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Volumn 69, Issue 2 SUPPL.1, 2014, Pages 97-103

Pheochromocytoma: From the bench to the surgery

Author keywords

Operative; Pheochromocytoma; Proto oncogene proteins c ret; Surgical procedures

Indexed keywords


EID: 84907422036     PISSN: 00264733     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (36)
  • 2
    • 0023003129 scopus 로고
    • Pheocromocytoma in Sweden, 1958-81. An analysis of the national cancer registry data
    • Stenstrom G, Svardsudd K Pheocromocytoma in Sweden, 1958-81. An analysis of the National Cancer Registry Data. Acta Med Scand 1986;220:225-32.
    • (1986) Acta Med Scand , vol.220 , pp. 225-232
    • Stenstrom, G.1    Svardsudd, K.2
  • 3
    • 0026719185 scopus 로고
    • Biochemical diagnosis of pheocromocytoma by simultaneous measurement of urinary excretion of epinephrine and norepinephrine
    • Smythe GA, Edwards G, Graham P, Lazarus L. Biochemical diagnosis of pheocromocytoma by simultaneous measurement of urinary excretion of epinephrine and norepinephrine. Clinical chemistry 1992;38:486-92.
    • (1992) Clinical Chemistry , vol.38 , pp. 486-492
    • Smythe, G.A.1    Edwards, G.2    Graham, P.3    Lazarus, L.4
  • 4
    • 84923219942 scopus 로고
    • Hereditary paraganglioma-pheocromocytoma syndromes
    • Pagon RA Bird TD Dolan CR et al. editors. Seattle WA: University of Washington [Internet] [cited 2012; Aug 30]
    • Kirmani S, Young WF. Hereditary paraganglioma-pheocromocytoma syndromes. In: Pagon RA, Bird TD, Dolan CR et al. editors. GeneReviews. Seattle, WA: University of Washington; 1993 [Internet]. Available from: http://www.ncbi.nlm. nih.gov/books/NBK1548 [cited 2012; Aug 30].
    • (1993) GeneReviews
    • Kirmani, S.1    Young, W.F.2
  • 5
    • 0003686128 scopus 로고    scopus 로고
    • Background and importance and diagnosis
    • Manger WM, Gifford RW, editors. 2nd edition. Cambrige: Blackwell Science
    • Manger WM, Gifford RW. Background and importance and diagnosis. In: Manger WM, Gifford RW, editors. Clinical and Experimental pheocromocytoma. 2nd edition. Cambrige: Blackwell Science; 1996. p. 205-332.
    • (1996) Clinical and Experimental Pheocromocytoma , pp. 205-332
    • Manger, W.M.1    Gifford, R.W.2
  • 7
    • 18344380647 scopus 로고    scopus 로고
    • Molecular genetics of multiple endocrine neoplasia types 1
    • Marx SJ. Molecular genetics of multiple endocrine neoplasia types 1. Nat Rev Cancer 2005;5:367-75.
    • (2005) Nat Rev Cancer , vol.5 , pp. 367-375
    • Marx, S.J.1
  • 8
    • 13144258730 scopus 로고    scopus 로고
    • Multiple endocrine neoplasia syndrome: Genetic basis for clinical management
    • Carling T. Multiple endocrine neoplasia syndrome: genetic basis for clinical management. Curr Opin Oncol 2005;17:7-12.
    • (2005) Curr Opin Oncol , vol.17 , pp. 7-12
    • Carling, T.1
  • 10
    • 19944424474 scopus 로고    scopus 로고
    • Multiple endocrine neoplasia type 2
    • Peczkowska M, Januszewicz A. Multiple endocrine neoplasia type 2. Fam Cancer 2005;4:25-36.
    • (2005) Fam Cancer , vol.4 , pp. 25-36
    • Peczkowska, M.1    Januszewicz, A.2
  • 11
    • 0029131324 scopus 로고
    • Activated RET/PTC oncogene elicits immediate early and delayed response genes in PC12 cells
    • Califano D, Monaco C, de Vita G, D'Alessio A, Dathan NA, Possenti R et al. Activated RET/PTC oncogene elicits immediate early and delayed response genes in PC12 cells. Oncogene 1995;11:107-12.
