Page 6 - Suivi à long terme après résection d’un phéochromocytome
P. 6
Kumar et al.
Références 14. Lenders JW, Pacak K, Walther MM et al. Biochemical diagnosis of pheochromocytoma: Which test is best?
JAMA 2002;287:1427-34. https://doi.org/10.1001/jama.287.11.1427
15. Perry CG, Sawka AM, Singh R et al. The diagnostic efficacy of urinary fractionated metanephrines measured
1. Bravo EL, Tagle R. Pheochromocytoma: State-of-the-art and future prospects. Endocr Rev 2003;24:539-53. by tandem mass spectrometry in detection of pheochromocytoma. Clin Endocrinol (Oxf) 2007;66:703-8/
https://doi.org/10.1210/er.2002-0013 https://doi.org/10.1111/j.1365-2265.2007.02805.x
2. Nakamura E, Kaelin WG Jr. Recent insights into the molecular pathogenesis of pheochromocytoma and 16. Amar L, Lussey-Lepoutre C, Lenders JW et al. Recurrence or new tumors after complete resection of
paraganglioma. Endocr Pathol 2006;17:97-106. https://doi.org/10.1385/EP:17:2:97 pheochromocytomas and paragangliomas: A systematic review and meta-analysis. Eur J Endocrinol
3. Benn DE, Robinson BG. Genetic basis of pheochromocytoma and paraganglioma. Best Pract Res Clin 2016;175:R135-45. https://doi.org/10.1530/EJE-16-0189
Endocrinol Metab 2006;20:435-50. https://doi.org/10.1016/j.beem.2006.07.005 17. Plouin PF, Amar L, Dekkers OM et al. European Society of Endocrinology clinical practice guideline for
4. Ilias I, Pacak K. Current approaches and recommended algorithm for the diagnostic localization of pheo- long-term followup of patients operated on for a pheochromocytoma or a paraganglioma. Eur J Endocrinol
chromocytoma. J Clin Endocrinol Metab 2004;89:479-91. https://doi.org/10.1210/jc.2003-031091 2016;174:G1-0. https://doi.org/10.1530/EJE-16-0033
5. Lenders JW, Eisenhofer G, Mannelli M et al. Pheochromocytoma. Lancet 2005;366:665-75. 18. Eisenhofer G, Goldstein DS, Walther MM et al. Biochemical diagnosis of pheochromocytoma: How
https://doi.org/10.1016/S0140-6736(05)67139-5 to distinguish true- from false-positive test results. J Clin Endocrinol Metab 2003b;88:2656-66.
6. Scholz T, Eisenhofer G, Pacak K et al. Current treatment of malignant pheochromocytoma. J Clin Endocrinol https://doi.org/10.1210/jc.2002-030005
Metab 2007;92:1217-25. https://doi.org/10.1210/jc.2006-1544 19. Algeciras-Schimnich A, Preissner CM, Young WF Jr et al. Plasma chromogranin A or urine fractionated
7. Lenders JW, Duh QY, Eisenhofer G et al. Pheochromocytoma and paraganglioma: An endocrine society metanephrines followup testing improves the diagnostic accuracy of plasma fractionated metanephrines for
clinical practice guideline. J Clin Endocrinol Metab 2014;99:1915-42. https://doi.org/10.1210/ pheochromocytoma. J Clin Endocrinol Metab 2008;93:91-5. https://doi.org/10.1210/jc.2007-1354
jc.2014-1498 20. Timmers HJ, Pacak K, Huynh TT et al. Biochemically silent abdominal paragangliomas in patients with
8. Amar L, Servais A, Gimenez-Roqueplo AP et al. Year of diagnosis, features at presentation, and risk mutations in the succinate dehydrogenase subunit B gene. J Clin Endocrinol Metab 2008;93:4826-32.
of recurrence in patients with pheochromocytoma or secreting paraganglioma. J Clin Endocrinol Metab https://doi.org/10.1210/jc.2008-1093
2005b;90:2110-6. https://doi.org/10.1210/jc.2004-1398 21. Gimenez-Roqueplo AP, Caumont-Prim A, Houzard C et al. Imaging workup for screening of paraganglioma
9. Plouin PF, Gimenez-Roqueplo AP. Initial workup and long-term followup in patients with pheo- and pheochromocytoma in SDHx mutation carriers: A multicenter prospective study from the PGL.EVA
chromocytomas and paragangliomas. Best Pract Res Clin Endocrinol Metab 2006a;20:421-34. Investigators. J Clin Endocrinol Metab 2013;98:E162-73. https://doi.org/10.1210/jc.2012-2975
https://doi.org/10.1016/j.beem.2006.07.004 22. Timmers HJ, Chen CC, Carrasquillo JA et al. Staging and functional characterization of pheochromocytoma
10. Hamidi O, Young WF Jr, Iniguez-Ariza NM et al. Malignant pheochromocytoma and paraganglioma: 272 and paraganglioma by 18F- fluorodeoxyglucose (18F-FDG) positron emission tomography. J Natl Cancer
patients over 55 years. J Clin Endocrinol Metab 2017;102:3296-305. https://doi.org/10.1210/ Inst 2012;104:700-8. https://doi.org/10.1093/jnci/djs188
jc.2017-00992 23. Baudin E, Habra MA, Deschamps F et al. Therapy of endocrine disease: treatment of malignant pheo-
11. Favier J, Amar L, Gimenez-Roqueplo AP. Paraganglioma and pheochromocytoma: From genetics to person- chromocytoma and paraganglioma. Eur J Endocrinol 2014;171:R111-22. https://doi.org/10.1530/
alized medicine. Nat Rev Endocrinol 2015;11:101-11. https://doi.org/10.1038/nrendo.2014.188 EJE-14-0113
12. Eisenhofer G, Peitzsch M. Laboratory evaluation of pheochromocytoma and paraganglioma. Clin Chem
2014;60:1486-99. https://doi.org/10.1373/clinchem.2014.224832 r
13. Lenders JW, Keiser HR, Goldstein DS et al. Plasma metanephrines in the diagnosis of pheochromocytoma. Correspondence: D Neal Rowe, Division d’urologie, Département de chirurgie, L’Hôpital d’Ottawa,
Ann Intern Med 1995;123:101-9. https://doi.org/10.7326/0003-4819-123-2-199507150-00004 Université d’Ottawa, Ottawa (Ont.), Canada; nealrowe81@gmail.com
R102 CUAJ • Décembre 2019 • Volume 13, numéro 12