메뉴 건너뛰기




Volumn 34, Issue 2, 2009, Pages 123-135

Adrenal cortical tumors and multiple endocrine neoplasia-related syndromes

Author keywords

Adrenal gland neoplasms; Aldosterone; Hypertension; Multiple endocrine neoplasia

Indexed keywords

CISPLATIN; DOXORUBICIN; ERLOTINIB; ETOPOSIDE; GEFITINIB; GEMCITABINE; METHIONINE; MITOTANE; STREPTOZOCIN; SUNITINIB; TARIQUIDAR;

EID: 70349758565     PISSN: 03911977     EISSN: 18271634     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (6)

References (101)
  • 1
    • 35448973741 scopus 로고    scopus 로고
    • Genetics of adrenal tumors associated with Cushing's syndrome: A new classification for bilateral adrenocortical hyperplasias
    • Stratakis CA, Boikos SA. Genetics of adrenal tumors associated with Cushing's syndrome: a new classification for bilateral adrenocortical hyperplasias. Nat Clin Pract Endocrinol Metab 2007;3:748-57.
    • (2007) Nat Clin Pract Endocrinol Metab , vol.3 , pp. 748-757
    • Stratakis, C.A.1    Boikos, S.A.2
  • 3
    • 29444454897 scopus 로고    scopus 로고
    • Adrenocorticotropic hormone-mediated signaling cascades coordinate a cyclic pattern of steroidogenic factor 1-dependent transcriptional activation
    • Winnay JN, Hammer GD. Adrenocorticotropic hormone-mediated signaling cascades coordinate a cyclic pattern of steroidogenic factor 1-dependent transcriptional activation. Mol Endocrinol 2006;20:147-66.
    • (2006) Mol Endocrinol , vol.20 , pp. 147-166
    • Winnay, J.N.1    Hammer, G.D.2
  • 5
    • 8844257307 scopus 로고    scopus 로고
    • Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
    • Forest MG. Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Hum Reprod Update 2004;10:469-85.
    • (2004) Hum Reprod Update , vol.10 , pp. 469-485
    • Forest, M.G.1
  • 6
    • 75549109638 scopus 로고
    • Congenital adrenocortical hyperplasia with Cushing's syndrome
    • O'Bryan RM, Smith RW Jr, Fine G, Mellinger RC. Congenital adrenocortical hyperplasia with Cushing's syndrome. JAMA 1964;187:257-61.
    • (1964) JAMA , vol.187 , pp. 257-261
    • O'Bryan, R.M.1    Smith Jr., R.W.2    Fine, G.3    Mellinger, R.C.4
  • 7
    • 0034454269 scopus 로고    scopus 로고
    • Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
    • White PC, Speiser PW. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Endocr Rev 2000;21:245-91.
    • (2000) Endocr Rev , vol.21 , pp. 245-291
    • White, P.C.1    Speiser, P.W.2
  • 8
    • 17744365980 scopus 로고    scopus 로고
    • An update of congenital adrenal hyperplasia
    • New MI. An update of congenital adrenal hyperplasia. Ann N Y Acad Sci 2004;1038:14-43
    • (2004) Ann N Y Acad Sci , vol.1038 , pp. 14-43
    • New, M.I.1
  • 9
    • 20444462824 scopus 로고    scopus 로고
    • Congenital adrenal hyperplasia
    • Merke DP, Bornstein SR. Congenital adrenal hyperplasia. Lancet 2005;365:2125-36.
    • (2005) Lancet , vol.365 , pp. 2125-2136
    • Merke, D.P.1    Bornstein, S.R.2
  • 10
    • 0001763647 scopus 로고
    • The adrenogenital syndrome with deficiency of 3beta-hydroxysteroid dehydrogenase
    • Bongiovanni AM. The adrenogenital syndrome with deficiency of 3beta-hydroxysteroid dehydrogenase. J Clin Invest 1962;41:2086.
    • (1962) J Clin Invest , vol.41 , pp. 2086
    • Bongiovanni, A.M.1
  • 11
    • 0026893712 scopus 로고
    • Congenital adrenal hyperplasia due to point mutations in the type II 3beta-hydroxysteroid dehydrogenase gene
    • Rhéaume E, Simard J, Morel Y, Mebarki F, Zachmann M, Forest MG et al. Congenital adrenal hyperplasia due to point mutations in the type II 3beta-hydroxysteroid dehydrogenase gene. Nature Genet 1992;1:239-45.
