Libè Rossella, Dall'Asta Chiara, Barbetta Laura, Baccarelli Andrea, Beck-Peccoz Paolo, Ambrosi Bruno
Institute of Endocrine Sciences, University of Milan, Ospedale Maggiore IRCCS, Milan, Italy.
Eur J Endocrinol. 2002 Oct;147(4):489-94. doi: 10.1530/eje.0.1470489.
The incidence of adrenal incidentalomas has sharply increased in recent decades and concurrent subtle endocrine abnormalities, or even subclinical conditions, have been identified. Nonetheless, data concerning possible changes in adrenal size and/or hormonal pattern during follow-up are still inadequate.
To evaluate long-term morphological and functional evolution of adrenal incidentalomas after initial diagnosis and to identify possible risk factors for hormonal hyperactivity and mass enlargement.
Sixty-four patients (34-79 years) were followed-up for 12-120 months (median 25.5 months). Initial computerized tomography scan showed a unilateral mass in 51 patients and bilateral lesions in 13 patients. Average mass diameter at diagnosis was 2.5+/-0.1 cm (range 1.0-4.0). Twelve patients had subclinical Cushing's syndrome, 41 had mild hormonal alterations, and 11 had normal adrenal function at baseline. All patients were investigated by morphological and functional evaluation 6 and 12 months after diagnosis, and then at 1-year intervals.
During follow-up, a mass size increase >/=1 cm was observed in 13 patients, and 18 developed further subtle endocrine alterations. Cumulative risk of developing endocrine abnormalities was 17% at 1 year, 29% at 2 years, and 47% at 5 years. The risk was higher in the first 2 years of follow-up if the initial tumor diameter was >or=3 cm. Overall, cumulative risk of mass enlargement was 6% at 1 year, 14% at 2 years, and 29% at 5 years, and it was greater in patients with normal adrenal function than in those with subtle hormonal abnormalities (P<0.05). One female subject showed a mass enlargement after 6 months of follow-up and was eventually diagnosed with non-Hodgkin's lymphoma.
Patients with an adrenal incidentaloma are at risk for tumor growth and development of hormonal alterations. The risk of adrenal malignancy, although not elevated, also indicates the need for long-term follow-up.
近几十年来,肾上腺偶发瘤的发病率急剧上升,同时已发现存在并发的细微内分泌异常,甚至亚临床状况。然而,关于随访期间肾上腺大小和/或激素模式可能变化的数据仍然不足。
评估肾上腺偶发瘤初诊后的长期形态和功能演变,并确定激素活性亢进和肿块增大的可能危险因素。
64例患者(年龄34 - 79岁)接受了12 - 120个月的随访(中位时间25.5个月)。初次计算机断层扫描显示,51例患者为单侧肿块,13例患者为双侧病变。诊断时肿块平均直径为2.5±0.1 cm(范围1.0 - 4.0)。12例患者有亚临床库欣综合征,41例有轻度激素改变,11例在基线时肾上腺功能正常。所有患者在诊断后6个月和12个月进行了形态和功能评估,随后每年进行一次评估。
随访期间,13例患者肿块大小增加≥1 cm,18例出现进一步细微的内分泌改变。发生内分泌异常的累积风险在1年时为17%,2年时为29%,5年时为47%。如果初始肿瘤直径≥3 cm,随访的前2年风险更高。总体而言,肿块增大的累积风险在1年时为6%,2年时为14%,5年时为29%,肾上腺功能正常的患者比有细微激素异常的患者风险更大(P<0.05)。一名女性患者在随访6个月后肿块增大,最终被诊断为非霍奇金淋巴瘤。
肾上腺偶发瘤患者有肿瘤生长和激素改变发展的风险。肾上腺恶性肿瘤的风险虽未升高,但仍表明需要长期随访。