1.Clinical characteristics and follow-up of Korean patients with adrenal incidentalomas.
Yoon Young CHO ; Sunghwan SUH ; Ji Young JOUNG ; Hyemin JEONG ; Dongmo JE ; Hongseok YOO ; Taek Kyu PARK ; Yong Ki MIN ; Kwang Won KIM ; Jae Hyeon KIM
The Korean Journal of Internal Medicine 2013;28(5):557-564
BACKGROUND/AIMS: We investigated the clinical characteristics and follow-up findings of subjects with adrenal incidentalomas in a single, tertiary-care hospital in South Korea. METHODS: The study consisted of a retrospective analysis of 282 adrenal incidentaloma patients who underwent radiographic and endocrinological evaluations at Samsung Medical Center in Seoul, South Korea, between January 2004 and July 2011. RESULTS: Most (86.2%) of the subjects were found to have nonfunctioning tumors. Functioning tumors were seen in 39 patients (13.8%). Among them, 28 (9.9%) had subclinical Cushing syndrome (SCS), six (2.1%) had pheochromocytoma, and five (1.8%) had primary hyperaldosteronism. Malignant adrenal tumors were discovered in three cases: two (0.7%) were primary adrenal cancers, and one (0.4%) was a secondary metastasis from a lung cancer. Significant risk factors for functional tumors were female gender (odds ratio [OR], 3.386; 95% confidence interval [CI], 1.611 to 7.117; p = 0.0013) and a noncontrast attenuation value of > 10 Hounsfield units (OR, 2.806; 95% CI, 1.231 to 6.397; p = 0.0141). During follow-up (mean, 22.5 months) of 72 of the patients, three (4.2%) developed hormonal changes due to functional tumors. One was confirmed as pheochromocytoma by histopathology, and the others were diagnosed with SCS and followed routinely without surgical intervention. No malignant transformation was found in these patients. CONCLUSIONS: Based on these findings, initial hormonal and radiographic evaluations for adrenal incidentalomas appear to be more important than follow-up tests because functional or malignant changes are rare.
*Adrenal Gland Neoplasms/blood/diagnosis/epidemiology/therapy
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Aged
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*Cushing Syndrome/blood/diagnosis/epidemiology/therapy
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Disease Progression
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Female
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Hormones/blood
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Humans
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*Hyperaldosteronism/blood/diagnosis/epidemiology/therapy
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Logistic Models
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Male
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Middle Aged
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Odds Ratio
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*Pheochromocytoma/blood/diagnosis/epidemiology/therapy
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Predictive Value of Tests
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Prognosis
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Republic of Korea/epidemiology
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Retrospective Studies
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Risk Factors
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Tertiary Care Centers
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Time Factors
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Tomography, X-Ray Computed
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Tumor Markers, Biological/blood
2.Changes in the clinical manifestations of primary aldosteronism.
Sun Hwa KIM ; Jae Hee AHN ; Ho Cheol HONG ; Hae Yoon CHOI ; Yoon Jung KIM ; Nam Hoon KIM ; Hye Jin YOO ; Hee Young KIM ; Ji A SEO ; Nan Hee KIM ; Sin Gon KIM ; Kyung Mook CHOI ; Sei Hyun BAIK ; Dong Seop CHOI
The Korean Journal of Internal Medicine 2014;29(2):217-225
BACKGROUND/AIMS: Primary aldosteronism (PA) is now widely recognized to have a higher prevalence than was once thought. In view of its increasing prevalence, we compared chronological changes in clinical manifestations of PA according to different times of diagnosis. METHODS: In total, 85 patients diagnosed with PA from January 1986 through March 2012 were reviewed retrospectively, based on their medical records. During two periods-1986 to 2005 and 2006 to 2012-41 and 44 patients, respectively, were diagnosed with PA. We compared the clinical and biological characteristics of PA between these periods. RESULTS: The results demonstrate an increasing trend in the prevalence of idiopathic hyperaldosteronism (IHA; p = 0.19). In the 2006 to 2012 period, patients with PA presented with higher serum potassium levels at the time of diagnosis than in the 1986 to 2005 period (p < 0.0002). Adrenal vein sampling (AVS) was performed mostly in the latter period (82.3%) and the diagnostic accuracy of adrenal computed tomography, compared with AVS, was only 56.2%. About 78.0% versus 86.3% of patients had at least one target organ damage (TOD) in the 1986 to 2005 and 2006 to 2012 periods, respectively (p = 0.39). However, patients with TOD were older and had longer durations of hypertension than patients without, in both periods. CONCLUSIONS: PA is becoming more prevalent. There was an increasing tendency for IHA, and more PA patients presented with normokalemia than in the earlier period. Early and accurate diagnosis of PA with AVS and proper treatment should have substantial prognostic value.
Adrenal Cortex Neoplasms/diagnosis/epidemiology
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Adrenal Glands/radiography
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Adrenocortical Adenoma/diagnosis/epidemiology
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Adult
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Biological Markers/blood
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Female
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Humans
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Hyperaldosteronism/blood/*diagnosis/epidemiology/therapy
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Hyperkalemia/diagnosis/epidemiology
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Hyperplasia
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Hypertension/diagnosis/epidemiology
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Male
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Middle Aged
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Potassium/blood
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Predictive Value of Tests
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Prevalence
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Republic of Korea/epidemiology
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Retrospective Studies
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Risk Factors
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Time Factors
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Tomography, X-Ray Computed
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Treatment Outcome