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  • Review Article
  • Published:

Surgical management of adrenocortical tumours

Key Points

  • A thorough biochemical evaluation is required before a patient with an adrenal tumour can be considered for surgery

  • Careful assessment of imaging characteristics is required to provide an optimum operative approach for patients with suspected adrenocortical carcinoma

  • Transperitoneal and posterior retroperitoneal open or laparoscopic approaches have distinct advantages and disadvantages

  • The treatment of patients with adrenal cancer should be managed by clinicians with experience in treating this rare disease

Abstract

The surgical treatment of adrenal tumours has evolved over the past century, as has our understanding of which hormones are secreted by the adrenal glands and what these hormones do. This article reviews the preoperative evaluation of patients with adrenal tumours that could be benign or malignant, including metastases. The biochemical evaluation of excess levels of hormones is discussed, as are imaging characteristics that differentiate benign tumours from malignant tumours. The options for surgical management are outlined, including the advantages and disadvantages of various open and laparoscopic approaches. The surgical management of adrenocortical carcinoma is specifically reviewed, including controversies in operative approaches as well as surgical management of invasive or recurrent disease.

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Figure 1: CT images showing a benign adrenal tumour.
Figure 2: CT image of a tumour amenable to an anterior open or a laparoscopic approach.
Figure 3: CT image of a tumour amenable to a posterior laparoscopic approach.
Figure 4: CT image demonstrating adenoma emanating off the posterior limb of the right adrenal gland in a patient with Conn syndrome that is amenable to partial adrenalectomy.
Figure 5: Illustration of a technique for removing a portion of the adrenal gland from a peripheral or central location within the adrenal gland.
Figure 6: Classification schema for intracaval tumour thrombus.

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References

  1. Hergus, S. & Lynn, J. in Surgical Endocrinology (ed. Lynn J. & Bloom S.) 458–467 (Buttersworth/Heinemann, London, 1993).

    Google Scholar 

  2. Greenblatt, R. B. in Search the Scriptures 3rd edn 45–48 (J. P. Lippincott, Philadelphia, 1977).

    Google Scholar 

  3. Gagner, M., Lacroix, A. & Bolte, E. Laparoscopic adrenalectomy in Cushing's syndrome and pheochromocytoma [letter]. N. Engl. J. Med. 327, 1033 (1992).

    Article  CAS  PubMed  Google Scholar 

  4. Gagner, M. et al. Early experience with laparoscopic approach for adrenalectomy. Surgery 114, 1120–1125 (1993).

    CAS  PubMed  Google Scholar 

  5. Zeiger, M. A. et al. The American Association of Clinical Endocrinologists and American Association of Endocrine Surgeons medical guidelines for the management of adrenal incidentalomas. Endocr. Pract. 15 (Suppl. 1), 1–20 (2009).

    Article  PubMed  Google Scholar 

  6. Grumbach, M. M. et al. Management of the clinically inapparent adrenal mass (“incidentaloma”). Ann. Intern. Med. 138, 424–429 (2003).

    Article  PubMed  Google Scholar 

  7. [No authors listed] NIH state-of-the-science statement on management of the clinically inapparent adrenal mass (“incidentaloma”). NIH Consens. State Sci. Statements 19, 1–25 (2002).

  8. Johnson, P. T., Horton, K. M. & Fishman, E. K. Adrenal mass imaging with multidetector CT: pathologic conditions, pearls, and pitfalls. Radiographics 29, 1333–1351 (2009).

    Article  PubMed  Google Scholar 

  9. Bharwani, N. et al. Adrenocortical carcinoma: the range of appearances on CT and MRI. AJR Am. J. Roentgenol. 196, W706–W714 (2011).

    Article  PubMed  Google Scholar 

  10. Dunnick, N. R., Heaston, D., Halvorsen, R., Moore, A. V. & Korobkin, M. CT appearance of adrenal cortical carcinoma. J. Comput. Assist. Tomogr. 6, 978–982 (1982).

    Article  CAS  PubMed  Google Scholar 

  11. Berland, L. L. et al. Managing incidental findings on abdominal CT: white paper of the ACR incidental findings committee. J. Am. Coll. Radiol. 7, 754–773 (2010).

    Article  PubMed  Google Scholar 

  12. Hussain, S. et al. Differentiation of malignant from benign adrenal masses: predictive indices on computed tomography. AJR Am. J. Roentgenol. 144, 61–65 (1985).

