Preview

Эндокринная хирургия

Расширенный поиск

Феохромоцитома: клинические рекомендации I международного Симпозиума (ISP)

https://doi.org/10.14341/2306-3513-2007-1-3-11

Полный текст:

Аннотация

В рамках I Международного симпозиума по феохромоцитоме (ISP), проведенного в октябре 2005, была обсуждена концепция в отношении катехоламин-продуцирующих опухолей. Были выработаны рекомендации по биохимической и топической диагностике, генетическому обследованию и лечению. В качестве главного диагностического теста и самого точного метода скрининга было рекомендовано определение плазменных или мочевых фракций метанефринов; доверительные интервалы значений метанефринов продемонстрировали наибольшую чувствительность и специфичность. Выбор методов топической диагностики должен основываться на принципе клинической целесообразности. Предоперационная фармакологическая блокада при феохромоцитоме признана обязательной. Генетическое тестирование больных является необходимым в связи с тем, что приблизительно четверть наблюдений феохромоцитом являются результатом герминальных мутаций в пяти вероятных генах; тем не менее этот метод должен применяться по клиническим показаниям, т.к. в настоящее время проверка каждого гена у каждого пациента экономически неэффективна. Показания к конкретному варианту генетического исследования формируются на основании оценки опухолевой локализации, множественности опухолевого поражения, наличию метастазов и типу преобладающей гормональной секреции. Важными проблемами, требующими дальнейшего решения, являются отсутствие адекватных методов дифференциального диагноза злокачественных и доброкачественных опухолей и неудовлетворительные результаты лечения злокачественных опухолей.

Об авторе

D Bel'tsevich



Список литературы

1. Bravo EL et al. (1979) Circulating and urinarycatecholamines in pheochromocytoma. Diagnostic and pathophysiologic implications. N Engl J Med 301: 682-686.

2. Rosano TG et al. (1991) Advances in catecholamine and metabolite measurements for diagnosis of pheochromocytoma. Clin Chem 37: 1854-1867.

3. Young WF Jr (1997) Pheochromocytoma: issues in diagnosis & treatment. Compr Ther 23: 319-326.

4. Eisenhofer G et al. (2003) Pheochromocytoma: rediscovery as a catecholamine-metabolizing tumor. Endocr Pathol 14: 193-212.

5. Gardet V et al. (2001) Lessons from an unpleasant surprise: a biochemical strategy for the diagnosis of pheochromocytoma. J Hypertens 19: 1029-1035.

6. Gerlo E and Sevens C (1994) Urinary and plasma catecholamines and urinary catecholamine metabolites in pheochromocy-toma: diagnostic value in 19 cases. Clin Chem 40: 250-256.

7. Guller U et al. (2006) Detecting pheochromocytoma: defining the most sensitive test. Ann Surg 243: 102-107.

8. Lenders JW et al. (2002) Biochemical diagnosis of pheochromocytoma: which test is best? JAMA 287: 1427-1434.

9. Raber W et al. (2000) Diagnostic efficacy of unconjugated plasma metanephrines for the detection of pheochromocytoma. Arch Intern Med 160: 2957-2963.

10. Sawka AM et al. (2003) 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 88: 553558.

11. Unger N et al. (2006) Diagnostic value of various biochemical parameters for the diagnosis of pheochromocytoma in patients with adrenal mass. Eur J Endocrinol 154: 409-417.

12. Eisenhofer G et al. (2003) Biochemical diagnosis of pheochromocytoma: how to distinguish truefrom false-positive test results. J Clin Endocrinol Metab 88: 2656-2666.

13. Furuta N et al. (1999) Diagnosis of pheochromocytoma using [123I]compared with [131I]-metaiodobenzylguanidine scintigraphy. Int J Urol 6: 119-124.

14. van der Harst E et al. (2001) [(123)I]metaiodobenzylguanidine and [(111)In]octreotide uptake in benign and malignant pheochromo-cytomas. J Clin Endocrinol Metab 86: 685-693.

15. O'Riordain DS et al. (1996) Clinical spectrum and outcome of functional extraadrenal paraganglioma. World J Surg 20: 916-921.

