Sima Oana-Claudia, Costachescu Mihai, Valea Ana, Stanciu Mihaela, Lebada Ioana Codruta, Nistor Tiberiu Vasile Ioan, Ciobica Mihai-Lucian, Nistor Claudiu, Carsote Mara
PhD Doctoral School of "Carol Davila" University of Medicine and Pharmacy, 010825 Bucharest, Romania.
Department of Radiology and Medical Imaging, Fundeni Clinical Institute, 022328 Bucharest, Romania.
Diseases. 2025 May 26;13(6):169. doi: 10.3390/diseases13060169.
Adrenal incidentalomas are detected in various medical and surgical healthcare departments, including primary healthcare. One up to three out of ten individuals confirmed with nonfunctioning adrenal incidentalomas (NFAs) actually present a mild autonomous cortisol secretion (MACS), which is distinct from Cushing's syndrome.
We aimed to assess the cortisol secretion in newly detected adrenal incidentalomas in patients who were referred by their primary healthcare physician upon accidental detection of an adrenal tumor at abdominal computed tomography (CT) scan that was performed for unrelated (non-endocrine) purposes.
This retrospective study included adults diagnosed with an adrenal incidentaloma via CT during the previous 3 months.
age ≥ 40 years (y). A triple stratification of exclusion criteria involved: (1) Clinical aspects and medical records such as active malignancies or malignancies under surveillance protocols, subjects under exogenous glucocorticoid exposure (current or during the previous year), or suggestive endocrine phenotypes for any hormonal ailment; (2) Radiological appearance of suspected/confirmed (primary or secondary) adrenal malignancy, adrenal cysts, or myelolipomas; (3) Endocrine assays consistent with active endocrine tumors. Protocol of assessment included baseline ACTH, morning plasma cortisol (C-B), cortisol at 6 p.m. (C-6 pm), and after 1 mg dexamethasone suppression testing (C-1 mg-DST), 24-h urinary free cortisol (UFC), and a second opinion for all CT scans. MACS were defined based on C-1 mg-DST ≥ 1.8 and <5 µg/dL (non-MACS: C-1 mg-DST < 1.8 µg/dL).
The cohort (N = 60, 78.33% female; 60.72 ± 10.62 y) associated high blood pressure (HBP) in 66.67%, respectively, type 2 diabetes (T2D) in 28.37% of the patients. Females were statistically significantly older than males (62.40 ± 10.47 vs. 54.62 ± 9.11 y, = 0.018), while subjects with unilateral vs. bilateral tumors (affecting 26.67% of the individuals) and those with MACS-positive vs. MACS-negative profile had a similar age. Body mass index (BMI) was similar between patients with unilateral vs. bilateral incidentalomas, regardless of MACS. Patients were divided into five age groups (decades); most of them were found between 60 and 69 years (40%). Left-gland involvement was found in 43.33% of all cases. The mean largest tumor diameter was 26.08 ± 8.78 mm. The highest rate of bilateral tumors was 46.67% in the 50-59 y decade. The rate of unilateral/bilateral and tumor diameters was similar in females vs. males. The MACS-positive rate was similar in females vs. males (23.40% vs. 23.08%). A statistically significant negative correlation (N = 60) was found between BMI and C-B (r = -0.193, = 0.03) and BMI and UFC (r = -0.185, = 0.038), and a positive correlation was found between C-B and C-6 pm (r = 0.32, < 0.001), C-B and UFC (r = 0.226, = 0.011), and C-6 pm and C-1 mg-DST (r = 0.229, = 0.010), and the largest tumor diameter and C-1 mg-DST (r = 0.241, = 0.007).
Adrenal incidentalomas belong to a complex scenario of detection in the modern medical era, requiring a multidisciplinary collaboration since the patients might be initially detected in different departments (as seen in the current study) and then referred to primary healthcare for further decision. In these consecutive patients, we found a higher female prevalence, a MACS rate of 23.33%, regardless of uni/bilateral involvement or gender distribution, and a relatively high rate (than expected from general data) of bilateral involvement of 26.67%. The MACS-positive profile adds to the disease burden and might require additional assessments during follow-up and a protocol of surveillance, including a tailored decision of tumor removal. The identification of an adrenal incidentaloma at CT and its hormonal characterization needs to be integrated into the panel of various chronic disorders of one patient. The collaboration between endocrinologists and primary healthcare physicians might improve the overall long-term outcomes.
肾上腺偶发瘤在包括基层医疗保健在内的各个医疗和外科保健科室中均有发现。在确诊为无功能肾上腺偶发瘤(NFA)的患者中,每十人中就有一至三人实际上存在轻度自主性皮质醇分泌(MACS),这与库欣综合征不同。
我们旨在评估因腹部计算机断层扫描(CT)意外发现肾上腺肿瘤(该扫描是为无关的(非内分泌)目的进行的)而由基层医疗医生转诊的患者中新发现的肾上腺偶发瘤的皮质醇分泌情况。
这项回顾性研究纳入了在过去3个月内通过CT诊断为肾上腺偶发瘤的成年人。
年龄≥40岁(y)。排除标准的三重分层包括:(1)临床情况和病历,如活跃的恶性肿瘤或处于监测方案下的恶性肿瘤、接受外源性糖皮质激素治疗的受试者(当前或前一年),或任何激素疾病的提示性内分泌表型;(2)疑似/确诊(原发性或继发性)肾上腺恶性肿瘤、肾上腺囊肿或髓样脂肪瘤的放射学表现;(3)与活跃的内分泌肿瘤一致的内分泌检测。评估方案包括基线促肾上腺皮质激素(ACTH)、上午血浆皮质醇(C-B)、下午6点的皮质醇(C-6 pm)、1毫克地塞米松抑制试验后(C-1 mg-DST)、24小时尿游离皮质醇(UFC),以及对所有CT扫描的二次评估。MACS的定义基于C-1 mg-DST≥1.8且<5μg/dL(非MACS:C-1 mg-DST<1.8μg/dL)。
该队列(N = 60,78.33%为女性;60.72±10.62岁)中,分别有66.67%的患者患有高血压(HBP),28.37%的患者患有2型糖尿病(T2D)。女性在统计学上比男性年龄大(62.40±10.47岁对54.62±9.11岁,P = 0.018),而单侧与双侧肿瘤患者(占个体的26.67%)以及MACS阳性与MACS阴性患者的年龄相似。无论MACS如何,单侧与双侧偶发瘤患者的体重指数(BMI)相似。患者分为五个年龄组(十年);大多数患者年龄在60至69岁之间(40%)。在所有病例中,43.33%的病例左侧肾上腺受累。肿瘤最大平均直径为26.08±8.78毫米。在50至59岁的十年中,双侧肿瘤的发生率最高,为46.67%。女性与男性的单侧/双侧肿瘤发生率和肿瘤直径相似。女性与男性的MACS阳性率相似(23.40%对23.08%)。在BMI与C-B之间(r = -0.193,P = 0.03)以及BMI与UFC之间(r = -0.185,P = 0.038)发现了具有统计学意义的负相关,在C-B与C-6 pm之间(r = 0.32,P<0.001)、C-B与UFC之间(r = 0.226,P = 0.011)、C-6 pm与C-1 mg-DST之间(r =