    Article  CAS  PubMed  Google Scholar 

  13. Haider, M. A., Ghai, S., Jhaveri, K. & Lockwood, G. Chemical shift MR imaging of hyperattenuating (>10 HU) adrenal masses: does it still have a role? Radiology 231, 711–716 (2004).

    Article  PubMed  Google Scholar 

  14. Caoili, E. M., Korobkin, M., Francis, I. R., Cohan, R. H. & Dunnick, N. R. Delayed enhanced CT of lipid-poor adrenal adenomas. AJR Am. J. Roentgenol. 175, 1411–1415 (2000).

    Article  CAS  PubMed  Google Scholar 

  15. Slattery, J. M. et al. Adrenocortical carcinoma: contrast washout characteristics on CT. AJR Am. J. Roentgenol. 187, W21–W24 (2006).

    Article  PubMed  Google Scholar 

  16. Elsayes, K. M. et al. Adrenal masses: MR imaging features with pathologic correlation. Radiographics 24, (Suppl. 1), S73–S86 (2004).

    Article  PubMed  Google Scholar 

  17. Fishman, E. K. et al. Primary adrenocortical carcinoma: CT evaluation with clinical correlation. AJR Am. J. Roentgenol. 148, 531–535 (1987).

    Article  CAS  PubMed  Google Scholar 

  18. Egbert, N., Elsayes, K. M., Azar, S. & Caoili, E. M. Computed tomography of adrenocortical carcinoma containing macroscopic fat. Cancer Imaging 10, 198–200 (2010).

    Article  PubMed  PubMed Central  Google Scholar 

  19. Remer, E. M. et al. ACR Appropriateness Criteria® Incidentally discovered adrenal mass. American College of Radiology [online], (2012).

    Google Scholar 

  20. Sturgeon, C., Shen, W. T., Clark, O. H., Duh, Q. Y. & Kebebew, E. Risk assessment in 457 adrenal cortical carcinomas: how much does tumor size predict the likelihood of malignancy? J. Am. Coll. Surg. 202, 423–430 (2006).

    Article  PubMed  Google Scholar 

  21. Seccia, T. M., Fassina, A., Nussdorfer, G. G., Pessina, A. C. & Rossi, G. P. Aldosterone-producing adrenocortical carcinoma: an unusual cause of Conn's syndrome with an ominous clinical course. Endocr. Relat. Cancer 12, 149–159 (2005).

    Article  PubMed  Google Scholar 

  22. Kendrick, M. L. et al. Aldosterone-secreting adrenocortical carcinomas are associated with unique operative risks and outcomes. Surgery 132, 1008–1011 (2002).

    Article  PubMed  Google Scholar 

  23. Groussin, L. et al. 18F-Fluorodeoxyglucose positron emission tomography for the diagnosis of adrenocortical tumors: a prospective study in 77 operated patients. J. Clin. Endocrinol. Metab. 94, 1713–1722 (2009).

    Article  CAS  PubMed  Google Scholar 

  24. Sundin, A. Imaging of adrenal masses with emphasis on adrenocortical tumors. Theranostics 2, 516–522 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Hahner, S. et al. [123I]Iodometomidate for molecular imaging of adrenocortical cytochrome P450 family 11B enzymes. J. Clin. Endocrinol. Metab. 93, 2358–2365 (2008).

    Article  CAS  PubMed  Google Scholar 

  26. Mackie, G. C. et al. Use of [18F]fluorodeoxyglucose positron emission tomography in evaluating locally recurrent and metastatic adrenocortical carcinoma. J. Clin. Endocrinol. Metab. 91, 2665–2671 (2006).

    Article  CAS  PubMed  Google Scholar 

  27. Leboulleux, S. et al. Diagnostic and prognostic value of 18-fluorodeoxyglucose positron emission tomography in adrenocortical carcinoma: a prospective comparison with computed tomography. J. Clin. Endocrinol. Metab. 91, 920–925 (2006).

    Article  CAS  PubMed  Google Scholar 

  28. Khan, T. S. et al. 11C-metomidate PET imaging of adrenocortical cancer. Eur. J. Nucl. Med. Mol. Imaging 30, 403–410 (2003).

    Article  PubMed  Google Scholar 

  29. Yang, Z. G. et al. Differentiation between tuberculosis and primary tumors in the adrenal gland: evaluation with contrast enhanced CT. Eur. Radiol. 16, 2031–2036 (2006).

    Article  PubMed  Google Scholar 

  30. Liatsikos, E. N. et al. Primary adrenal tuberculosis: role of computed tomography and CT-guided biopsy in diagnosis. Urol. Int. 76, 285–287 (2006).