16. Hoegerle S et al. (2002) Pheochromocytomas: detection with 18F DOPA whole body PET-initial results. Radiology 222: 507-512.

17. Ilias I et al. (2002) 6-[18F]-fluorodopamine positron emission tomography versus [131I] metaiodobenzylguanidine scintigraphy in the evaluation of patients with pheochromocytoma. Abstract P3-511. Presented at the 84th Annual Meeting of the Endocrine Society: 2002 June 19-22; San Fransisco, CA.

18. Mann GN et al. (2006) [(11)C]metahydroxyephedrine and [(18)f]fluorodeoxyglucose positron emission tomography improve clinical decision making in suspected pheochromocytoma. Ann Surg Oncol 13: 187-197.

19. Pacak K et al. (2001) 6-[18F]fluorodopamine positron emission tomographic (PET) scanning for diagnostic localization of pheochromocytoma. Hypertension 38: 6-8.

20. Shulkin B et al. (1992) PET scanning with hydroxyephedrine: A new approach to the localization of pheochromocytoma. J Nucl Med 33: 1125-1131.

21. Trampal C et al. (2004) Pheochromocytomas: detection with 11C hydroxyephedrine PET. Radiology 230: 423-428.

22. Shulkin BL et al. (1999) Pheochromocytomas: Imaging with 2-[Fluorine-18]fluoro-2-deoxy-D-glucose PET. Nucl Med 212: 35-41.

23. Ilias I and Pacak K (2004) Current approaches and recommended algorithm for the diagnostic localization of pheochromocy-toma. J Clin Endocrinol Metab 89: 479-491.

24. Mamede M et al. (2006) Discordant localization of 2-[18F]-flu-oro-2-deoxy-D-glucose in 6-[18F]fluorodopamineand [123I]-metaiodobenzylguanidinenegative metastatic pheochromocytoma sites. Nucl Med Commun 27: 31-36.

25. Astuti D et al. (2001) Germline SDHD mutation in familial phaeochromocytoma. Lancet 357: 1181-1182.

26. Astuti D et al. (2001) Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromo-cytoma and to familial paraganglioma. Am J Hum Genet 69: 49-54.

27. Baysal BE et al. (2000) Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Science 287: 848-851.

28. Baysal BE et al. (2002) Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas. J Med Genet 39: 178-183.

29. Gimenez-Roqueplo AP et al. (2003) Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochro-mocytomas. Cancer Res 63: 5615-5621.

30. Maher ER et al. (1991) Von Hippel-Lindau disease: a genetic study. J Med Genet 28: 443-447.

31. Neumann HPH et al. (2002) Germ-line mutations in nonsyn-dromic pheochromocytoma. New Engl J Med 346: 1459-1466.

32. Bryant J et al. (2003) Pheochromocytoma: the expanding genetic differential diagnosis. J Natl Cancer Inst 95: 1196-1204.

33. Gagel RF et al. (1988) The clinical outcome of prospective screening for multiple endocrine neoplasia type 2a. An 18-year experience. N Engl J Med 318: 478-484.

34. Mulligan LM et al. (1993) Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature 363: 458-460.

35. Zeiger MA et al. (1995) Loss of heterozygosity on the short arm of chromosome 3 in sporadic, von Hippel-Lindau disease-associated, and familial pheochromocytoma. Genes Chromosomes Cancer 13: 151-156.

36. Jimenez C et al. (2006) Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes? J Clin Endocrinol Metab 91: 2851-2858.

37. Elder EE et al. (2005) Pheochromocytoma and functional paraganglioma syndrome: no longer the 10% tumor. J Surg Oncol 89: 193-201.

38. Lenders JW et al. (2005) Phaeochromocytoma. Lancet 366: 665-675.

39. Neumann HP et al. (2002) Germ-line mutations in nonsyn-dromic pheochromocytoma. N Engl J Med 346: 1459-1466.

40. Amar L et al. (2005) Genetic testing in pheochromocytoma or functional paraganglioma. J Clin Oncol 23: 8812-8818.

41. Benn DE et al. (2005) Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. J Clin Endocrinol Metab 91: 790-792.

42. Barontini M et al. (2006) Characteristics of pheochromocy-toma in a 4to 20-year-old population. Ann NY Acad Sci 1073: 30-37.