    • (1995) Oncogene , vol.11 , pp. 107-112
    • Califano, D.1    Monaco, C.2    De Vita, G.3    D'alessio, A.4    Dathan, N.A.5    Possenti, R.6
  • 12
    • 0033304922 scopus 로고    scopus 로고
    • A novel case of multiple endocrine neoplasia type 2A associated with three de novo mutations of the RET protooncogene
    • Tessitore A, Sinisi AA, Pasquali D, Cardone M, Vitale D, Bellastella A et al. A novel case of multiple endocrine neoplasia type 2A associated with three de novo mutations of the RET protooncogene. J Clin Endocrinol Metab 1999;10:3522-7.
    • (1999) J Clin Endocrinol Metab , vol.10 , pp. 3522-3527
    • Tessitore, A.1    Sinisi, A.A.2    Pasquali, D.3    Cardone, M.4    Vitale, D.5    Bellastella, A.6
  • 14
    • 29144484161 scopus 로고    scopus 로고
    • The SDH mutation database: An online resource for succinate dehydrogenase sequence variants involved in pheocromocytoma, paraganglioma and mitochondrial complex II deficiency
    • Bayley JP, Devilee P, Taschner PE. The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheocromocytoma, paraganglioma and mitochondrial complex II deficiency. BMC Med Genet 2005;6:39.
    • (2005) BMC Med Genet , vol.6 , pp. 39
    • Bayley, J.P.1    Devilee, P.2    Taschner, P.E.3
  • 15
    • 84860247039 scopus 로고    scopus 로고
    • Pheocromocytoma and paraganglioma: Understanding the complexities of the genetic background
    • Fishbein L, Nathanson KL. Pheocromocytoma and paraganglioma: understanding the complexities of the genetic background. Cancer Genet 2012;205:1-11.
    • (2012) Cancer Genet , vol.205 , pp. 1-11
    • Fishbein, L.1    Nathanson, K.L.2
  • 16
    • 66849143816 scopus 로고    scopus 로고
    • SDH mutations in tumorigenesis and inherited endocrine tumours: Lesson from the phaeochromocytoma-paraganglioma syndromes
    • Pasini B, Stratakis CA. SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma-paraganglioma syndromes. J Intern Med 2009;266:19-42.
    • (2009) J Intern Med , vol.266 , pp. 19-42
    • Pasini, B.1    Stratakis, C.A.2
  • 18
    • 0037364314 scopus 로고    scopus 로고
    • A role of mitochondrial enzymes in inherited neoplasia and beyond
    • Eng C, Kiuru M, Fernandez MJ, Aaltonen LA. A role of mitochondrial enzymes in inherited neoplasia and beyond. Nat Rev Cancer 2003;3:193-202.
    • (2003) Nat Rev Cancer , vol.3 , pp. 193-202
    • Eng, C.1    Kiuru, M.2    Fernandez, M.J.3    Aaltonen, L.A.4
  • 19
    • 4143105824 scopus 로고    scopus 로고
    • Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations
    • Neumann HP, Pawlu C, Peczkowska M, Bausch B, McWhinney SR, Muresan M et al. Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. Jama 2004;292:943-51.
    • (2004) Jama , vol.292 , pp. 943-951
    • Neumann, H.P.1    Pawlu, C.2    Peczkowska, M.3    Bausch, B.4    McWhinney, S.R.5    Muresan, M.6
  • 20
    • 84875709120 scopus 로고    scopus 로고
    • Mitochondrial complex II and genomic imprinting in inheritance of paraganglioma tumors
    • Baysal BE. Mitochondrial complex II and genomic imprinting in inheritance of paraganglioma tumors. Biochim Biophys Acta 2013;1827:573-7.
