101
Views
17
CrossRef citations to date
0
Altmetric
Review Papers

Phaeochromocytoma: State-of-the-art

&
Pages 140-148 | Published online: 11 Mar 2016

References

  • Frankel F. Ein fall von doppelseitigem, völlig latent verhaufenen nebennierentumor und gleichzeitiger nephritis mit veränderungen am circulationapparat und retinitis. Arch Pathol Anat Physiol Klin Med, 1886, 103: 244–263.
  • Neumann H. P. H., Vortmeyer A., Schmidt D., Wermer M., Erlic Z., Cascon A., et al. Evidence of MEN-2 in the original description of classic pheochromocytoma. N Engl J Med, 2007, 357: 1311–1315.
  • Bravo E. L., Tagle R. Pheochromocytoma: State-of-the-Art and future prospects. Endocr Rev, 2003, 24: 539–553.
  • Karagiannis A., Mikhailidis D. P., Athyros V. S., Harsoulis F. Pheochromocytoma: an update on genetics and management. Endocrine-Related Cancer, 2007, 14: 935–936.
  • Young W. Endocrine hypertension. In: Williams Texbook of Endocrinology, 505–537. Saunders, Philadelphia, 2008.
  • Adler J. T., Meyer-Rochon G. Y., Chen H., Benn D. E., Robinson B. G., Sippel R. S., Sidhu SB. Pheochromocytoma: current approaches and future directions. The Oncologist, 2008, 13: 779–793.
  • Amar L., Gimenez-Roqueplo A. P., Hernigou A., Plouin J. P. Phéochromocytomes. In: Traité d’Endocrinologie 380–386. Médecine-Sciences. Flammarion, Paris, 2007.
  • Mantero F., Terzolo M., Arnaldi G., Osella G., Masini A. M., Ali A. et al. A survey on adrenal incidentaloma in Italy. Study group on adrenal tumors of the Italian Society of Endocrinology. J Clin Endocrinol Metab, 2000, 85: 637–644.
  • McNeil A. R., Blok B. H., Koelmeyer J. D., Burke M. P., Hilton J. M. Pheochromocytomas discovered during coronial autopsies in Sydney, Melbourne and Auckland. Aust NZ J Med, 2000, 30: 648–652.
  • Bravo E. L., Gilford R. W. Jr. Current concepts. Pheochromocytoma: diagnosis, localization and management. NEngl J Med, 1984, 311: 1298–1303.
  • Neumann H. P., Bausch B., Mc Whinney S. R., Bender B. U., Gimm O., Franke G. et al. Germ-line mutations in nonsyndromic pheochromocytoma. N Engl J Med, 2002, 346: 1459–1466.
  • Amar L., Bertherat J., Baudin E., Ajzenberg C., Bressac-de Paillerets B., Chabre O. et al. Genetic testing in pheochromocytoma or functional paraganglioma. J Clin Oncol, 2005, 23: 88128818.
  • Gimenez-Roqueplo A. P., Lehnery H., Mannelli M., Neumann H., Opocher G., Mahner E. R., Plouin J. P., on behalf of the European Network for the Study of Adrenal Tumours (ENS@T). Pheochromocytoma Working Group. Pheochromocytoma, new genes and screening strategies. Clin Endocrinol, 2006, 65: 699–705.
  • Jimenez C., Cote G., Arnold A., Gagel RF. Should patients with apparent by sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes ? J Clin Endocrinol Metab, 2006, 91: 2851–2858.
  • Baysal B. E., Ferrell R. E., Willett-Brozick J. E., Lawrence E. C., Myssiorek D., Bosch A. et al. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Science, 2000, 287: 848–851.
  • Donckier J. E. Endocrine diseases and diabetes. In: Textbook of Diabetes. 27.1–27.25. Blackwell Science, Oxford, 2003.
  • Donckier J. E., Rosière A., Heureux F., Michel L. Diabetes Mellitus as a primary manifestation of multiple endocrine neoplasia type 2 B. Acta Chir Belg, 2008, 108: 732–737.
  • Col V., de Cannière L., Messaoudi L., Michel L., Donckier J. Heart failure induced by pheochromocytoma: laparoscopic treatment and intraoperative changes of several new cardiovascular hormones. Horm Res, 1999, 51: 50–52.
  • Donckier J. E., Delgrange E., Michel L. ECG abnormalities of endocrine origin. Heart, 2001, 85: 679.
