kim IJ, Lee HC
- KMID: 2100455
- J Korean Soc Endocrinol.
- 2005 Feb;20(1):71-77.
- doi: 10.3803/jkes.2005.20.1.71
Multiple endocrine neoplasia type 1(MEN 1) is an autosomal dominantly inherited syndrome, characterized by the combined occurrence of tumors of the parathyroid glands, endocrine pancreas, and anterior pituitary gland. The... -
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- Characteristics of the Germline MEN1 Mutations in Korea: A Literature Review
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Lee SC, Min JW, Kim YM, Chang MC
- KMID: 1709075
- Korean J Endocr Surg.
- 2014 Mar;14(1):7-11.
PURPOSE: Multiple endocrine neoplasia type 1 (MEN-1) is an autosomal dominant disease caused by the MEN1 germline mutation. We reviewed previous reports in order to summarize the characteristics of germline... -
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- Clinical Features of Multiple Endocrine Neoplasia Type I in Koreans
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Kim CH, Kim GS, Kim HK, Park JY, Shong YK, Lee KU
- KMID: 2461618
- J Korean Soc Endocrinol.
- 1996 Jun;11(2):163-174.
Background: Multiple endocrine neoplasia type I(MEN I) is a rare, eomplex, and potentially lethal disease. In Korean, only five anecdotal cases were reported as yet. The authors rescently experienced four... -
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- Pheochromocytoma with pancreatic islet cell tumor: a case report
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Ju YT, Jung EJ, Park SH, Hong SC
- KMID: 2244404
- Korean J Hepatobiliary Pancreat Surg.
- 2000 Feb;4(1):191-195.
A 17-years old woman with a combination of unilateral pheochromocytoma and an asymptomatic islet cell tumor of the pancreas is presented. The unusual coincidence of pheochromocytoma and pancreatic islet cell... -
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- Neuroendocrine Tumors in the Stomach, Duodenum, and Pancreas Accompanied by Novel MEN1 Gene Mutation
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Yang MA, Lee WK, Shin HS, Park SH, Kim BS, Kim JW, Cho JW, Yun SH
- KMID: 2383412
- Korean J Gastroenterol.
- 2017 Mar;69(3):181-186.
- doi: 10.4166/kjg.2017.69.3.181
Multiple endocrine neoplasia type 1 (MEN1) syndrome is a relatively rare disease, characterized by the occurrence of multiple endocrine tumors in the parathyroid and pituitary glands as well as the... -
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- A Case of Multiple Endocrine Neoplasia Type 1 with Papillary Thyroid Carcinoma
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Kim HJ, Kim CS, Je HC, Park J, Park JS, Kong JH, Kang ES, Ahn CW, Cha BS, Lim SK, Kim KR, Lee HC, Jang HS, Hong SW
- KMID: 2200673
- J Korean Soc Endocrinol.
- 2006 Feb;21(1):79-84.
- doi: 10.3803/jkes.2006.21.1.79
This is the first report of papillary thyroid carcinoma combined with multiple endocrine neoplasia type 1 (MEN 1). It is an hereditary syndrome characterized by neoplastic disorders such as pituitary... -
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- A Case of Familial Isolated Primary Hyperparathyroidism with a Novel Gene Mutation
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Kim SW, Lee SJ, Kim HS, Kim JY, Jung ED, Jung DS
- KMID: 1497766
- Endocrinol Metab.
- 2010 Dec;25(4):374-377.
- doi: 10.3803/EnM.2010.25.4.374
Familial isolated primary hyperparathyroidism (FIHP) is an autosomal dominant disorder that is characterized by an early stage of either multiple endocrine neoplasia type 1 (MEN1) or hyperparathyroidism-jaw tumor (HPT-JT) syndrome.... -
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- Genetic Analysis of Multiple Endocrine Neoplasia Type 1 (MEN1) Leads to Misdiagnosis of an Extremely Rare Presentation of Intrasellar Cavernous Hemangioma as MEN1
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Lee DM, Yu SH, Yoon HH, Lee KL, Eom YS, Lee K, Kim BJ, Kim YS, Park IB, Kim KW, Lee S
- KMID: 2169421
- Endocrinol Metab.
- 2014 Jun;29(2):146-153.
- doi: 10.3803/EnM.2014.29.2.146
BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited disorder characterized by the simultaneous occurrence of endocrine tumors in target tissues (mainly the pituitary, endocrine pancreas, and parathyroid... -
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- Genetic and Epigenetic Analysis in Korean Patients with Multiple Endocrine Neoplasia Type 1
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Chung YJ, Hwang S, Jeong JJ, Song SY, Kim SH, Rhee Y
- KMID: 2169463
- Endocrinol Metab.
- 2014 Sep;29(3):270-279.
- doi: 10.3803/EnM.2014.29.3.270
BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a familial syndrome characterized by the parathyroid, pancreas and pituitary tumors. Parathyroid tumors are the most common clinical manifestations, occurring in more... -
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