    Article  CAS  PubMed  Google Scholar 

  31. Guo, Y. K. et al. Addison's disease due to adrenal tuberculosis: contrast-enhanced CT features and clinical duration correlation. Eur. J. Radiol. 62, 126–131 (2007).

    Article  PubMed  Google Scholar 

  32. Ma, E. S. et al. Tuberculous Addison's disease: morphological and quantitative evaluation with multidetectorrow CT. Eur. J. Radiol. 62, 352–358 (2007).

    Article  PubMed  Google Scholar 

  33. Kumar, N., Singh, S. & Govil, S. Adrenal histoplasmosis: clinical presentation and imaging features in nine cases. Abdom. Imaging 28, 703–708 (2003).

    Article  CAS  PubMed  Google Scholar 

  34. Zhang, L. J., Yang, G. F., Shen, W. & Qi, J. Imaging of primary adrenal lymphoma: case report and literature review. Acta Radiol. 47, 993–997 (2006).

    Article  CAS  PubMed  Google Scholar 

  35. Galati, S. J., Hopkins, S. M., Cheesman, K. C., Zhuk, R. A. & Levine, A. C. Primary aldosteronism: emerging trends. Trends Endocrinol. Metab. 24, 421–430 (2013).

    Article  CAS  PubMed  Google Scholar 

  36. Stowasser, M., Primary aldosteronism in 2011: Towards a better understanding of causation and consequences. Nat. Rev. Endocrinol. 8, 70–72 (2011).

    Article  PubMed  CAS  Google Scholar 

  37. Nwariaku, F. E. et al. Primary hyperaldosteronism, effect of adrenal vein sampling on surgical outcome. Arch. Surg. 141, 497–503 (2006).

    Article  PubMed  Google Scholar 

  38. White, M. L. et al. The role of radiologic studies in the evaluation and management of primary hyperaldosteronism. Surgery 144, 926–933 (2008).

    Article  PubMed  Google Scholar 

  39. Webb, R. et al. What is the best criterion for the interpretation of adrenal vein sample results in patients with primary hyperaldosteronism? Ann. Surg. Oncol. 19, 1881–1886 (2012).

    Article  PubMed  Google Scholar 

  40. Magill, S. B. et al. Comparison of adrenal vein sampling and computed tomography in the differentiation of primary aldosteronism. J. Clin. Endocr. Metabol. 86, 1066–1071 (2001).

    CAS  Google Scholar 

  41. Lingam, R. K. et al. CT of primary hyperaldosteronism (Conn's Syndrome): the value of measuring the adrenal gland. AJR Am. J. Roentgenol. 181, 843–849 (2003).

    Article  CAS  PubMed  Google Scholar 

  42. Harvey, A., Kline, G. & Pasieka, J. L. Adrenal venous sampling in primary hyperaldosteronism: comparison of radiographic with biochemical success and the clinical decision- making with ''less than ideal'' testing. Surgery 140, 847–855 (2006).

    Article  PubMed  Google Scholar 

  43. Espiner, E. A., Ross, D. G., Yandle, T. G., Richards, A. M. & Hunt, P. J. Predicting surgically remedial primary aldosteronism: role of adrenal scanning, posture testing, and adrenal vein sampling. J. Clin. Endocr. Metabol. 88, 3637–3644 (2003).

    Article  CAS  Google Scholar 

  44. Doppman, J. L. & Gill, J. R. Hyperaldosteronism: sampling and adrenal veins. Radiology 198, 309–312 (1996).

    Article  CAS  PubMed  Google Scholar 

  45. Tan, Y. Y. et al. Selective use of adrenal venous sampling in the lateralization of aldosterone-producing adenomas. World J. Surg. 30, 879–885 (2006).

    Article  PubMed  Google Scholar 

  46. Young, W. F. et al. Role for adrenal venous sampling in primary aldosteronism. Surgery 136, 1227–1235 (2004).

    Article  PubMed  Google Scholar 

  47. Rossi, G. P. et al. An expert consensus statement on use of adrenal vein sampling for the subtyping of primary aldosteronism. Hypertension 63, 151–160 (2014).

    Article  CAS  PubMed  Google Scholar 

  48. Harvey, A., Kline, G. & Pasieka, J. L. Adrenal venous sampling in primary hyperaldosteronism: comparison of radiographic with biochemical success and the clinical decision-making with “less than ideal” testing. Surgery 140, 847–853 (2006).