    • (1992) Nature Genet , vol.1 , pp. 239-245
    • Rhéaume, E.1    Simard, J.2    Morel, Y.3    Mebarki, F.4    Zachmann, M.5    Forest, M.G.6
  • 12
    • 78651056697 scopus 로고
    • Plasma and urinary corticosteroids in the hypertensive form of congenital adrenal hyperplasia
    • Eberlein WR, Bongiovanni AM. Plasma and urinary corticosteroids in the hypertensive form of congenital adrenal hyperplasia. J Biol Chem 1956;223:85-94.
    • (1956) J Biol Chem , vol.223 , pp. 85-94
    • Eberlein, W.R.1    Bongiovanni, A.M.2
  • 14
    • 38049037834 scopus 로고    scopus 로고
    • Basic concepts and recent developments in human steroid hormone biosynthesis
    • Ghayee HK, Auchus RJ. Basic concepts and recent developments in human steroid hormone biosynthesis. Rev Endocr Metab Disord 2007;8:289-300.
    • (2007) Rev Endocr Metab Disord , vol.8 , pp. 289-300
    • Ghayee, H.K.1    Auchus, R.J.2
  • 15
    • 10744224515 scopus 로고    scopus 로고
    • Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome
    • Flück CE, Tajima T, Pandey AV, Arlt W, Okuhara K, Verge CF et al. Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome. Nat Genet 2004;36:228-30.
    • (2004) Nat Genet , vol.36 , pp. 228-230
    • Flück, C.E.1    Tajima, T.2    Pandey, A.V.3    Arlt, W.4    Okuhara, K.5    Verge, C.F.6
  • 16
    • 0022397926 scopus 로고
    • The complex of myxomas, spotty pigmentation, and endocrine overactivity
    • Baltimore
    • Carney JA, Gordon H, Carpenter PC, Shenoy BV, Go VL. The complex of myxomas, spotty pigmentation, and endocrine overactivity. Medicine (Baltimore) 1985;64:270-83.
    • (1985) Medicine , vol.64 , pp. 270-283
    • Carney, J.A.1    Gordon, H.2    Carpenter, P.C.3    Shenoy, B.V.4    Go, V.L.5
  • 17
    • 0032497947 scopus 로고    scopus 로고
    • Identification of a novel genetic locus for familial cardiac myxomas and Carney complex
    • Casey M, Mah C, Merliss AD, Kirschner LS, Taymans SE, Denio AE et al. Identification of a novel genetic locus for familial cardiac myxomas and Carney complex. Circulation 1998;98:2560-6.
    • (1998) Circulation , vol.98 , pp. 2560-2566
    • Casey, M.1    Mah, C.2    Merliss, A.D.3    Kirschner, L.S.4    Taymans, S.E.5    Denio, A.E.6
  • 18
    • 0033812849 scopus 로고    scopus 로고
    • Mutations of the gene encoding the protein kinase a type I- Regulatory subunit in patients with the Carney complex
    • Kirschner LS, Carney JA, Pack SD, Taymans SE, Giatzakis C, Cho YS et al. Mutations of the gene encoding the protein kinase A type I- regulatory subunit in patients with the Carney complex. Nat Genet 2000;26:89-92.
    • (2000) Nat Genet , vol.26 , pp. 89-92
    • Kirschner, L.S.1    Carney, J.A.2    Pack, S.D.3    Taymans, S.E.4    Giatzakis, C.5    Cho, Y.S.6
  • 19
    • 0034853288 scopus 로고    scopus 로고
    • Clinical and molecular features of the Carney complex: Diagnostic criteria and recommendations for patient evaluation
    • Stratakis CA, Kirschner LS, Carney JA. Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation. J Clin Endocrinol Metab 2001;86:4041-6.
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 4041-4046
    • Stratakis, C.A.1    Kirschner, L.S.2    Carney, J.A.3
  • 20
    • 0032697639 scopus 로고    scopus 로고
    • Paradoxical response to dexamethasone in the diagnosis of primary pigmented nodular adrenocortical disease
    • Stratakis CA, Sarlis N, Kirschner LS, Carney JA, Doppman JL, Nieman LK et al. Paradoxical response to dexamethasone in the diagnosis of primary pigmented nodular adrenocortical disease. Ann Intern Med 1999;131:585-91.
