Predictors of recurrence in pheochromocytoma

被引:29
作者
Press, Danielle
Akyuz, Muhammet
Dural, Cem
Aliyev, Shamil
Monteiro, Rosebel
Mino, Jeff
Mitchell, Jamie
Hamrahian, Amir
Siperstein, Allan
Berber, Eren
机构
[1] Cleveland Clin, Dept Endocrine Surg, Cleveland, OH 44106 USA
[2] Cleveland Clin, Dept Endocrinol, Cleveland, OH 44106 USA
关键词
APPARENTLY BENIGN PHEOCHROMOCYTOMA; METASTATIC PHEOCHROMOCYTOMA; SURGICAL RESECTION; FOLLOW-UP; PARAGANGLIOMA; THERAPY;
D O I
10.1016/j.surg.2014.08.044
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. The recurrence rate of pheochromocytoma after adrenalectomy is 6.5-16.5%. This study aims to identify predictors of recurrence and optimal biochemical testing and imaging for detecting the recurrence of pheochromocytoma. Methods. In this retrospective study we reviewed all patients who underwent adrenalectomy for pheochromocytoma during a 14-year period at a single institution. Results. One hundred thirty-five patients had adrenalectomy for pheochromocytoma. Eight patients (6%) developed recurrent disease. The median time from initial operation to diagnosis of recurrence was 35 months. On multivariate analysis, tumor size >5 cm was an independent predictor of recurrence. One patient with recurrence died, 4 had stable disease, 2 had progression of disease, and 1 was cured. Recurrence was diagnosed by increases in plasma and/or urinary metanephrines and positive imaging in 6 patients (75%), and by positive imaging and normal biochemical levels in 2 patients (25%). Conclusion. Patients with large tumors (>5 cm) should be followed vigilantly for recurrence. Because 25% of patients with recurrence had normal biochemical levels, we recommend routine imaging and testing of plasma or urinary metanephrines for prompt diagnosis of recurrence.
引用
收藏
页码:1523 / 1528
页数:6
相关论文
共 14 条
  • [1] Year of diagnosis, features at presentation, and risk of recurrence in patients with pheochromocytoma or secreting paraganglioma
    Amar, L
    Servais, A
    Gimenez-Roqueplo, AP
    Zinzindohoue, F
    Chatellier, G
    Plouin, PF
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (04) : 2110 - 2116
  • [2] Long-term Postoperative Follow-up in Patients with Apparently Benign Pheochromocytoma and Paraganglioma
    Amar, L.
    Fassnacht, M.
    Gimenez-Roqueplo, A. -P.
    Januszewicz, A.
    Prejbisz, A.
    Timmers, H.
    Plouin, P. -F.
    [J]. HORMONE AND METABOLIC RESEARCH, 2012, 44 (05) : 385 - 389
  • [3] Clinical Risk Factors for Malignancy and Overall Survival in Patients with Pheochromocytomas and Sympathetic Paragangliomas: Primary Tumor Size and Primary Tumor Location as Prognostic Indicators
    Ayala-Ramirez, Montserrat
    Feng, Lei
    Johnson, Marcella M.
    Ejaz, Shamim
    Habra, Mouhammed Amir
    Rich, Thereasa
    Busaidy, Naifa
    Cote, Gilbert J.
    Perrier, Nancy
    Phan, Alexandria
    Patel, Shreyaskumar
    Waguespack, Steven
    Jimenez, Camilo
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2011, 96 (03) : 717 - 725
  • [4] PERSISTENT AND RECURRENT PHEOCHROMOCYTOMA - THE ROLE OF SURGERY
    BRENNAN, MF
    KEISER, HR
    [J]. WORLD JOURNAL OF SURGERY, 1982, 6 (04) : 397 - 401
  • [5] Response after Surgical Resection of Metastatic Pheochromocytoma and Paraganglioma: Can Postoperative Biochemical Remission Be Predicted?
    Ellis, Ryan J.
    Patel, Dhaval
    Prodanov, Tamara
    Sadowski, Samira
    Nilubol, Naris
    Adams, Karen
    Steinberg, Seth M.
    Pacak, Karel
    Kebebew, Electron
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS, 2013, 217 (03) : 489 - 496
  • [6] Phase II Study of High-Dose [131I]Metaiodobenzylguanidine Therapy for Patients With Metastatic Pheochromocytoma and Paraganglioma
    Gonias, Sara
    Goldsby, Robert
    Matthay, Katherine K.
    Hawkins, Randall
    Price, David
    Huberty, John
    Damon, Lloyd
    Linker, Charles
    Sznewajs, Aimee
    Shiboski, Steve
    Fitzgerald, Paul
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (25) : 4162 - 4168
  • [7] 131I-Metaiodobenzylguanidine Therapy of Neuroblastoma and Other Neuroendocrine Tumors
    Gruenwald, Frank
    Ezziddin, Samer
    [J]. SEMINARS IN NUCLEAR MEDICINE, 2010, 40 (02) : 153 - 163
  • [8] Management and treatment of pheochromocytomas and paragangliomas
    Mannelli, Massimo
    [J]. PHEOCHROMOCYTOMA, 2006, 1073 : 405 - 416
  • [9] Pheochromocytoma: recommendations for clinical practice from the First International Symposium
    Pacak, Karel
    Eisenhofer, Graeme
    Ahlman, Hakan
    Bornstein, Stefan R.
    Gimenez-Roqueplo, Anne-Paule
    Grossman, Ashley B.
    Kimura, Noriko
    Mannelli, Massimo
    McNicol, Anne Marie
    Tischler, Arthur S.
    [J]. NATURE CLINICAL PRACTICE ENDOCRINOLOGY & METABOLISM, 2007, 3 (02): : 92 - 102
  • [10] Initial work-up and long-term follow-up in patients with phaeochromocytomas and paragangliomas
    Plouin, Pierre-Francois
    Gimenez-Roqueplo, Anne-Paule
    [J]. BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM, 2006, 20 (03) : 421 - 434