    Article  PubMed  Google Scholar 

  49. Sacks, B. A., Brook, O. R. & Brennan, I. M., Adrenal venous sampling: promises and pitfalls. Curr. Opin. Endocrinol. Diabetes Obes. 20, 180–185 (2013).

    Article  PubMed  Google Scholar 

  50. Kline, G. A. et al. Adrenal vein sampling may not be a gold-standard diagnostic test in primary aldosteronism: final diagnosis depends upon which interpretation rule is used. Variable interpretation of adrenal vein sampling. Int. Urol. Nephrol. 40, 1035–1043 (2008).

    Article  CAS  PubMed  Google Scholar 

  51. Webb, R. et al. What is the best criterion for the interpretation of adrenal vein sample results in patients with primary hyperaldosteronism? Ann. Surg. Oncol. 19, 1881–1886 (2012).

    Article  PubMed  Google Scholar 

  52. Burton, T. J. et al. (PET)-CT for lateralizing aldosterone secretion by Conn's adenomas. J. Clin. Endocrinol. Metab. 97, 100–109 (2012).

    Article  CAS  PubMed  Google Scholar 

  53. Zarnegar, R. et al. The aldosteronoma resolution score: predicting complete resolution of hypertension after adrenalectomy for aldosteronoma. Ann. Surg. 247, 511–518 (2008).

    Article  PubMed  Google Scholar 

  54. Nieman, L. K. et al. The diagnosis of Cushing's syndrome: an Endocrine Society clinical practice guideline. J. Clin. Endocrinol. Metab. 93, 1526–1540 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Tritos, N. A., Biller, B. M. & Swearingen, B. Management of Cushing disease. Nat. Rev. Endocrinol. 7, 279–289 (2011).

    Article  CAS  PubMed  Google Scholar 

  56. Arnaldi, G. et al. Diagnosis and complications of Cushing's syndrome: a consensus statement. J. Clin. Endocrinol. Metab. 88, 5593–5602 (2003).

    Article  CAS  PubMed  Google Scholar 

  57. Turpeinen, U., Markkanen, H., Välimaki, M. & Stenman, U. H. Determination of urinary free cortisol by HPLC. Clin. Chem. 43, 1386–1391 (1997).

    Article  CAS  PubMed  Google Scholar 

  58. Young, W. F. Jr. Clinical practice: the incidentally discovered adrenal mass. N. Engl. J. Med. 356, 601–610 (2007).

    Article  CAS  PubMed  Google Scholar 

  59. De Leo, M. et al. Subclinical Cushing's syndrome. Best Pract. Res. Clin. Endocrinol. Metab. 26, 497–505 (2012).

    Article  CAS  PubMed  Google Scholar 

  60. Morelli, V. et al. Bilateral and unilateral adrenal incidentalomas: biochemical and clinical characteristics. Eur. J. Endocrinol. 168, 235–241 (2013).

    Article  CAS  PubMed  Google Scholar 

  61. Eller-Vainicher, C. et al. Accuracy of several parameters of hypothalamic–pituitary–adrenal axis in predicting before surgery the metabolic effects of the removal of adrenal incidentaloma. Eur. J. Endocrinol. 163, 925–935 (2010).

    Article  CAS  PubMed  Google Scholar 

  62. Chiodini, I. Diagnosis and treatment of subclinical hypercortisolism. J. Clin. Enocrinol. Metabol. 96, 1223–1236 (2010).

    Article  CAS  Google Scholar 

  63. Akehi, Y. et al. Proposed diagnostic criteria for subclinical Cushing's syndrome associated with adrenal incidentaloma. Endocr. J. 60, 903–912 (2013).

    Article  CAS  PubMed  Google Scholar 

  64. Chiodini, I. Clinical review: Diagnosis and treatment of subclinical hypercortisolism. J. Clin. Endocrinol. Metab. 96, 1223–1236 (2011).

    Article  CAS  PubMed  Google Scholar 

  65. Guerrieri, M. et al. Primary adrenal hypercortisolism: minimally invasive surgical treatment or medical therapy? A retrospective study with longterm follow-up evaluation. Surg. Endosc. 24, 2542–2546 (2010).

    Article  PubMed  Google Scholar 

  66. Mauclère-Denost, S. et al. Surgical excision of subclinical cortisol secreting incidentalomas: impact on blood pressure, BMI and glucose metabolism. Ann. Endocrinol. 70, 211–217 (2009).

    Article  CAS  Google Scholar 

  67. Toniato, A. et al. Surgical versus conservative management for subclinical Cushing syndrome in adrenal incidentalomas: a prospective randomized study. Ann. Surg. 249, 388–391 (2009).

    Article  PubMed  Google Scholar 

  68. Chiodini, I. et al. Beneficial metabolic effects of prompt surgical treatment in patients with an adrenal incidentaloma causing biochemical hypercortisolism. J. Clin. Endocrinol. Metab. 95, 2736–2745 (2010).

    Article  CAS  PubMed  Google Scholar 

  69. Mitchell, I. C. et al. “Subclinical Cushing's syndrome” is not subclinical: improvement after adrenalectomy in 9 patients. Surgery 142, 900–905 (2007).

    Article  PubMed  Google Scholar 

  70. Taskin, H. E., Siperstein, A., Mercan, S. & Berber, E. Laparoscopic posterior retroperitoneal adrenalectomy. J. Surg. Oncol. 106, 619–621 (2012).

    Article  PubMed  Google Scholar 

  71. Callender, G. G. et al. Posterior retroperitoneoscopic adrenalectomy. Adv. Surg. 43, 147–157 (2009).

    Article  PubMed  Google Scholar 

  72. Dickson, P. V. et al. Posterior retroperitoneoscopic adrenalectomy: a contemporary American experience. J. Am. Coll. Surg. 212, 659–665 (2011).

    Article  PubMed  Google Scholar 

  73. Elfenbein, D. M., Scarborough, J. E., Speicher, P. J. & Scheri, R. P. Comparison of laparoscopic versus open adrenalectomy: results from American College of Surgeons-National Surgery Quality Improvement Project. J. Surg. Res. 184, 216–220 (2013).

    Article  PubMed  Google Scholar 

  74. Bittner, J. G. 4th, Gershuni, V. M., Matthews, B. D., Moley, J. F. & Brunt, L. M. Risk factors affecting operative approach, conversion, and morbidity for adrenalectomy: a single-institution series of 402 patients. Surg. Endosc. 27, 2342–2350 (2013).

    Article  PubMed  Google Scholar 

  75. Walz, M. K. et al. Endoscopic treatment of large primary adrenal tumours. Br. J. Surg. 92, 719–723 (2005).

    Article  CAS  PubMed  Google Scholar 

  76. Carter, Y. M., Mazeh, H., Sippel, R. S. & Chen, H. Safety and feasibility of laparoscopic resection for large (≥6 cm) pheochromocytomas without suspected malignancy. Endocr. Pract. 18, 720–726 (2012).

    Article  PubMed  PubMed Central  Google Scholar 

  77. Zografos, G. N. et al. Laparoscopic resection of large adrenal tumors. JSLS 14, 364–368 (2010).

    Article  PubMed  PubMed Central  Google Scholar 

  78. Boylu, U., Oommen, M., Lee, B. R. & Thomas, R. Laparoscopic adrenalectomy for large adrenal masses: pushing the envelope. J. Endourol. 23, 971–975 (2009).

    Article  PubMed  Google Scholar 

  79. Castillo, O. A., Vitagliano, G., Secin, F. P., Kerkebe, M. & Arellano, L. Laparoscopic adrenalectomy for adrenal masses: does size matter? Urology 71, 1138–1141 (2008).

    Article  PubMed  Google Scholar 

  80. Mercan, S., Seven, R., Ozarmagan, S. & Tezelman, S. Endoscopic retroperitoneal adrenalectomy. Surgery 118, 1071–1075 (1995).

    Article  CAS  PubMed  Google Scholar 

  81. Walz, M. K. Posterior retroperitoneoscopic adrenalectomy—results of 560 procedures in 520 patients. Surgery 140, 943–948 (2006).

    Article  PubMed  Google Scholar 

  82. Barczynski, M. et al. Posterior retroperitoneoscopic adrenalectomy: a comparison between the initial experience in the invention phase and introductory phase of the new surgical technique. World J. Surg. 31, 65–71 (2007).

    Article  PubMed  Google Scholar 

  83. Walz, M. K. & Alesina, P. F. Single access retroperitoneoscopic adrenalectomy (SARA)--one step beyond in endocrine surgery. Langenbecks Arch. Surg. 394, 447–450 (2009).

    Article  PubMed  Google Scholar 

  84. Walz, M. K. et al. Posterior retroperitoneoscopic adrenalectomy: lessons learned within five years. World J. Surg. 25, 728–734 (2001).

    Article  CAS  PubMed  Google Scholar 

  85. Walz, M. K. et al. Posterior retroperitoneoscopy as a new minimally invasive approach for adrenalectomy: results of 30 adrenalectomies in 27 patients. World J. Surg. 20, 769–774 (1996).

