- Imaging Finding of Multiple Endocrine Neoplasia Type 1: Case Report
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Yum TJ, Cho HW
- KMID: 1427220
- J Korean Soc Ultrasound Med.
- 2012 Dec;31(4):247-249.
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant inherited syndrome with characteristic clinical and radiological manifestations. Many reports on MEN1 have been published; however, no cases of radiologically... -
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- Multiple Endocrine Neoplasia and Familial Medullary Thyroid Carcinoma
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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... -
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- A Case of Multiple Endocrine Neoplasia Type I with Atypical Clinical Course
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Choi YS, Bai YS, Ku BJ, Jo YS, Kim YK, Ro HK, Shong M
- KMID: 2333264
- J Korean Endocr Soc.
- 2008 Aug;23(4):266-271.
Multiple endocrine neoplasia type 1 (MEN 1) is characterized by the combined occurrence of primary hyperparathyroidism, enteropancreatic tumors and anterior pituitary adenoma. Yet carcinoid tumors, adrenal adenoma and lipoma might... -
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- A Case of Familial Multiple Endocrine Neoplasia with MEN1 Gene Mutation
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Sung HY, Chun YJ, Lee H, Kwon BJ, Park KW, Lee JM, Moon SD, Chang SA, Han JH
- KMID: 2391913
- J Korean Endocr Soc.
- 2006 Dec;21(6):560-566.
Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal dominant disorder that's characterized by the combined occurrence of primary hyperparathyroidism, endocrine pancreatic tumors and anterior pituitary adenomas, but such... -
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- 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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- Endoscopic Ultrasonography-Guided Ethanol Injection for a Pancreatic Neuroendocrine Tumor with Multiple Endocrine Neoplasia Type 1
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An S, Lee JY, Hwang SH, Park DH, Lee SK
- KMID: 2448580
- Korean J Pancreas Biliary Tract.
- 2016 Oct;21(4):202-208.
- doi: 10.15279/kpba.2016.21.4.202
Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited disorder caused by mutations in the MEN1 gene on chromosome 1. Clinical diagnostic criteria for MEN1 include the presence of... -
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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 Asymptomatic Multiple Endocrine Neoplasia Type 1 Detected Incidentally on Health Screening
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Cho PS, Park H, Lee GH, Lee MC
- KMID: 2277363
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2012 Jun;55(6):373-377.
- doi: 10.3342/kjorl-hns.2012.55.6.373
Multiple endocrine neoplasia type 1 (MEN 1) is characterized by the coexistence of primary hyperparathyroidism, enteropancreatic tumors, and anterior pituitary adenoma. Also adrenal adenoma, lipoma, carcinoid tumors could exist simultaneously... -
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- Neuroendocrine Tumor in Upper Gastrointestinal Tract
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Jeon HK, Kim HS
- KMID: 2249540
- Korean J Helicobacter Up Gastrointest Res.
- 2011 Sep;11(2):75-81.
- doi: 10.7704/kjhugr.2011.11.2.75
Gastric neuroendocrine tumor (GNET) is rare, but increasing in incidence. GNET may be classified into three types on the basis of the background pathology. Type I GNET is related to... -
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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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- A Case of Familial Multiple Endocrine Neoplasia Type 1 with MEN1 Gene Mutation
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Jo YE, Choi YJ, Kim YK, Ahn SM, Jung SH, Kim HJ, Kim DJ, Lee KW, Hong JH, Jeong SY, Kim HJ, Chung YS
- KMID: 2178245
- J Korean Endocr Soc.
- 2007 Feb;22(1):68-73.
- doi: 10.3803/jkes.2007.22.1.68
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the combined occurrence of parathyroid, pancreatic islet and pituitary gland tumors. It is caused by mutation 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 a Calcitonin-Secreting Pancreatic Endocrine Tumor in a Pateint with Multiple Endocrine Neoplasia Type 1
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Choi JH, Kim HI, Kang SM, Kim SG, Oh HK, Bae SH, Ryoo HM
- KMID: 2264796
- Korean J Med.
- 2012 Dec;83(6):817-822.
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant hereditary disorder characterized by the combined occurrence of tumors of the parathyroid gland, exocrine pancreas, and anterior pituitary gland. Calcitonin-secreting... -
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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 Case of Multiple Endocrine Neoplasia Type 1 in Type 2 Diabetes Mellitus with Poor Glycemic Control
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Lee YH, Lee YC, Lee JE, Lee SJ, Jeong SJ, Kim CH
- KMID: 2385575
- J Korean Diabetes.
- 2017 Jun;18(2):125-133.
- doi: 10.4093/jkd.2017.18.2.125
The primary causes of uncontrolled diabetes are poor life-style, infection, ischemic heart disease and inappropriate usage of oral anti-diabetic agents and insulin. Supplementary causes are stroke, acute pancreatitis and endocrine... -
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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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- Multiple endocrine neoplasia type 1 with anterior mediastinal parathyroid adenoma: successful localization using Tc-99m sestamibi SPECT/CT
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Park HL, Yoo IR, Kim SH, Lee S
- KMID: 2360393
- Ann Surg Treat Res.
- 2016 Dec;91(6):323-326.
- doi: 10.4174/astr.2016.91.6.323
The most common manifestation of multiple endocrine neoplasia type 1 (MEN1) is hyperparathyroidism. Treatment of hyperparathyroidism in MEN patients is surgical removal of the parathyroid glands, however ectopic parathyroid gland... -
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