43. Weinhausel A et al. (2003) Long-term follow up of a "sporadic" unilateral pheochromocytoma revealing multiple endocrine neoplasia MEN2A-2 in an elderly woman. Endocr Pathol 14: 375-382.

44. Astuti D et al. (2003) Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility. Clin Endocrinol (Oxf) 59: 728-733.

45. Eisenhofer G et al. (1999) Plasma normetanephrine and metanephrine for detecting pheochromocytoma in von Hippel-Lindau disease and multiple endocrine neoplasia type 2. N Engl J Med 340: 1872-1879.

46. Bravo EL and Tagle R (2003) Pheochromocytoma: stateof-the-art and future prospects. Endocr Rev 24: 539-553.

47. Kinney MA et al. (2002) Perioperative management of pheochromocytoma. J Cardiothorac Vasc Anesth 16: 359-369.

48. Pacak K et al. (2001) Recent advances in genetics, diagnosis, localization, and treatment of pheochromocytoma. Ann Intern Med 134: 315-329.

49. Prys-Roberts C (2000) Phaeochromocytoma-recent progress in its management. Br J Anaesth 85: 44-57.

50. Proye C et al. (1989) Exclusive use of calcium channel blockers in preoperative and intraoperative control of pheochromocytomas: hemodynamics and free catecholamine assays in ten consecutive patients. Surgery 106: 1149-1154.

51. Plouin PF et al. (1997) Tumor recurrence and hypertension persistence after successful pheochromocytoma operation. Hypertension 29: 1133-1139.

52. Janetschek G et al. (1998) Laparoscopic surgery for pheochro-mocytoma: adrenalectomy, partial resection, excision of paragangliomas. J Urol 160: 330-334.

53. Brunt LM et al. (2002) Adrenalectomy for familial pheochro-mocytoma in the laparoscopic era. Ann Surg 235: 713-720.

54. Lee J et al. (1996) Cortical-sparing adrenalectomy for patients with bilateral pheochromocytoma. Surgery 120: 1064-1070.

55. Nambirajan T et al. (2005) Laparoscopic adrenal surgery for recurrent tumours in patients with hereditary phaeochromocytoma. Eur Urol 47: 622-626.

56. Yip L et al. (2004) Surgical management of hereditary pheochromocytoma. J Am Coll Surg 198: 525-534.

57. Koch CA et al. (2002) Pheochromocytoma in von Hippel-Lindau disease: Distinct histopathologic phenotype compared to pheochromocytoma in multiple endocrine neoplasia type 2. Endocr Pathol 13: 17-27.

58. DeLellis RA et al. (Eds; 2004) Tumours of Endocrine Organs. Lyon: IARC Press.

59. Kimura N et al. (2005) Histological grading of adrenal and extra-adrenal pheochromocytomas and relationship to prognosis: a clinicopathological analysis of 116 adrenal pheochromocytomas and 30 extra-adrenal sympathetic paragangliomas including 38 malignant tumors. Endocr Pathol 16: 23-32.

60. Linnoila RI et al. (1990) Histopathology of benign versus malignant sympathoadrenal paragangliomas: clinicopathologic study of 120 cases including unusual histologic features. Hum Pathol 21: 11681180.

61. Thompson LD (2002) Pheochromocytoma of the Adrenal gland Scaled Score (PASS) to separate benign from malignant neoplasms: a clinicopathologic and immunophenotypic study of 100 cases. Am J Surg Pathol 26: 551-566.

62. Lack EE et al. (2003) Recommendations for the reporting of extra-adrenal paragangliomas. The Association of Directors of Anatomic and Surgical Pathology. Hum Pathol 34: 112-113.

63. Association of Directors of Anatomic and Surgical Pathology [http://www.adasp.org] (accessed 15 September 2006).

64. Lack EE (1999) Recommendations for the reporting of tumors of the adrenal cortex and medulla. Association of Directors of Anatomic and Surgical Pathology. Virchows Arch 435: 87-91.