    Article  CAS  PubMed  Google Scholar 

  86. Giebler, R. M., Walz, M. K., Peitgen, K. & Scherer, R. U. Hemodynamic changes after retroperitoneal CO2 insufflation for posterior retroperitoneoscopic adrenalectomy. Anesth. Analg. 82, 827–831 (1996).

    CAS  PubMed  Google Scholar 

  87. Agcaoglu, O., Sahin, D. A., Siperstein, A. & Berber, E. Selection algorithm for posterior versus lateral approach in laparoscopic adrenalectomy. Surgery 151, 731–735 (2012).

    Article  PubMed  Google Scholar 

  88. Berber, E., Mitchell, J., Milas, M. & Siperstein, A. Robotic posterior retroperitoneal adrenalectomy: operative technique. Arch. Surg. 145, 781–784 (2010).

    Article  PubMed  Google Scholar 

  89. Agcaoglu, O., Aliyev, S., Karabulut, K., Siperstein, A. & Berber, E. Robotic vs laparoscopic posterior retroperitoneal adrenalectomy. Arch. Surg. 147, 272–275 (2012).

    Article  PubMed  Google Scholar 

  90. Agcaoglu, O. et al. Robotic versus laparoscopic resection of large adrenal tumors. Ann. Surg. Oncol. 19, 2288–2294 (2012).

    Article  PubMed  Google Scholar 

  91. Morris, L. F. & Perrier, N. D. Advances in robotic adrenalectomy. Curr. Opin. Oncol. 24, 1–6 (2012).

    Article  PubMed  Google Scholar 

  92. Dickson, P. V. et al. Robotic-assisted retroperitoneoscopic adrenalectomy: making a good procedure even better. Am. Surg. 79, 84–89 (2013).

    Article  PubMed  Google Scholar 

  93. Park, J. H. et al. Robot-assisted posterior retroperitoneoscopic adrenalectomy: single port access. J. Korean Surg. Soc. 81 (Suppl. 1), S21–S24 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  94. Taskin, H. E., Arslan, N. C., Aliyev, S. & Berber, E. Robotic endocrine surgery: state of the art. World J. Surg. 37, 2731–2739 (2013).

    Article  PubMed  Google Scholar 

  95. Garcia, L. J., Avella, D. M., Hartman, B., Kimchi, E. & Staveley-O'Carroll, K. F. Thoracoabdominal incision: a forgotten tool in the management of complex upper gastrointestinal complications. Am. J. Surg. 197, e28–e31 (2009).

    Article  PubMed  Google Scholar 

  96. Brauckhoff, M. et al. Limitations of intraoperative adrenal remnant volume measurement in patients undergoing subtotal adrenalectomy. World J. Surg. 32, 863–872 (2008).

    Article  PubMed  Google Scholar 

  97. Walz, M. K. Extent of adrenalectomy for adrenal neoplasm: cortical sparing (subtotal) versus total adrenalectomy. Surg. Clin. North Am. 84, 743–753 (2004).

    Article  PubMed  Google Scholar 

  98. Alesina, P. F. et al. Minimally invasive cortical-sparing surgery for bilateral pheochromocytomas. Langenbecks Arch. Surg. 397, 233–238 (2012).

    Article  PubMed  Google Scholar 

  99. Ritzel, K. et al. Outcome of bilateral adrenalectomy in Cushing's syndrome: A systematic review. J. Clin. Endocrinol. Metab. 98, 3939–3948 (2013).

    Article  CAS  PubMed  Google Scholar 

  100. Cheng, S. P., Saunders, B. D., Gauger, P. G. & Doherty, G. M. Laparoscopic partial adrenalectomy for bilateral pheochromocytomas. Ann. Surg. Oncol. 15, 2506–2508 (2008).

    Article  PubMed  Google Scholar 

  101. Walz, M. K. et al. Endoscopic treatment of recurrent phaeochromocytomas and retroperitoneal paragangliomas. European Surgeon 35, 93–96 (2003).

    Article  Google Scholar 

  102. Sparagana, M. Late recurrence of benign pheochromocytomas: the necessity for long-term follow-up. J. Surg. Oncol. 37, 140–146 (1988).

    Article  CAS  PubMed  Google Scholar 

  103. Nakada, T. et al. Therapeutic outcome of primary aldosteronism: adrenalectomy versus enucleation of aldosterone producing adenoma. J. Urol. 153, 1775–1780 (1995).