    • (2013) Biochim Biophys Acta , vol.1827 , pp. 573-577
    • Baysal, B.E.1
  • 21
    • 85012938896 scopus 로고    scopus 로고
    • PHEO and paraganglioma syndromes: Genetics and management update
    • Lefebvre M, Foulkes WD. PHEO and paraganglioma syndromes: genetics and management update Curr Oncol 2014;21:8-17.
    • (2014) Curr Oncol , vol.21 , pp. 8-17
    • Lefebvre, M.1    Foulkes, W.D.2
  • 22
    • 84856118165 scopus 로고    scopus 로고
    • The genetics of phaeochromocytoma: Using clinical features to guide genetic testing
    • Jafri M, Maher ER. The genetics of phaeochromocytoma: using clinical features to guide genetic testing. Eur J Endocrinol 2012;166:151-8.
    • (2012) Eur J Endocrinol , vol.166 , pp. 151-158
    • Jafri, M.1    Maher, E.R.2
  • 23
    • 84860834761 scopus 로고    scopus 로고
    • An update on the genetics of paraganglioma, PHEO, and associated hereditary syndromes
    • Gimenez-Roqueplo AP, Dahia PL, Robledo M. An update on the genetics of paraganglioma, PHEO, and associated hereditary syndromes. Horm Metab Res 2012;44:328-33.
    • (2012) Horm Metab Res , vol.44 , pp. 328-333
    • Gimenez-Roqueplo, A.P.1    Dahia, P.L.2    Robledo, M.3
  • 25
    • 58549111025 scopus 로고    scopus 로고
    • Assessment of p27 (cyclin-dependent kinase inhibitor 1B) and aryl hydrocarbon receptor-interacting protein (AIP) genes in multiple endocrine neoplasia (MEN1) syndrome patients without any detectable MEN1 gene mutations
    • Igreja S, Chahal HS, Akker SA, Gueorguiev M, Popovic V, Damjanovic S, Burman P et al. Assessment of p27 (cyclin-dependent kinase inhibitor 1B) and aryl hydrocarbon receptor-interacting protein (AIP) genes in multiple endocrine neoplasia (MEN1) syndrome patients without any detectable MEN1 gene mutations. Clin Endocrinol 2009;70:259-64.
    • (2009) Clin Endocrinol , vol.70 , pp. 259-264
    • Igreja, S.1    Chahal, H.S.2    Akker, S.A.3    Gueorguiev, M.4    Popovic, V.5    Damjanovic, S.6    Burman, P.7
  • 28
    • 66849087634 scopus 로고    scopus 로고
    • Multiple endocrine neoplasias: Advances and challenges for the future
    • Alevizaki M, Stratakis CA Multiple endocrine neoplasias: advances and challenges for the future. J Intern Med 2009;266:1-4.
    • (2009) J Intern Med , vol.266 , pp. 1-4
    • Alevizaki, M.1    Stratakis, C.A.2
  • 29
    • 77955214443 scopus 로고    scopus 로고
    • The North American Neuroendocrine Tumor Society consensus guideline for the diagnosis and management of neuroendocrine tumors: PHEO, paraganglioma, and medullary thyroid cancer
    • Chen H, Sippel RS, O'Dorisio MS, Vinik AI, Lloyd RV, Pacak K. North American Neuroendocrine Tumor Society (NANETS). The North American Neuroendocrine Tumor Society consensus guideline for the diagnosis and management of neuroendocrine tumors: PHEO, paraganglioma, and medullary thyroid cancer. Pancreas. 2010;39:775-83.
    • (2010) Pancreas , vol.39 , pp. 775-783
    • Chen, H.1    Sippel, R.S.2    O'dorisio, M.S.3    Vinik, A.I.4    Lloyd, R.V.5    Pacak, K.6
  • 30
    • 0023789889 scopus 로고
    • Malignant pheocromocytoma: Effective treatment with a combination of cyclophosphamide, vincristine, and dacarbazine
    • Averbuch SD, Steakley CS, Young RC, Gelmann EP, Goldstein DS, Stull R et al. Malignant pheocromocytoma: effective treatment with a combination of cyclophosphamide, vincristine, and dacarbazine. Ann Intern Med 1988;109:267-73.
