Diagnosis of and surgical therapy for pheochromocytoma and paraganglioma;Diagnostik und operative Therapie von Phäochromozytomen und Paragangliomen

Zentralblatt fur Chirurgie - Zeitschrift fur Allgemeine, Viszeral- und Gefasschirurgie

Volumn 135, Issue 3, 2010, Pages 226-232

  Musholt, T J ^a  

^a JOHANNES GUTENBERG UNIVERSITY   (Germany)

Author keywords

Abdominal surgery; Endocrine surgery; MEN; Paraganglioma; PGL; Pheochromocytoma

Indexed keywords

ADRENAL GLAND; ADRENAL TUMOR; ADRENALECTOMY; ARTICLE; DIFFERENTIAL DIAGNOSIS; HUMAN; METHODOLOGY; MINIMALLY INVASIVE SURGERY; MULTIPLE ENDOCRINE NEOPLASIA; PARAGANGLIOMA; PATHOLOGY; PHEOCHROMOCYTOMA;

ADRENAL GLAND NEOPLASMS; ADRENAL GLANDS; ADRENALECTOMY; DIAGNOSIS, DIFFERENTIAL; HUMANS; MULTIPLE ENDOCRINE NEOPLASIA; PARAGANGLIOMA; PHEOCHROMOCYTOMA; SURGICAL PROCEDURES, MINIMALLY INVASIVE;

EID: 77953660148     PISSN: 0044409X     EISSN: 14389592     Source Type: Journal    
DOI: 10.1055/s-0030-1247315     Document Type: Article

References (44)