    Article  CAS  PubMed  Google Scholar 

  104. Kok, K. Y. & Yapp, S. K. Laparoscopic adrenal-sparing surgery for primary hyperaldosteronism due to aldosterone-producing adenoma. Surg. Endosc. 16, 108–111 (2002).

    Article  CAS  PubMed  Google Scholar 

  105. Sasagawa, I. et al. Posterior retroperitoneoscopic partial adrenalectomy using ultrasonic scalpel for aldosterone producing adenoma. J. Endourol. 14, 573–576 (2000).

    Article  CAS  PubMed  Google Scholar 

  106. Fendrich, V., Ramaswamy, A. & Nies, C. Hyperaldosteronism persisting after subtotal adrenalectomy. Chirurg 74, 473–477 (2003).

    Article  CAS  PubMed  Google Scholar 

  107. Alesina, P. F. et al. Posterior retroperitoneoscopic adrenalectomy for clinical and subclinical Cushing's syndrome. World J. Surg. 34, 1391–1397 (2010).

    Article  PubMed  Google Scholar 

  108. Berruti, A. et al. Adrenal cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 23 (Suppl. 7), 131–138 (2012).

    Article  Google Scholar 

  109. Fassnacht, M., Kroiss, M. & Allolio, B. Update in adrenocortical carcinoma. J. Clin. Endocrinol. Metab. 98, 4551–4564 (2013).

    Article  CAS  PubMed  Google Scholar 

  110. Else, T. et al. Adrenocortical carcinoma. Endocr. Rev. http://dx.doi.org/10.1210/er.2013-1029.

  111. Lombardi, C. P. Adrenocortical carcinoma: effect of hospital volume on patient outcome. Langenbecks Arch. Surg. 397, 201–207 (2012).

    Article  PubMed  Google Scholar 

  112. Guerrieri, M. et al. The learning curve in laparoscopic adrenalectomy. J. Endocrinol. Invest. 31, 531–536 (2008).

    Article  CAS  PubMed  Google Scholar 

  113. Park, H. S., Roman, S. A. & Sosa, J. A. Outcomes from 3144 adrenalectomies in the United States: which matters more, surgeon volume or specialty? Arch. Surg. 144, 1060–1067 (2009).

    Article  PubMed  Google Scholar 

  114. Schteingart, D. E. Management of patients with adrenal cancer: recommendations of an international consensus conference. Endocr. Relat. Cancer 12, 667–680 (2005).

    Article  CAS  PubMed  Google Scholar 

  115. Henry, J. F., Peix, J. L. & Kraimps, J. L. Positional statement of the European Society of Endocrine Surgeons (ESES) on malignant adrenal tumors. Langenbecks Arch. Surg. 397, 145–146 (2012).

    Article  PubMed  Google Scholar 

  116. Berruti, A. et al. Adrenal cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 23 (Suppl. 7), 131–138 (2012).

    Article  Google Scholar 

  117. Gonzalez, R. J. et al. Laparoscopic resection of adrenal cortical carcinoma: a cautionary note. Surgery 138, 1078–1085 (2005).

    Article  PubMed  Google Scholar 

  118. Grubbs, E. G. et al. Recurrence of adrenal cortical carcinoma following resection: surgery alone can achieve results equal to surgery plus mitotane. Ann. Surg. Oncol. 17, 263–270 (2010).

    Article  PubMed  Google Scholar 

  119. Leboulleux, S. et al. Adrenocortical carcinoma: is the surgical approach a risk factor of peritoneal carcinomatosis? Eur. J. Endocrinol. 162, 1147–1153 (2010).

    Article  CAS  PubMed  Google Scholar 

  120. Porpiglia, F. et al. Retrospective evaluation of the outcome of open versus laparoscopic adrenalectomy for stage I and II adrenocortical cancer. Eur. Urol. 57, 873–878 (2010).

    Article  PubMed  Google Scholar 

  121. Lombardi, C. P. et al. Open versus endoscopic adrenalectomy in the treatment of localized (stage I/II) adrenocortical carcinoma: Results of a multi-institutional Italian survey. Surgery 152, 1158–1164 (2012).

    Article  PubMed  Google Scholar 

  122. Brix, D. et al. Laparoscopic versus open adrenalectomy for adrenocortical carcinoma: surgical and oncologic outcome in 152 patients. Eur. Urol. 58, 609–615 (2010).

    Article  PubMed  Google Scholar 

  123. Miller, B. S. et al. Laparoscopic resection is inappropriate in patients with known or suspected adrenocortical carcinoma. World J. Surg. 34, 1380–1385 (2010).