  • Sakel S. G., Manson J. E., Marawi S. T., Burokoff R. Watery diarrhoea syndrome due to an adrenal pheochromocytoma secreting vasoactive intestinal peptide. Dig Dis Sci, 1985, 30: 1201–1207.
  • Mune T., Katakami H., Kato Y., Yasuda K., Matsukura S., Miura K. Production and secretion of parathyroid hormone-related protein in pheochromocytoma: participation of an a-adrenergic mechanism. J Clin Endocrinol Metab, 1993, 76: 757–762.
  • Hes F. J., Hoppener J. W. M., Lipas C. J. M. Pheochromocytoma in von Hippel-Lindau disease. J Clin Endocrinol Metab, 2003, 88: 969–974.
  • Lenders J. W. M., Pacak K., Walther M. M., Lineham W. M., Mannelli M., Friber G. P. et al. Biochemical diagnosis of pheochromocytoma: which test is best ? JAMA, 2002, 287: 14271434.
  • Sawka A. M., Jaeschker R., Singh R. J., Young W. F. Jr. A comparison of biochemical tests for pheochromocytoma: measurement of fractionated plasma metanephrines compared with the combination of 24-hour urinary metanephrines and catecholamines. J Clin Endocrinol Metab, 2003, 88: 553–558.
  • Canale M. P., Bravo E. L. Diagnostic specificity of serum chromogranin-A for pheochromocytoma in patients with renal dysfunction. J Clin Endocrinol Metab, 1994, 78: 1139–1144.
  • Grossrubatscher E., Dalino P., Vignati F., Gambacorta M., Pugliese R., Boniardi M. et al. The role of chromogranin-A in the management of patients with pheochromocytoma. Clin Endocrinol, 2006, 65: 287–293.
  • Rao F., Keiser H. R., O’Connor D. T. Malignant and benign pheochromocytoma: chromaffin granule transmitters and the response to medical and surgical treatment. Ann NY Acad Sci, 2002, 97: 530–532.
  • van der Harst E., de Herder W. W., de Krugger R. R., Bruining H. A., Bonjer H. J., Lamberts S. W. et al. The value of plasma markers for the clinical behaviour of pheochromocytomas. Eur J Endocrinol, 2002, 147: 85–94.
  • Donckier J., Michel L., Collard E., Berbinschi A., Ketelslegers J. M., Harvengt C. Parallel changes of atrial natriuretic factor and catecholamines during surgery for pheochro-mocytoma. Am J Med, 1988, 85: 278–279.
  • Mouri T., Sone M., Takahashi K., Itoi K., Totsune K., Hayashi Y. Neuropeptide Y as a plasma marker for pheochromocytoma, gan-glioneuroblastoma and neuroblastoma. Clin Sci, 1992, 83: 205–211.
  • Eisenhofer G., Goldstein D. S., Walther M. M., Friberg P., Lenders J. W. M., Keiser H. R. et al. Biochemical diagnosis of pheochromocytoma: how to distinguish true-from false-positive test results. J Clin Endocrinol Metab, 2003, 88: 2656–2666.
  • van der Harst E., de Herder W. W., Bruining H. A., Bonjer H. J., de Krijger R. R., Lamberts S. W. et al. [123I] Metaiodobenzyl-guanidine and [111 In] octreotide uptake in benign and malignant pheochromocytoma. J Clin Endocrinol Metab, 2001, 86: 685–693.
  • Newbould E. C., Ross G. A., Dacie J. E., Bouloux P. M., Besser G. M., Grossman A. The use of venous catheterization in the diagnosis and localisation of bilateral pheochromocytomas. Clin Endocrinol, 1991, 35: 55–59.
  • Prys-Roberts C. Phaeochromocytoma-recent progress in its management. Br J Anaesth, 2000, 85: 44–57.
  • James M. F. M. Use of magnesium sulphate in the anaesthetic management of phaeochromocytoma: a review of 17 anaesthetics. Br J Anaesth, 1989, 62: 616–623.
  • James M. F., Cronje L. Pheochromocytoma crisis: the use of magnesium sulphate. Anesth Analg, 2004, 99: 680–686.
  • Gagner M., Lacroix A., Bolté E. Laparoscopic adrenalectomy in Cushing’s syndrome and pheochromocytoma. N Engl J Med, 1992, 327: 1033.
  • Col V., de Cannière L., Collard E., Michel L., Donckier J. Laparoscopic adrenalectomy for phaeochromocytoma: endocrino-logical and surgical aspects of a new therapeutic approach. Clin Endocrinol, 1999, 50: 121–125.
