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- W2210912624 abstract "Multiple endocrine neoplasia (MEN), characterized by the occurrence of tumors involving two or more endocrine glands, is broken down into two major forms, MEN1 and MEN2, based on the location of the tumors ( (1) Editorial: Multiple endocrine neoplasia—syndromes of the twentieth century. J Clin Endocrinol Metab. 1998; 83 (2617–20) Google Scholar ). Tumors, both benign and malignant, specific to MEN1, invade the parathyroid glands, pancreatic islet cells, and/or pituitary glands ( (1) Editorial: Multiple endocrine neoplasia—syndromes of the twentieth century. J Clin Endocrinol Metab. 1998; 83 (2617–20) Google Scholar , (2) Carty S.E Helm A.K Amico J.A Clarke M.R Foley T.P Watson C.G Mulvihill J.J The variable penetrance and spectrum of manifestations of multiple endocrine neoplasia type 1. Surgery. 1998; 124: 1106-1114 Google Scholar , (3) Marx S Spiegel A.M Skarulis M.C Doppman J.L Collins F.S Liotta L.A Multiple endocrine neoplasia type I clinical and genetic topics. Ann Int Med. 1998; 129: 484-494 Google Scholar ). MEN2 tumors include medullary carcinoma of the thyroid, pheochromocytoma, and parathyroid adenoma or hyperplasia ( (4) Macdonald J.S Haller D Mc Dougall I.R Weigel R.J Endocrine system. in: Abeloff M.D Armitage J.O Lichter A.S Niederhuber J.E Clinical Oncology. 2nd ed. Churchill Livingstone, New York2000: 1378-1397 Google Scholar ). MEN2 is further specified into MEN2a and MEN2b, with the presence of mucosal neuromas specific to MEN2b ( (4) Macdonald J.S Haller D Mc Dougall I.R Weigel R.J Endocrine system. in: Abeloff M.D Armitage J.O Lichter A.S Niederhuber J.E Clinical Oncology. 2nd ed. Churchill Livingstone, New York2000: 1378-1397 Google Scholar )." @default.
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- W2210912624 title "Case Problem" @default.
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- W2210912624 doi "https://doi.org/10.1016/s0002-8223(01)00357-1" @default.
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