1. Fränkel F. Ein Fall von doppelseitigem vllig latent verlaufendem Nebennierentumor und gleichzeitiger Nephritis mit Veränderungen am Circulationsapparat und Retinitis. Virchows Arch Pathol Physiol 1886 103 224-263
2. McNicol A M., Young W F., Kawashima A et al. Benign pheochromocytoma. In: DeLellisRA, LloydRV, HeitzPU, EngC, eds. World Health Organization Classification of Tumors pathology and genetics: Tumors of Endocrine Organs. Lyon: IARC Press; 2004: 151155
3. Kimura N, Chetty R, Capella C et al. Extra-adrenal paraganglioma: carotid body, jugulotympanic, vagal, laryngeal, aortico-pulmonary. In: DeLellisRA, LloydRV, HeitzPU, EngC, eds. World Health Organization Classification of Tumors pathology and genetics: Tumors of Endocrine Organs. Lyon: IARC Press; 2004: 159161
4. Neumann H P., Eng C. The approach to the patient with paraganglioma. JClin Endocrinol Metab 2009 94 2677-2683
5. Tischler A S., Kimura N, McNicol A M. Pathology of pheochromocytoma and extra-adrenal paraganglioma. Ann N Y Acad Sci 2006 1073 557-570
6. Stenstrom G, Svardsudd K. Pheochromocytoma in Sweden 19581981. An analysis of the National Cancer Registry Data. Acta Med Scand 1986 220 225-232
7. Beard C M., Carney J A., Sheps S G. et al. Incidence of phaeochromocytoma. J Hum Hypertens 1989 3 481-481
8. McNichol A M. Differential diagnosis of pheochromocytomas and paragangliomas. Endocr Pathol 2001 12 407-415
9. Erickson D, Kudva Y C., Ebersold M J. et al. Benign paragangliomas: clinical presentation and treatment outcomes in 236 patients. J Clin Endocrinol Metab 2001 86 5210-5216
10. Kopetschke R, Slisko M, Kilisli A et al. Frequent incidental discovery of phaeochromocytoma: data from a German cohort of 201phaeochromocytoma. Eur J Endocrinol 2009 161 355-361
11. Karagiannis A, Mikhailidis D P., Athyros V G. et al. Pheochromocytoma: an update on genetics and management. Endocr Relat Cancer 2007 14 935-956
12. Kloppel G. Tumoren des Nebennierenmarks und der Paraganglien. Pathologe 2003 24 280-286
13. Neumann H P., Bausch B, McWhinney S R. et al. Germ-line mutations in nonsyndromic pheochromocytoma. N Engl J Med 2002 346 1459-1466
14. Amar L, Bertherat J, Baudin E et al. Genetic testing in pheochromocytoma or functional paraganglioma. J Clin Oncol 2005 23 8812-8818
15. Gimm O. Pheochromocytoma-associated syndromes: genes, proteins and functions of RET, VHL and SDHx. Fam Cancer 2005 4 17-23
16. Waldmann J, Bartsch D K., Kann P H. et al. Adrenal involvement in multiple endocrine neoplasia type1: results of 7years prospective screening. Langenbecks Arch Surg 2007 392 437-443
17. van der Harst E, Bruining H A., Jaap Bonjer H et al. Proliferative index in phaeochromocytomas: does it predict the occurrence of metastases? JPathol 2000 191 175-180
18. Thompson L DR, Young W F., Kawashima A et al. Malignant adrenal phaeochromocytoma. In: DeLellis RA, Lloyd RV, Heitz PU, Eng C, eds. World Health Organization Classification of Tumors pathology and genetics: Tumors of Endocrine Organs. Lyon: IARC Press; 2004: 147150
19. Scholz T, Eisenhofer G, Pacak K et al. Clinical review: Current treatment of malignant pheochromocytoma. J Clin Endocrinol Metab 2007 92 1217-1225
20. Shen W T., Sturgeon C, Clark O H. et al. Should pheochromocytoma size influence surgical approach? A comparison of 90malignant and 60benign pheochromocytomas. Surgery 2004 136 1129-1137
21. Wu D, Tischler A S., Lloyd R V. et al. Observer variation in the application of the Pheochromocytoma of the Adrenal Gland Scaled Score. Am J Surg Pathol 2009 33 599-608
22. Wangberg B, Muth A, Khorram-Manesh A et al. Malignant pheochromocytoma in a population-based study: survival and clinical results. Ann N Y Acad Sci 2006 1073 512-516
23. Eisenhofer G, Goldstein D S., Walther M M. et al. Biochemical diagnosis of pheochromocytoma: how to distinguish true- from false-positive test results. J Clin Endocrinol Metab 2003 88 2656-2666
24. Jimenez C, Cote G, Arnold A et al. Review: Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes? J Clin Endocrinol Metab 2006 91 2851-2858
25. Greenblatt D Y., Shenker Y, Chen H. The utility of metaiodobenzylguanidine (MIBG) scintigraphy in patients with pheochromocytoma. Ann Surg Oncol 2008 15 900-905
26. 123)I-MIBG scintigraphy for patients with phaeochromocytoma is not necessary. Langenbecks Arch Surg 2008 393 725-727
27. 18F-FDG-PET in the management of malignant and multifocal phaeochromocytomas. Clin Endocrinol (Oxf) 2008 69 580-586
28. Apgar V, Papper E M. Pheochromocytoma. Anesthetic management during surgical treatment. AMA Arch Surg 1951 62 634-648
29. Graham J B. Pheochromocytoma and hypertension; an analysis of 207cases. Int Abstr Surg 1951 92 105-121
30. Weismann D, Fassnacht M, Weinberger F et al. Intraoperative haemodynamic stability in patients with phaeochromocytoma minimally invasive vs conventional open surgery. Clin Endocrinol (Oxf) 2006 65 352-358
31. Gray D K., Thompson N W. Pheochromocytoma. In: DohertyGM, SkogseidB, eds. Surgical Endocrinology. Philadelphia: Lippincott Williams&Wilkins; 2001: 247261
32. Prichard B N., Ross E J. Use of propranolol in conjunction with alpha receptor blocking drugs in pheochromocytoma. Am J Cardiol 1966 18 394-398
33. Proye C, Fossati P, Fontaine P et al. Dopamine-secreting pheochromocytoma: an unrecognized entity? Classification of pheochromocytomas according to their type of secretion. Surgery 1986 100 1154-1162
34. Walz M K., Petersenn S, Koch J A. et al. Endoscopic treatment of large primary adrenal tumours. Br J Surg 2005 92 719-723
35. Brauckhoff M, Gimm O, Dralle H. Preoperative and surgical therapy in sporadic and familial pheochromocytoma. Front Horm Res 2004 31 121-144
36. Walz M K., Peitgen K, Neumann H P. et al. Endoscopic treatment of solitary, bilateral, multiple, and recurrent pheochromocytomas and paragangliomas. World J Surg 2002 26 1005-1012
37. Musholt T J. Surgical management of advanced malignant adrenal tumors. Eur Surg 2003 35 97-101
38. Hanazawa K, Koizumi K, Tanaka M et al. Total replacement of the aorta and the inferior vena cava after resection of an extra-adrenal malignant pheochromocytoma. Urol Int 2000 64 108-110
39. Chrisoulidou A, Kaltsas G, Ilias I et al. The diagnosis and management of malignant phaeochromocytoma and paraganglioma. Endocr Relat Cancer 2007 14 569-585
40. Forrer F, Riedweg I, Maecke H R. et al. Radiolabeled DOTATOC in patients with advanced paraganglioma and pheochromocytoma. Q J Nucl Med Mol Imaging 2008 52 334-340
41. Averbuch S D., Steakley C S., Young R C. et al. Malignant pheochromocytoma: effective treatment with a combination of cyclophosphamide, vincristine, and dacarbazine. Ann Intern Med 1988 109 267-273
42. Huang H, Abraham J, Hung E et al. Treatment of malignant pheochromocytoma/paraganglioma with cyclophosphamide, vincristine, and dacarbazine: recommendation from a 22-year follow-up of 18patients. Cancer 2008 113 2020-2028
43. Eisenhofer G, Bornstein S R., Brouwers F M. et al. Malignant pheochromocytoma: current status and initiatives for future progress. Endocr Relat Cancer 2004 11 423-436
44. Pacak K, Linehan W M., Eisenhofer G et al. Recent advances in genetics,diagnosis, localization, and treatment of pheochromocytoma. Ann Intern Med 2001 134 315-329