  • Michel L. A., Donckier J. E. Importance of secretion pattern in minimally invasive surgery for phaeochromocytoma. Clin Endocrinol, 2006, 66: 455–456.
  • Michel L. A., de Cannière L., Hamoir E., Hubens G., Meurisse M., Squifflet J. P. Asymptomatic adrenal tumours: criteria for endoscopic removal. Eur J Surg, 1999, 165: 767–771.
  • Salmenkivi K., Arola J., Voutailainen R., Ilvesmaki V., Haglund C., Kahri A. I. et al. Inhibin/activin betaB-subunit expression in phaeochromocytoma favors benign diagnosis. J Clin Endocrinol Metab, 2001, 86: 2231–2235.
  • Helman L. J., Cohen P. S., Averbuch S. D., Cooper M. J., Keiser H. R., Israel M. A. Neuropeptide Y expression distinguishes malignant from benign phaeochromocytoma. J Clin Oncol, 1989, 7: 1720–1725.
  • Loh K. C., Fitzgerald P. A., Mattay K. K., Yeo P. P., Price D. C. The treatment of malignant phaeochromocytoma with iodine-131 metaiodobenzylguanidine (131I-MIBG): a comprehensive review of 116 reported patients. J Endocrinol Invest, 1997, 20: 648–658.
  • Kaltsas G. A., Papadogias D., Makras P., Grossman A. B. Treatment of advanced neuroendocrine tumours with radiolabelled somatostatin analogues. Endocr Relat Cancer, 2005, 12: 683–699.
  • Averbuch S. D., Steakley C. S., Young R. C., Gelmann E. P., Goldstein D. S., Stull R., Keiser H. R. Malignant phaeochromo-cytoma: effective treatment with a combination of cyclophos-phamide, vincristine and dacarbazine. Ann Intern Med, 1988, 109: 267–277.
  • Sisson J. C., Shapiro B., Shulkin B. L. et al. Treatment of malignant pheochromocytomas with 131–1 metabenzylguanidine and chemotherapy. Am J Clin Oncol, 1999, 22: 364–370.
  • Sausville E. A., Tomaszewski J. E., Ivy P. Clinical development of 17-allylamino,17-demethoxygeldanamycin. Curr Cancer Drug Targets, 2003, 3: 377–383.
  • Manelli M. Management and treatment of phaeochromocytomas and paragangliomas. Ann NY Acad Sci, 2006, 1073: 405–416.
  • Manelli M., Bemporad D. Diagnosis and management of phaeochromocytoma during pregnancy. J Endocrinol Invest, 2002, 25: 567–571.
  • Wattanachanya L., Bunworasate U., Plengpanich W., Houngngam N., Buranasupkajom P., Sunthormyothin S. et al. Bilateral pheochromocytoma during the postpartum period. Arch Gynecol Obstet, 2009, 280 :1055–1058.
  • Kim J., Reutrakul S., Davis D. B., Kaplan E. L., Refetoff S. Multiple endocrine neoplasia 2A presenting as peripartum cardio-myopathy due to catecholamine excess. Eur J Endocrinol, 2004, 151: 771–777.
  • Frayssinet C., Vezzosi D., Huyghe E., Lorenzini F., Bennet A., Caron P. Retroperitoneal laparoscopic adrenalectomy in a pregnant woman presenting MEN 2A with a phaeochromocytoma: case report and review of the literature. Ann Endocrinol (Paris), 2008, 69: 53–57.
  • Stenstrom G., Swolin K. Pheochromocytoma in pregnancy. Experience of treatment with phenoxybenzamine in three patients. Acta Obstet Gynecol Scand, 1985, 64: 357–361.
  • Brandi M. L., Gagel R. F., Angeli A., Bilezikian J. P., Peck-Peccoz P., Bordi C. et al. Guidelines for diagnosis and therapy of MEN type 1 and type 2. J Clin Endocrinol Metab, 2001, 86: 56585671.
  • Lips C. J. M. Clinical management of the multiple endocrine neoplasia syndromes: results of a computerized opinion poll at the Sixth International Workshop on multiple endocrine neoplasia and von Hippel-Lindau disease. J Intern Med, 1998, 243: 589–594.
  • Huang S. M., Tao B. L., Tzeng C. C., Liu H. T., Wang W. P. Prenatal molecular diagnosis of RET protooncogene mutation in multiple endocrine neoplasia type 2A. J Formos Med Assoc, 1997, 96: 542–544.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.