    • (1999) Ann Intern Med , vol.131 , pp. 585-591
    • Stratakis, C.A.1    Sarlis, N.2    Kirschner, L.S.3    Carney, J.A.4    Doppman, J.L.5    Nieman, L.K.6
  • 23
    • 39049101528 scopus 로고    scopus 로고
    • Mutation in PDE8B, a cyclic AMP-specific phosphodiesterase in adrenal hyperplasia
    • Horvath A, Mericq V, Stratakis CA Mutation in PDE8B, a cyclic AMP-specific phosphodiesterase in adrenal hyperplasia. N Engl J Med 2008;358:750-2.
    • (2008) N Engl J Med , vol.358 , pp. 750-752
    • Horvath, A.1    Mericq, V.2    Stratakis, C.A.3
  • 25
    • 0026694168 scopus 로고
    • Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome
    • Schwindinger WF, Francomano CA, Levine MA. Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome. Proc Natl Acad Sci USA 1992;89:5152-6.
    • (1992) Proc Natl Acad Sci USA , vol.89 , pp. 5152-5156
    • Schwindinger, W.F.1    Francomano, C.A.2    Levine, M.A.3
  • 27
    • 2442473829 scopus 로고    scopus 로고
    • Activating Gsalpha Mutations: Analysis of 113 Patients with Signs of McCune-Albright Syndrome - A European Collaborative Study
    • DOI 10.1210/jc.2003-031225
    • Lumbroso S, Paris F, Sultan C; European Collaborative Study. Activating Gsalpha mutations: analysis of 113 patients with signs of McCune-Albright syndrome - a European Collaborative Study. J Clin Endocrinol Metab 2004;89:2107-13. (Pubitemid 38619838)
    • (2004) Journal of Clinical Endocrinology and Metabolism , vol.89 , Issue.5 , pp. 2107-2113
    • Lumbroso, S.1    Paris, F.2    Sultan, C.3
  • 28
    • 47349094443 scopus 로고    scopus 로고
    • Collins MT McCune-Albright syndrome
    • Dumitrescu CE, Collins MT McCune-Albright syndrome. Orphanet J Rare Dis 2008;3:12.
    • (2008) Orphanet J Rare Dis , vol.3 , pp. 12
    • Dumitrescu, C.E.1
  • 30
    • 0033504785 scopus 로고    scopus 로고
    • Cushing's syndrome caused by nodular adrenal hyperplasia in children with McCune-Albright syndrome
    • Kirk JM, Brain CE, Carson DJ, Hyde JC, Grant DB. Cushing's syndrome caused by nodular adrenal hyperplasia in children with McCune-Albright syndrome. J Pediatr 1999;134:789-92.
    • (1999) J Pediatr , vol.134 , pp. 789-792
    • Kirk, J.M.1    Brain, C.E.2    Carson, D.J.3    Hyde, J.C.4    Grant, D.B.5
  • 31
    • 19944434190 scopus 로고    scopus 로고
    • An instrument to measure skeletal burden and predict functional outcome in fibrous dysplasia of bone
    • Collins MT, Kushner H, Reynolds JC, Chebli C, Kelly MH, Gupta A et al. An instrument to measure skeletal burden and predict functional outcome in fibrous dysplasia of bone. J Bone Miner Res 2005;20:219-26.
    • (2005) J Bone Miner Res , vol.20 , pp. 219-226
    • Collins, M.T.1    Kushner, H.2    Reynolds, J.C.3    Chebli, C.4    Kelly, M.H.5    Gupta, A.6
  • 33
    • 66849137159 scopus 로고    scopus 로고
    • Rare germline mutations in cyclin-dependent kinase inhibitor genes in MEN1 and related states
    • Epub ahead of print
    • Agarwal SK, Mateo CM, Marx SJ. Rare germline mutations in cyclin-dependent kinase inhibitor genes in MEN1 and related states. J Clin Endocrinol Metab 2009 [Epub ahead of print].
    • (2009) J Clin Endocrinol Metab
    • Agarwal, S.K.1    Mateo, C.M.2    Marx, S.J.3
  • 35
  • 37
    • 13444304438 scopus 로고    scopus 로고
    • Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing
    • Ellard S, Hattersley AT, Brewer CM, Vaidya B. Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing. Clin Endocrinol 2005;62:169-75.
