Clinical, Biochemical, and Radiological Characteristics of a Single-Center Retrospective Cohort of 705 Large Adrenal Tumors
- PMID: 30225430
- PMCID: PMC6124341
- DOI: 10.1016/j.mayocpiqo.2017.11.002
Clinical, Biochemical, and Radiological Characteristics of a Single-Center Retrospective Cohort of 705 Large Adrenal Tumors
Abstract
Objective: To characterize large adrenal tumors (≥4 cm in diameter) and to identify features associated with malignancy.
Patients and methods: We investigated the clinical, biochemical, and imaging characteristics in a large retrospective single-center cohort of patients with adrenal tumors of 4 cm or more in diameter during the period of January 1, 2000, through December 31, 2014.
Results: Of 4085 patients with adrenal tumors, 705 (17%) had adrenal masses measuring 4 cm or more in diameter; of these, 373 (53%) were women, with a median age of 59 years (range, 18-91 years) and median tumor size of 5.2 cm (range, 4.0-24.4 cm). Underlying diagnoses were adrenocortical adenomas (n=216 [31%]), pheochromocytomas (n=158 [22%]), other benign adrenal tumors (n=116 [16%]), adrenocortical carcinomas (n=88 [13%]), and other malignant tumors (n=127 [18%]). Compared with benign tumors, malignant tumors were less frequently diagnosed incidentally (45.5% vs 86.7%), were larger (7 cm [range, 4-24.4 cm] vs 5 cm [range, 4-20 cm]), and had higher unenhanced computed tomographic (CT) attenuation (34.5 Hounsfield units [HU] [range, 14.1-75.5 HU] vs 11.5 HU [range, -110 to 71.3 HU]; P<.001). On multivariate analysis, older age at diagnosis, male sex, nonincidental mode of discovery, larger tumor size, and higher unenhanced CT attenuation were all found to be statistically significant predictors of malignancy.
Conclusion: The prevalence of malignancy in patients with adrenal tumors of 4 cm or more in diameter was 31%. Older age, male sex, nonincidental mode of discovery, larger tumor size, and higher unenhanced CT attenuation were associated with an increased risk for malignancy. Clinical context should guide management in patients with adrenal tumors of 4 cm or more in diameter.
Keywords: ACA, adrenocortical adenoma; ACC, adrenocortical carcinoma; CT, computed tomography; HU, Hounsfield units; OR, odds ratio; PHEO, pheochromocytoma.
Similar articles
-
Presentation and management of patients with adrenal masses: a large tertiary centre experience.Eur J Endocrinol. 2024 Oct 29;191(5):481-490. doi: 10.1093/ejendo/lvae131. Eur J Endocrinol. 2024. PMID: 39425921
-
Not all adrenal incidentalomas require biochemical testing to exclude pheochromocytoma: Mayo clinic experience and a meta-analysis.Gland Surg. 2020 Apr;9(2):362-371. doi: 10.21037/gs.2020.03.04. Gland Surg. 2020. PMID: 32420260 Free PMC article.
-
Incidental Adrenal Nodules in Patients Without Known Malignancy: Prevalence of Malignancy and Utility of Washout CT for Characterization-A Multiinstitutional Study.AJR Am J Roentgenol. 2022 Nov;219(5):804-812. doi: 10.2214/AJR.22.27901. Epub 2022 Jun 22. AJR Am J Roentgenol. 2022. PMID: 35731098
-
Presentation and outcomes of adrenal ganglioneuromas: A cohort study and a systematic review of literature.Clin Endocrinol (Oxf). 2021 Jul;95(1):47-57. doi: 10.1111/cen.14460. Epub 2021 Mar 22. Clin Endocrinol (Oxf). 2021. PMID: 33721367 Free PMC article.
-
Adrenal incidentalomas.Curr Opin Oncol. 2002 Jan;14(1):58-63. doi: 10.1097/00001622-200201000-00011. Curr Opin Oncol. 2002. PMID: 11790982 Review.
Cited by
-
Adrenal tumours in patients with pathogenic APC mutations: a retrospective study.Hered Cancer Clin Pract. 2024 Sep 3;22(1):17. doi: 10.1186/s13053-024-00289-1. Hered Cancer Clin Pract. 2024. PMID: 39227904 Free PMC article.
-
Development and validation of a model predicting adrenal lipid-poor adenoma based on the minimum attenuation value from non-contrast CT: a dual-center retrospective study.BMC Med Imaging. 2024 Aug 12;24(1):210. doi: 10.1186/s12880-024-01392-4. BMC Med Imaging. 2024. PMID: 39134939 Free PMC article.
-
Clinical differences between small and large pheochromocytomas and paragangliomas.Front Endocrinol (Lausanne). 2023 Mar 9;14:1087506. doi: 10.3389/fendo.2023.1087506. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 36967797 Free PMC article.
-
Pheochromocytoma and Adrenocortical Carcinoma: Morphological Characteristics in Endoscopic Ultrasound Imaging.Ultrasound Int Open. 2021 Nov 17;7(2):E64-E70. doi: 10.1055/a-1626-1678. eCollection 2021 Aug. Ultrasound Int Open. 2021. PMID: 34804773 Free PMC article.
-
Characteristics of adrenocortical carcinoma in South Korea: a registry-based nationwide survey.Endocr Connect. 2020 Jun;9(6):519-529. doi: 10.1530/EC-20-0196. Endocr Connect. 2020. PMID: 32438344 Free PMC article.
References
-
- Bovio S., Cataldi A., Reimondo G., et al. Prevalence of adrenal incidentaloma in a contemporary computerized tomography series. J Endocrinol Invest. 2006;29(4):298–302. - PubMed
-
- Song J.H., Chaudhry F.S., Mayo-Smith W.W. The incidental adrenal mass on CT: prevalence of adrenal disease in 1,049 consecutive adrenal masses in patients with no known malignancy. AJR Am J Roentgenol. 2008;190(5):1163–1168. - PubMed
-
- Ciftci A.O., Senocak M.E., Tanyel F.C., Buyukpamukcu N. Adrenocortical tumors in children. J Pediatr Surg. 2001;36(4):549–554. - PubMed
-
- Mayer S.K., Oligny L.L., Deal C., Yazbeck S., Gagné N.N., Blanchard H. Childhood adrenocortical tumors: case series and reevaluation of prognosis–a 24-year experience. J Pediatr Surg. 1997;32(6):911–915. - PubMed
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases