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Incidental Detection of Parathyroid Adenoma on Somatostatin Receptor PET/CT and Incremental Role of ¹⁸F-Fluorocholine PET/CT in MEN1 Syndrome

Arora S, Damle NA, Passah A, Yadav MP, Ballal S, Aggarwal V, Gupta Y, Kumar P, Tripathi M, Bal C

Multiple endocrine neoplasia type 1 (MEN1) syndrome is characterized by combined occurrence of tumors of endocrine glands including the parathyroid, the pancreatic islet cells, and the anterior pituitary gland. Parathyroid...
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Multiple Endocrine Neoplasia Type 1 Presenting as Hypoglycemia due to Insulinoma

Kwon EB, Jeong HR, Shim YS, Lee HS, Hwang JS

Multiple endocrine neoplasia (MEN) mutation is an autosomal dominant disorder characterized by the occurrence of parathyroid, pancreatic islet, and anterior pituitary tumors. The incidence of insulinoma in MEN is relatively...
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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

Lee DM, Yu SH, Yoon HH, Lee KL, Eom YS, Lee K, Kim BJ, Kim YS, Park IB, Kim KW, Lee S

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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A Case of a Calcitonin-Secreting Pancreatic Endocrine Tumor in a Pateint with Multiple Endocrine Neoplasia Type 1

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 Familial Isolated Primary Hyperparathyroidism with a Novel Gene Mutation

Kim SW, Lee SJ, Kim HS, Kim JY, Jung ED, Jung DS

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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Somatic Mutational Analysis of MEN1 and Phenotypic Correlation in Sporadic Parathyroid Tumors

Chae YS, Kim HJ, Kim SW, Chang MC

PURPOSE: MEN1 gene mutation causes multiple endocrine neoplasia type 1. It also suggests that somatic MEN1 gene mutation plays a role in sporadic endocrine tumor. In this study, we examined...
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A Case of Familial Multiple Endocrine Neoplasia Type 1 with MEN1 Gene Mutation

Jo YE, Choi YJ, Kim YK, Ahn SM, Jung SH, Kim HJ, Kim DJ, Lee KW, Hong JH, Jeong SY, Kim HJ, Chung YS

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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A Case of Familial Multiple Endocrine Neoplasia with MEN1 Gene Mutation

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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