    • (2005) Clin Endocrinol , vol.62 , pp. 169-175
    • Ellard, S.1    Hattersley, A.T.2    Brewer, C.M.3    Vaidya, B.4
  • 38
    • 0000152065 scopus 로고
    • Un cas de polypose adénomateuse: Generalisé e à tout l'intestin
    • Devic A, Bussy MM. Un cas de polypose adénomateuse: Generalisé e à tout l'intestin. Arch Mal Appar Dig 1912; 6:278-89.
    • (1912) Arch Mal Appar Dig , vol.6 , pp. 278-289
    • Devic, A.1    Bussy, M.M.2
  • 39
    • 0001126259 scopus 로고
    • A genetic and clinical study of intestinal polyposis, a predisposing factor for carcinoma of the colon and rectum
    • Gardner EJ. A genetic and clinical study of intestinal polyposis, a predisposing factor for carcinoma of the colon and rectum. Am J Hum Genet 1951;3:167-76.
    • (1951) Am J Hum Genet , vol.3 , pp. 167-176
    • Gardner, E.J.1
  • 40
    • 0026704103 scopus 로고
    • Loss of normal allele of the APC gene in an adrenocortical carcinoma from a patient with familial adenomatous polyposis
    • Seki M, Tanaka K, Kikuchi-Yanoshita R, Konishi M, Fukunari H et al. Loss of normal allele of the APC gene in an adrenocortical carcinoma from a patient with familial adenomatous polyposis. Hum Genet 1992;89:298-300.
    • (1992) Hum Genet , vol.89 , pp. 298-300
    • Seki, M.1    Tanaka, K.2    Kikuchi-Yanoshita, R.3    Konishi, M.4    Fukunari, H.5
  • 41
    • 0031201028 scopus 로고    scopus 로고
    • Adrenocorticotropin-independent macronodular adrenocortical hyperplasia associated with multiple colon adenomas/carcinomas which showed a point mutation in the APC gene
    • Yamakita N, Murai T, Ito Y, Miura K, Ikeda T, Miyamoto K et al. Adrenocorticotropin-independent macronodular adrenocortical hyperplasia associated with multiple colon adenomas/carcinomas which showed a point mutation in the APC gene. Intern Med 1997;36:536-42.
    • (1997) Intern Med , vol.36 , pp. 536-542
    • Yamakita, N.1    Murai, T.2    Ito, Y.3    Miura, K.4    Ikeda, T.5    Miyamoto, K.6
  • 42
    • 0032933125 scopus 로고    scopus 로고
    • Familial adenomatous polyposis associated with multiple adrenal adenomas in a patient with a rare 3′ APC mutation
    • Kartheuser A, Walon C, West S, Breukel C, Detry R, Gribomont AC, et al. Familial adenomatous polyposis associated with multiple adrenal adenomas in a patient with a rare 3′ APC mutation. J Med Genet 1999;36:65-7.
    • (1999) J Med Genet , vol.36 , pp. 65-67
    • Kartheuser, A.1    Walon, C.2    West, S.3    Breukel, C.4    Detry, R.5    Gribomont, A.C.6
  • 44
    • 0034082446 scopus 로고    scopus 로고
    • Primary aldosteronism in a patient with familial adenomatous polyposis
    • Alexander GL, Thompson GB, Schwartz DA. Primary aldosteronism in a patient with familial adenomatous polyposis. Mayo Clin Proc 2000; 75:636-7.