    • (1988) Ann Intern Med , vol.109 , pp. 267-273
    • Averbuch, S.D.1    Steakley, C.S.2    Young, R.C.3    Gelmann, E.P.4    Goldstein, D.S.5    Stull, R.6
  • 31
    • 84875401017 scopus 로고    scopus 로고
    • Laparoscopic adrenalectomy, a safe procedure for pheochromocytoma. A retrospective review of clinical series
    • Conzo G, Musella M, Corcione F, De Palma M, Ferraro F, Palazzo A, Napolitano S et al. Laparoscopic adrenalectomy, a safe procedure for pheochromocytoma. A retrospective review of clinical series. Int J Surg. 2013;11:152-6.
    • (2013) Int J Surg. , vol.11 , pp. 152-156
    • Conzo, G.1    Musella, M.2    Corcione, F.3    De Palma, M.4    Ferraro, F.5    Palazzo, A.6    Napolitano, S.7
  • 32
    • 84886308081 scopus 로고    scopus 로고
    • Laparoscopic treatment of pheochromocytomas smaller or larger than 6 cm. A clinical retrospective study on 44 patients. Laparoscopic adrenalectomy for pheochromocytoma
    • ConzoG, Musella M, Corcione F, De Palma M, Avenia N, Milone M et al. Laparoscopic treatment of pheochromocytomas smaller or larger than 6 cm. A clinical retrospective study on 44 patients. Laparoscopic adrenalectomy for pheochromocytoma. Ann Ital Chir. 2013;84:417-22.
    • (2013) Ann Ital Chir. , vol.84 , pp. 417-422
    • Conzo, G.1    Musella, M.2    Corcione, F.3    De Palma, M.4    Avenia, N.5    Milone, M.6
  • 33
    • 70350354684 scopus 로고    scopus 로고
    • Novel and evolving therapies in the treatment of malignant phaeochromocytoma: Experience with the mTOR inhibitor everolimus (RAD001)
    • Druce MR1, Kaltsas GA, Fraenkel M, Gross DJ, Grossman AB. Novel and evolving therapies in the treatment of malignant phaeochromocytoma: experience with the mTOR inhibitor everolimus (RAD001). Horm Metab Res 2009;41:697-702.
    • (2009) Horm Metab Res , vol.41 , pp. 697-702
    • Druce, M.R.1    Kaltsas, G.A.2    Fraenkel, M.3    Gross, D.J.4    Grossman, A.B.5
  • 34
    • 59749100013 scopus 로고    scopus 로고
    • Use of the tyrosine kinase inhibitor sunitinib in a patient with von Hippel-Lindau disease: Targeting angiogenic factors in pheocromocytoma and other von Hippel-Lindau disease-related tumors
    • Jimenez C, Cabanillas ME, Santarpia L, Jonasch E, Kyle KL, Lano EA et al. Use of the tyrosine kinase inhibitor sunitinib in a patient with von Hippel-Lindau disease: targeting angiogenic factors in pheocromocytoma and other von Hippel-Lindau disease-related tumors. J Clin Endocrinol Metab. 2009;94:386-91.
    • (2009) J Clin Endocrinol Metab , vol.94 , pp. 386-391
    • Jimenez, C.1    Cabanillas, M.E.2    Santarpia, L.3    Jonasch, E.4    Kyle, K.L.5    Lano, E.A.6
  • 36
    • 70249133742 scopus 로고    scopus 로고
    • Phase II study of high-dose [131I] metaiodobenzylguanidine therapy for patients with metastatic PHEO and paraganglioma
    • Gonias S, Goldsby R, Matthay KK, Hawkins R, Price D, Huberty J et al. Phase II study of high-dose [131I] metaiodobenzylguanidine therapy for patients with metastatic PHEO and paraganglioma. J Clin Oncol 2009;27:4162-8.
    • (2009) J Clin Oncol , vol.27 , pp. 4162-4168
    • Gonias, S.1    Goldsby, R.2    Matthay, K.K.3    Hawkins, R.4    Price, D.5    Huberty, J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.