65. The Royal College of Pathologists [http://www.rcpath.org] (accessed 15 September 2006)

66. Eisenhofer G et al. (2004) Malignant pheochromocytoma: current status and initiatives for future progress. Endocr Relat Cancer 11: 423-436.

67. August C et al. (2004) CGH and CD 44/MIB-1 immunohisto-chemistry are helpful to distinguish metastasized from nonmetastasized sporadic pheochromocytomas. Mod Pathol 17: 1119-1128.

68. Goldstein RE et al. (1999) Clinical experience over 48 years with pheochromocytoma. Ann Surg 229: 755-764.

69. John H et al. (1999) Pheochromocytomas: can malignant potential be predicted? Urology 53: 679-683.

70. Proye CA et al. (1994) -The» pheochromocytoma: a benign, intra-adrenal, hypertensive, sporadic unilateral tumor. Does it exist? World J Surg 18: 467-472.

71. Whalen RK et al. (1992) Extra-adrenal pheochromocytoma. J Urol 147: 1-10.

72. Mundschenk J and Lehnert H (1998) Malignant pheochromocytoma. Exp Clin Endocrinol Diabetes 106: 373-376.

73. Brouwers FM et al. (2005) Low molecular weight proteomic information distinguishes metastatic from benign pheochromocytoma. Endocr Relat Cancer 12: 263-272.

74. Averbuch SD et al. (1988) Malignant pheochromocy-toma: effective treatment with a combination of cyclophosphamide, vincristine, and dacarbazine. Ann Intern Med 109: 267-273.

75. Rose B et al. (2003) High-dose 131I-metaiodobenzylguanidine therapy for 12 patients with malignant pheochromocytoma. Cancer 98: 239-248.

76. Safford SD et al. (2003) Iodine-131 metaiodobenzylguanidine is an effective treatment for malignant pheochromocytoma and paraganglioma. Surgery 134: 956-962.

77. Takahashi K et al. (1999) Malignant pheochromocytoma with multiple hepatic metastases treated by chemotherapy and transcatheter arterial embolization. Intern Med 38: 349-354.

78. Loh KC et al. (1997) The treatment of malignant pheochromocytoma with iodine-131 metaiodobenzylguanidine (131I-MIBG): a comprehensive review of 116 reported patients. J Endocrinol Invest 20: 648-658.

79. Mukherjee JJ et al. (2001) Treatment of metastatic carcinoid tumours, phaeochromocytoma, paraganglioma and medullary carcinoma of the thyroid with (131)I-meta-iodobenzylguanidine [(131)I-mIBG]. Clin Endocrinol (Oxf) 55: 47-60.

80. Chan EC and Ho PC (2000) High-performance liquid chromatography/atmospheric pressure chemical ionization mass spectro-metric method for the analysis of catecholamines and metanephrines in human urine. Rapid Commun Mass Spectrom 14: 1959-1964.

81. Crockett DK et al. (2002) Rapid analysis of metanephrine and normetanephrine in urine by gas chromatography-mass spectrometry. Clin Chem 48: 332-337.

82. Lagerstedt SA et al. (2004) Measurement of plasma free metanephrine and normetanephrine by liquid chromatography-tandem mass spectrometry for diagnosis of pheochromocytoma. Clin Chem 50: 603-611.

83. Taylor RL and Singh RJ (2002) Validation of liquid chro-matography-tandem mass spectrometry method for analysis of urinary conjugated metanephrine and normetanephrine for screening of pheochromocytoma. Clin Chem 48: 533-539.


Рецензия

Для цитирования:


. Феохромоцитома: клинические рекомендации I международного Симпозиума (ISP). Эндокринная хирургия. 2007;1(1):3-11. https://doi.org/10.14341/2306-3513-2007-1-3-11

For citation:


Bel'tsevich D.G. Feokhromotsitoma: klinicheskie rekomendatsii I mezhdunarodnogo Simpoziuma (ISP). Endocrine Surgery. 2007;1(1):3-11. (In Russ.) https://doi.org/10.14341/2306-3513-2007-1-3-11

Просмотров: 320


ISSN 2306-3513 (Print)
ISSN 2310-3965 (Online)