    • (2000) Mayo Clin Proc , vol.75 , pp. 636-637
    • Alexander, G.L.1    Thompson, G.B.2    Schwartz, D.A.3
  • 47
    • 1942436088 scopus 로고    scopus 로고
    • The clinically inapparent adrenal mass: Update in diagnosis and management
    • DOI 10.1210/er.2002-0031
    • Mansmann G, Lau J, Balk E, Rothberg M, Miyachi Y, Bornstein SR. The clinically inapparent adrenal mass: update in diagnosis and management. Endocr Rev 2004;25:309-40. (Pubitemid 38528713)
    • (2004) Endocrine Reviews , vol.25 , Issue.2 , pp. 309-340
    • Mansmann, G.1    Lau, J.2    Balk, E.3    Rothberg, M.4    Miyachi, Y.5    Bornstein, S.R.6
  • 49
    • 33845593204 scopus 로고    scopus 로고
    • Recognizing genes differentially regulated in vitro by the multiple endocrine neoplasia type 1 (MEN1) gene, using RNA interference and oligonucleotide microarrays
    • DOI 10.1016/j.surg.2006.06.038, PII S0039606006004946
    • Stilberg P, Santesson M, Ekeblad S, Lejonklou MH, Skogseid B. Recognizing genes differentially regulated in vitro by the multiple endocrine neoplasia type 1 (MEN1) gene, using RNA interference and oligonucleotide microarrays. Surgery 2006;140:921-31. (Pubitemid 44937376)
    • (2006) Surgery , vol.140 , Issue.6 , pp. 921-931
    • Stalberg, P.1    Santesson, M.2    Ekeblad, S.3    Lejonklou, M.H.4    Skogseid, B.5
  • 51
    • 33750612114 scopus 로고    scopus 로고
    • Mechanisms of disease: Adrenocortical tumors - Molecular advances and clinical perspectives
    • DOI 10.1038/ncpendmet0321, PII NCPENDMET0321
    • Bertherat J, Groussin L, Bertagna X Mechanisms of disease: adrenocortical tumors - molecular advances and clinical perspectives. Nat Clin Pract Endocrinol Metab 2006;2:632-41. (Pubitemid 44691299)
    • (2006) Nature Clinical Practice Endocrinology and Metabolism , vol.2 , Issue.11 , pp. 632-641
    • Bertherat, J.1    Groussin, L.2    Bertagna, X.3
  • 52
  • 54
    • 49649127949 scopus 로고    scopus 로고
    • Detection of somatic beta-catenin mutations in primary pigmented nodular adrenocortical disease (PPNAD)
    • Tadjine M, Lampron A, Ouadi L, Horvath A, Stratakis CA, Bourdeau I. Detection of somatic beta-catenin mutations in primary pigmented nodular adrenocortical disease (PPNAD). Clin Endocrinol 2008;69:367-73.
    • (2008) Clin Endocrinol , vol.69 , pp. 367-373
    • Tadjine, M.1    Lampron, A.2    Ouadi, L.3    Horvath, A.4    Stratakis, C.A.5    Bourdeau, I.6
  • 55
    • 65949092330 scopus 로고    scopus 로고
    • MicroRNA signature of primary pigmented nodular adrenocortical disease: Clinical correlations and regulation of Wnt signaling
    • Iliopoulos D, Bimpaki EI, Nesterova M, Stratakis CA. MicroRNA signature of primary pigmented nodular adrenocortical disease: clinical correlations and regulation of Wnt signaling. Cancer Res 2009;69:3278-82.
    • (2009) Cancer Res , vol.69 , pp. 3278-3282
    • Iliopoulos, D.1    Bimpaki, E.I.2    Nesterova, M.3    Stratakis, C.A.4
  • 56
    • 0014029230 scopus 로고
    • Hypertension, increased aldosterone secretion and low plasma renin activity relieved by dexamethasone
    • Sutherland DJ, Ruse JL, Laidlaw JC. Hypertension, increased aldosterone secretion and low plasma renin activity relieved by dexamethasone. Can Med Assoc J 1966;95:1109-19.
    • (1966) Can Med Assoc J , vol.95 , pp. 1109-1119
    • Sutherland, D.J.1    Ruse, J.L.2    Laidlaw, J.C.3
  • 57
    • 0026580019 scopus 로고
    • A chimaeric 11beta-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension
    • Lifton RP, Dluhy RG, Powers M, Rich GM, Cook S, Ulick S, Lalouel JM. A chimaeric 11beta-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension. Nature 1992;355:262-5.
    • (1992) Nature , vol.355 , pp. 262-265
    • Lifton, R.P.1    Dluhy, R.G.2    Powers, M.3    Rich, G.M.4    Cook, S.5    Ulick, S.6    Lalouel, J.M.7
  • 59
    • 0028890480 scopus 로고
    • A new genetic test for familial hyperaldosteronism type I aids in the detection of curable hypertension
    • Jonsson JR, Klemm SA, Tunny TJ, Stowasser M, Gordon RD. A new genetic test for familial hyperaldosteronism type I aids in the detection of curable hypertension. Biochem Biophys Res Commun 1995;207:565-71.
