Differences in outcomes of bilateral adrenalectomy in patients with ectopic ACTH producing tumor of known and unknown origin

被引:4
|
作者
Yamashita, Thomas Szabo [1 ]
Sada, Alaa [1 ]
Bancos, Irina [2 ]
Young, William F., Jr. [2 ]
Dy, Benzon M. [1 ]
Farley, David R. [1 ]
Lyden, Melanie L. [1 ]
Thompson, Geoffrey B. [1 ]
McKenzie, Travis J. [1 ]
机构
[1] Mayo Clin, Dept Surg, 200 1st St, Rochester, MN 55905 USA
[2] Mayo Clin, Div Endocrinol Diabet Metab & Nutr, 200 1st St, Rochester, MN 55905 USA
来源
AMERICAN JOURNAL OF SURGERY | 2021年 / 221卷 / 02期
关键词
Bilateral adrenalectomy; Ectopic ACTH-Producing tumors; Cushing syndrome; Hypercortisolism; Adrenal gland;
D O I
10.1016/j.amjsurg.2020.08.047
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Endogenous Cushing syndrome (CS) can be caused by ectopic corticotropin-producing tumors of known (EK) and unknown origin (EU). Bilateral adrenalectomy (BA) can be used as definite treatment of hypercortisolism in such cases. This study compared patients undergoing BA for CS secondary to EK vs EU. Methods: Retrospective review (1995-2017) of patients undergoing BA due to EK or EU. We analyzed demographic characteristics, laboratory values, intraoperative variables, surgical outcomes, and survival. Results: 48 patients (26 EU, 22 EK) were identified. Serum cortisol and ACTH concentrations were similar. 92% of BA for EU were performed minimally invasively vs 77% for EK, P = 0.22. Complications occurred in 19% of EU and 4.5% EK, P = 0.2. Mean survival was 4.3 years for EU and 4.0 years for EK without difference in all-cause mortality P = 0.63. Conclusion: BA cure rate was 100% for CS in EU and EK. Morbidity, long term and all-cause mortality differences were not statistically significant between EK and EU. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:460 / 464
页数:5
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