    Article  CAS  PubMed  Google Scholar 

  124. Miller, B. S., Gauger, P. G., Hammer, G. D. & Doherty, G. M. Resection of adrenocortical carcinoma is less complete and local recurrence occurs sooner and more often after laparoscopic adrenalectomy than after open adrenalectomy. Surgery 152, 1150–1157 (2012).

    Article  PubMed  Google Scholar 

  125. Reibetanz, J. Impact of lymphadenectomy on the oncologic outcome of patients with adrenocortical carcinoma. Ann. Surg. 255, 363–369 (2012).

    Article  PubMed  Google Scholar 

  126. Miller, B. S. & Doherty, G. M. Regional lymphadenectomy for adrenocortical carcinoma. Ann. Surg. 257, e13–e14 (2013).

    Article  PubMed  Google Scholar 

  127. Gaujoux, S. & Brennan, M. F. Recommendation for standardized surgical management of primary adrenocortical carcinoma. Surgery 152, 123–132 (2012).

    Article  PubMed  Google Scholar 

  128. Ekici, S. & Ciancio, G. Surgical management of large adrenal masses with or without thrombus extending into the inferior vena cava. J. Urol. 172, 2340–2343 (2004).

    Article  PubMed  Google Scholar 

  129. Assié, G. et al. Prognostic parameters of metastatic adrenocortical carcinoma. J. Clin. Endocrinol. Metab. 92, 148–154 (2007).

    Article  CAS  PubMed  Google Scholar 

  130. Erdogan, I. et al. The role of surgery in the management of recurrent adrenocortical carcinoma. J. Clin. Endocrinol. Metab. 98, 181–191 (2013).

    Article  CAS  PubMed  Google Scholar 

  131. Bellantone, R. et al. Role of reoperation in recurrence of adrenal cortical carcinoma: results from 188 cases collected in the Italian National Registry for Adrenal Cortical Carcinoma. Surgery 122, 1212–1218 (1997).

    Article  CAS  PubMed  Google Scholar 

  132. Schulick, R. D. & Brennan, M. F. Long-term survival after complete resection and repeat resection in patients with adrenocortical carcinoma. Ann. Surg. Oncol. 6, 719–726 (1999).

    Article  CAS  PubMed  Google Scholar 

  133. Miller, B. S., Gauger, P. G., Hammer, G. D., Giordano, T. J. & Doherty, G. M. Proposal for modification of the ENSAT staging system for adrenocortical carcinoma using tumor grade. Langenbecks Arch. Surg. 395, 955–961 (2010).

    Article  PubMed  Google Scholar 

  134. Dy, B. M. et al. Operative intervention for recurrent adrenocortical cancer. Surgery 154, 1292–1299 (2013).

    Article  PubMed  Google Scholar 

  135. Kazaure, H. S., Roman, S. A. & Sosa, J. A. Adrenalectomy in older Americans has increased morbidity and mortality: an analysis of 6,416 patients. Ann. Surg. Oncol. 18, 2714–2721 (2011).

    Article  PubMed  Google Scholar 

  136. Kazaure, H. S., Roman, S. A. & Sosa, J. A. Obesity is a predictor of morbidity in 1,629 patients who underwent adrenalectomy. World J. Surg. 35, 1287–1295 (2011).

    Article  PubMed  Google Scholar 

  137. Doherty, G. M., Nieman, L. K., Cutler, G. B. Jr, Chrousos, G. P. & Norton, J. A. Time to recovery of the hypothalamic–pituitary–adrenal axis after curative resection of adrenal tumors in patients with Cushing's syndrome. Surgery 108, 1085–1090 (1990).

    CAS  PubMed  Google Scholar 

  138. Sippel, R. S. et al. Waiting for change: symptom resolution after adrenalectomy for Cushing's syndrome. Surgery 144, 1054–1060 (2008).

    Article  PubMed  Google Scholar 

  139. Ragnarsson, O. & Johannsson, G. Cushing's syndrome: a structured short- and long-term management plan for patients in remission. Eur. J. Endocrinol. 169, R139–R152 (2013).

    Article  CAS  PubMed  Google Scholar 

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B.S.M. researched data for the article, contributed to discussion of the content and wrote the article. G.M.D. reviewed/edited the manuscript before submission.

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Correspondence to Barbra S. Miller.

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Miller, B., Doherty, G. Surgical management of adrenocortical tumours. Nat Rev Endocrinol 10, 282–292 (2014). https://doi.org/10.1038/nrendo.2014.26

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