    • (1995) Biochem Biophys Res Commun , vol.207 , pp. 565-571
    • Jonsson, J.R.1    Klemm, S.A.2    Tunny, T.J.3    Stowasser, M.4    Gordon, R.D.5
  • 61
    • 51749083776 scopus 로고    scopus 로고
    • Case detection, diagnosis, and treatment of patients with primary aldosteronism: An endocrine society clinical practice guideline
    • for the Endocrine Society
    • Funder JW, Carey RM, Fardella C, Gomez-Sanchez CE, Mantero F, Stowasser M et al. for the Endocrine Society. Case detection, diagnosis, and treatment of patients with primary aldosteronism: an endocrine society clinical practice guideline. J Clin Endocrinol Metab 2008;93:3266-81.
    • (2008) J Clin Endocrinol Metab , vol.93 , pp. 3266-3281
    • Funder, J.W.1    Carey, R.M.2    Fardella, C.3    Gomez-Sanchez, C.E.4    Mantero, F.5    Stowasser, M.6
  • 62
    • 0028818948 scopus 로고
    • Primary aldosteronism
    • Gordon RD. Primary aldosteronism. J Endocrinol Invest 1995;18:495-511.
    • (1995) J Endocrinol Invest , vol.18 , pp. 495-511
    • Gordon, R.D.1
  • 65
    • 0003754609 scopus 로고    scopus 로고
    • Extreme cytomegaly of the adrenal fetal cortex, omphalocele, hyperplasia of kidneys and pancreas, and Leydig-cell hyperplasia: Another syndrome?
    • Beckwith JB Extreme cytomegaly of the adrenal fetal cortex, omphalocele, hyperplasia of kidneys and pancreas, and Leydig-cell hyperplasia: another syndrome? 11th Annual Meeting of Western Society for Pediatric Research, Los Angeles 1963.
    • 11th Annual Meeting of Western Society for Pediatric Research, Los Angeles 1963
    • Beckwith, J.B.1
  • 66
    • 76549164702 scopus 로고
    • Familial malformation complex with umbilical hernia and macroglossia - A new syndrome?
    • Wiedemann HR. Familial malformation complex with umbilical hernia and macroglossia - a new syndrome? J Genet Hum 1964;13:223-32.
    • (1964) J Genet Hum , vol.13 , pp. 223-232
    • Wiedemann, H.R.1
  • 67
    • 0021330987 scopus 로고
    • A case of Beckwith-Wiedemann syndrome with conductive hearing loss
    • Daugbjerg P, Everberg G. A case of Beckwith-Wiedemann syndrome with conductive hearing loss. Acta Paediatr Scand 1984;73:408-10.
    • (1984) Acta Paediatr Scand , vol.73 , pp. 408-410
    • Daugbjerg, P.1    Everberg, G.2
  • 69
    • 23944520114 scopus 로고    scopus 로고
    • Beckwith-Wiedemann syndrome: Historical, clinicopathological, and etiopathogenetic perspectives
    • Cohen MM Jr. Beckwith-Wiedemann syndrome: historical, clinicopathological, and etiopathogenetic perspectives. Pediatr Dev Pathol 2005;8:287-304.
    • (2005) Pediatr Dev Pathol , vol.8 , pp. 287-304
    • Cohen Jr., M.M.1
  • 73
    • 3142726223 scopus 로고    scopus 로고
    • Role of the insulin-like growth factor system in adrenocortical growth control and carcinogenesis
    • DOI 10.1055/s-2004-814563
    • Fottner Ch, Hoeflich A, Wolf E, Weber MM. Role of the insulin-like growth factor system in adrenocortical growth control and carcinogenesis. Horm Metab Res 2004;36:397-405. (Pubitemid 38932097)
    • (2004) Hormone and Metabolic Research , vol.36 , Issue.6 , pp. 397-405
    • Fottner, Ch.1    Hoeflich, A.2    Wolf, E.3    Weber, M.M.4
  • 74
    • 0036298023 scopus 로고    scopus 로고
    • Signaling pathways in adrenocortical cancer
    • Kirschner LS. Signaling pathways in adrenocortical cancer. Ann NY Acad Sci 2002;968:222-39.
