Primary hyperparathyroidism in multiple endocrine neoplasia type 1: when to perform surgery?

被引:32
作者
Giusti, Francesca [1 ]
Tonelli, Francesco [2 ]
Brandi, Maria Luisa [1 ]
机构
[1] Univ Hosp Careggi, Bone & Mineral Metab Unit, Dept Internal Med, Florence, Italy
[2] Univ Hosp Careggi, Dept Clin Physiopathol, Florence, Italy
关键词
Primary hyperparathyroidism; Multiple endocrine neoplasia 1; PHPT-MEN1; Subtotal parathyroidectomy; Total parathyroidectomy; 1-ASSOCIATED PRIMARY HYPERPARATHYROIDISM; PARATHYROID SURGERY; MEN1; MUTATION; GENE; SEVERITY; DENSITY; PROFILE; TUMORS;
D O I
10.6061/clinics/2012(Sup01)23
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Primary hyperparathyroidism is a common endocrinological disorder. In rare circumstances, it is associated with familial syndromes, such as multiple endocrine neoplasia type 1. This syndrome is caused by a germline mutation in the multiple endocrine neoplasia type 1 gene encoding the tumor-suppressor protein menin. Usually, primary hyperparathyroidism is the initial clinical expression in carriers of multiple endocrine neoplasia type 1 mutations, occurring in more than 90% of patients and appearing at a young age (20-25 years). Multiple endocrine neoplasia type 1/primary hyperparathyroidism is generally accompanied by multiglandular disease, clinically manifesting with hypercalcemia, although it can remain asymptomatic for a long time and consequently not always be recognized early. Surgery is the recommended treatment. The goal of this short review is to discuss the timing of surgery in patients when primary hyperparathyroidism is associated with multiple endocrine neoplasia type 1.
引用
收藏
页码:141 / 144
页数:4
相关论文
共 39 条
[11]   Positional cloning of the gene for multiple endocrine neoplasia-type 1 [J].
Chandrasekharappa, SC ;
Guru, SC ;
Manickam, P ;
Olufemi, SE ;
Collins, FS ;
EmmertBuck, MR ;
Debelenko, LV ;
Zhuang, ZP ;
Lubensky, IA ;
Liotta, LA ;
Crabtree, JS ;
Wang, YP ;
Roe, BA ;
Weisemann, J ;
Boguski, MS ;
Agarwal, SK ;
Kester, MB ;
Kim, YS ;
Heppner, C ;
Dong, QH ;
Spiegel, AM ;
Burns, AL ;
Marx, SJ .
SCIENCE, 1997, 276 (5311) :404-407
[12]   Novel 1113delC menin gene mutation in a Polish family with multiple endocrine neoplasia type 1 syndrome [J].
Chudek, Jerzy ;
Piecha, Grzegorz ;
Nieszporek, Teresa ;
Marini, Francesca ;
Brandi, Maria Luisa ;
Wiecek, Andrzej .
EUROPEAN JOURNAL OF INTERNAL MEDICINE, 2006, 17 (06) :447-449
[13]   Preserved three-dimensional cancellous bone structure in mild primary hyperparathyroidism [J].
Dempster, D. W. ;
Mueller, R. ;
Zhou, H. ;
Kohler, T. ;
Shane, E. ;
Parisien, M. ;
Silverberg, S. J. ;
Bilezikian, J. P. .
BONE, 2007, 41 (01) :19-24
[14]  
Eller-Vainicher C, 2009, J BONE MINER RES, V24, P1404, DOI [10.1359/JBMR.090304, 10.1359/jbmr.090304]
[15]   Effect of treatment with depot somatostatin analogue octreotide on primary hyperparathyroidism (PHP) in multiple endocrine neoplasia type 1 (MEN1) patients [J].
Faggiano, Antongiulio ;
Tavares, Lidice Brandao ;
Tauchmanova, Libuse ;
Milone, Francesco ;
Mansueto, Gelsomina ;
Ramundo, Valeria ;
De Caro, Maria Laura Del Basso ;
Lombardi, Gaetano ;
De Rosa, Gaetano ;
Colao, Annamaria .
CLINICAL ENDOCRINOLOGY, 2008, 69 (05) :756-762
[16]   DNA-based test: when and why to apply it to primary hyperparathyroidism clinical phenotypes [J].
Falchetti, A. ;
Marini, F. ;
Giusti, F. ;
Cavalli, L. ;
Cavalli, T. ;
Brandi, M. L. .
JOURNAL OF INTERNAL MEDICINE, 2009, 266 (01) :69-83
[17]  
Falchetti A, 1997, GENEREVIEWS GENETEST
[18]   A patient with MEN 1-associated hyperparathyroidism, responsive to cinacalcet [J].
Falchetti, Alberto ;
Cilotti, Antonio ;
Vagelli, Luca ;
Masi, Laura ;
Amedei, Antonietta ;
Cioppi, Federica ;
Tonelli, Francesco ;
Brandi, Maria Luisa .
NATURE CLINICAL PRACTICE ENDOCRINOLOGY & METABOLISM, 2008, 4 (06) :351-357
[19]   Multiple endocrine neoplasia type 1 (MEN1): Not only inherited endocrine tumors [J].
Falchetti, Alberto ;
Marini, Francesca ;
Luzi, Ettore ;
Giusti, Francesca ;
Cavalli, Loredana ;
Cavalli, Tiziana ;
Brandi, Maria Luisa .
GENETICS IN MEDICINE, 2009, 11 (12) :825-835
[20]   Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia [J].
Georgitsi, Marianthi ;
Raitila, Anniina ;
Karhu, Auli ;
van der Luijt, Rob B. ;
Aalfs, Cora M. ;
Sane, Timo ;
Vierimaa, Outi ;
Makinen, Markus J. ;
Tuppurainen, Karoliina ;
Paschke, Ralph ;
Gimm, Oliver ;
Koch, Christian A. ;
Gundogdu, Sadi ;
Lucassen, Anneke ;
Tischkowitz, Marc ;
Izatt, Louise ;
Aylwin, Simon ;
Bano, Gul ;
Hodgson, Shirley ;
De Menis, Ernesto ;
Launonen, Virpi ;
Vahteristo, Pia ;
Aaltonen, Lauri A. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2007, 92 (08) :3321-3325