    • (2002) Ann NY Acad Sci , vol.968 , pp. 222-239
    • Kirschner, L.S.1
  • 76
    • 47149106025 scopus 로고    scopus 로고
    • Beckwith-Wiedemann syndrome in adults: Observations from one family and recommendations for care
    • DOI 10.1002/ajmg.a.32332
    • Greer KJ, Kirkpatrick SJ, Weksberg R, Pauli RM. Beckwith-Wiedemann syndrome in adults: observations from one family and recommendations for care. Am J Med Genet A 2008;146A:1707-12. (Pubitemid 351975481)
    • (2008) American Journal of Medical Genetics, Part a , vol.146 , Issue.13 , pp. 1707-1712
    • Greer, K.J.1    Kirkpatrick, S.J.2    Weksberg, R.3    Pauli, R.M.4
  • 77
    • 33747437581 scopus 로고    scopus 로고
    • Tumour surveillance in Beckwith-Wiedemann syndrome and hemihyperplasia a critical review of the evidence and suggested guidelines for local practice
    • Tan TY, Amor DJ. Tumour surveillance in Beckwith-Wiedemann syndrome and hemihyperplasia: a critical review of the evidence and suggested guidelines for local practice. J Paediatr Child Health 2006;42:486-90.
    • (2006) J Paediatr Child Health , vol.42 , pp. 486-490
    • Tan, T.Y.1    Amor, D.J.2
  • 79
    • 0028220688 scopus 로고
    • Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families
    • Birch JM, Hartley AL, Tricker KJ, Prosser J, Condie A, Kelsey AM et al. Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families. Cancer Res 1994;54:1298-304.
    • (1994) Cancer Res , vol.54 , pp. 1298-1304
    • Birch, J.M.1    Hartley, A.L.2    Tricker, K.J.3    Prosser, J.4    Condie, A.5    Kelsey, A.M.6
  • 81
    • 19944433455 scopus 로고    scopus 로고
    • Genetic mapping of a third Li-Fraumeni syndrome predisposition locus to human chromosome 1q23
    • Bachinski LL, Olufemi SE, Zhou X, Wu CC, Yip L, Shete S et al. Genetic mapping of a third Li-Fraumeni syndrome predisposition locus to human chromosome 1q23. Cancer Res 2005;65:427-31.
    • (2005) Cancer Res , vol.65 , pp. 427-431
    • Bachinski, L.L.1    Olufemi, S.E.2    Zhou, X.3    Wu, C.C.4    Yip, L.5    Shete, S.6
  • 82
    • 0033709244 scopus 로고    scopus 로고
    • Characterization of indeterminate (lipid-poor) adrenal masses: Use of washout characteristics at contrast-enhanced CT
    • Peña CS, Boland GW, Hahn PF, Lee MJ, Mueller PR. Characterization of indeterminate (lipid-poor) adrenal masses: use of washout characteristics at contrast-enhanced CT. Radiology 2000;217:798-802.
    • (2000) Radiology , vol.217 , pp. 798-802
    • Peña, C.S.1    Boland, G.W.2    Hahn, P.F.3    Lee, M.J.4    Mueller, P.R.5
  • 83
    • 58149200067 scopus 로고    scopus 로고
    • Incidental adrenal lesions: Principles, techniques, and algorithms for imaging characterization
    • Boland GW, Blake MA, Hahn PF, Mayo-Smith WW. Incidental adrenal lesions: principles, techniques, and algorithms for imaging characterization. Radiology 2008;249:756-75.
    • (2008) Radiology , vol.249 , pp. 756-775
    • Boland, G.W.1    Blake, M.A.2    Hahn, P.F.3    Mayo-Smith, W.W.4
  • 85
    • 47549111741 scopus 로고    scopus 로고
    • Improved detection of hepatic metastases of adrenocortical cancer by contrast-enhanced ultrasound
    • Bauditz J, Quinkler M, Beyersdorff D, Wermke W. Improved detection of hepatic metastases of adrenocortical cancer by contrast-enhanced ultrasound. Oncol Rep 2008;19:1135-9.
    • (2008) Oncol Rep , vol.19 , pp. 1135-1139
    • Bauditz, J.1    Quinkler, M.2    Beyersdorff, D.3    Wermke, W.4
  • 90
    • 33751529232 scopus 로고    scopus 로고
    • Efficacy of adjuvant radiotherapy of the tumor bed on local recurrence of adrenocortical carcinoma
    • Fassnacht M, Hahner S, Polat B, Koschker AC, Kenn W, Flentje M et al. Efficacy of adjuvant radiotherapy of the tumor bed on local recurrence of adrenocortical carcinoma. J Clin Endocrinol Metab 2006;91:4501-4.
    • (2006) J Clin Endocrinol Metab , vol.91 , pp. 4501-4504
    • Fassnacht, M.1    Hahner, S.2    Polat, B.3    Koschker, A.C.4    Kenn, W.5    Flentje, M.6
  • 92
    • 58549084169 scopus 로고    scopus 로고
    • Adrenocortical cancer treatment
    • Patalano A, Brancato V, Mantero F. Adrenocortical cancer treatment. Horm Res 2009;71(Suppl 1):99-104.
    • (2009) Horm Res , vol.71 , Issue.SUPPL. 1 , pp. 99-104
    • Patalano, A.1    Brancato, V.2    Mantero, F.3
  • 93
    • 33744952176 scopus 로고    scopus 로고
    • Clinical review: Adrenocortical carcinoma clinical update
    • Allolio B, Fassnacht M. Clinical review: Adrenocortical carcinoma: clinical update. J Clin Endocrinol Metab 2006;91:2027-37.
    • (2006) J Clin Endocrinol Metab , vol.91 , pp. 2027-2037
    • Allolio, B.1    Fassnacht, M.2
  • 96
    • 59449084843 scopus 로고    scopus 로고
    • Limited prognostic value of the 2004 International Union Against Cancer staging classification for adrenocortical carcinoma: Proposal for a revised TNM classification
    • for the German Adrenocortical Carcinoma Registry Group; European Network for the Study of Adrenal Tumors
    • Fassnacht M, Johanssen S, Quinkler M, Bucsky P, Willenberg HS, Beuschlein F et al. for the German Adrenocortical Carcinoma Registry Group; European Network for the Study of Adrenal Tumors. Limited prognostic value of the 2004 International Union Against Cancer staging classification for adrenocortical carcinoma: proposal for a revised TNM classification. Cancer 2009;115:243-50.
    • (2009) Cancer , vol.115 , pp. 243-250
    • Fassnacht, M.1    Johanssen, S.2    Quinkler, M.3    Bucsky, P.4    Willenberg, H.S.5    Beuschlein, F.6
  • 97
    • 0015240161 scopus 로고
    • Multiple specific hormone receptors in the adenylate cyclase of an adrenocortical carcinoma
    • Schorr I, Rathnam P, Saxena BB, Ney RL. Multiple specific hormone receptors in the adenylate cyclase of an adrenocortical carcinoma. J Biol Chem 1971;246:5806-11.
    • (1971) J Biol Chem , vol.246 , pp. 5806-5811
    • Schorr, I.1    Rathnam, P.2    Saxena, B.B.3    Ney, R.L.4
  • 98
    • 0035118956 scopus 로고    scopus 로고
    • Ectopic and abnormal hormone receptors in adrenal Cushing's syndrome
    • DOI 10.1210/er.22.1.75
    • Lacroix A, N'Diaye N, Tremblay J, Hamet P. Ectopic and abnormal hormone receptors in adrenal Cushing's syndrome. Endocr Rev 2001;22:75-110. (Pubitemid 32187804)
    • (2001) Endocrine Reviews , vol.22 , Issue.1 , pp. 75-110
    • Lacroix, A.1    N'Diaye, N.2    Tremblay, J.3    Hamet, P.4
  • 99
    • 1142273445 scopus 로고    scopus 로고
    • Constitutive activation of the human ACTH receptor resulting from a synergistic interaction between two naturally occurring missense mutations in the MC2R gene
    • Swords FM, Noon LA, King PJ, Clark AJ. Constitutive activation of the human ACTH receptor resulting from a synergistic interaction between two naturally occurring missense mutations in the MC2R gene. Mol Cell Endocrinol 2004;213:149-54.
    • (2004) Mol Cell Endocrinol , vol.213 , pp. 149-154
    • Swords, F.M.1    Noon, L.A.2    King, P.J.3    Clark, A.J.4
  • 100
    • 0036908575 scopus 로고    scopus 로고
    • Impaired desensitization of a mutant adrenocorticotropin receptor associated with apparent constitutive activity
    • Swords FM, Baig A, Malchoff DM, Malchoff CD, Thorner MO, King PJ et al. Impaired desensitization of a mutant adrenocorticotropin receptor associated with apparent constitutive activity. Mol Endocrinol 2002;16:2746-53.
    • (2002) Mol Endocrinol , vol.16 , pp. 2746-2753
    • Swords, F.M.1    Baig, A.2    Malchoff, D.M.3    Malchoff, C.D.4    Thorner, M.O.5    King, P.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.