Corsello S M, Della Casa S, Bollanti L, Rufini V, Rota C A, Danza F, Colasanti S, Vellante C, Troncone L, Barbarino A
Institute of Endocrinology, Catholic University School of Medicine, Rome, Italy.
Exp Clin Endocrinol. 1993;101(3):131-7. doi: 10.1055/s-0029-1211219.
In the last two years we have examined 17 consecutive patients (11 females and 6 males, 20-66 years old) in whom an unsuspected adrenal mass was discovered by ultrasonography or computed tomography performed for unrelated reasons. Pathological diagnosis was available in 11 cases based on surgical excision in 9 (2 pheochromocytomas of 5 and 12 cm in diameter; 2 ganglioneuromas of 5 and 6 cm; and 5 benign cortical adenomas between 3 and 5 cm), autopsy in 1 (a disseminated malignant pheochromocytoma of 16 cm) and fine-needle biopsy in 1 (a pseudo-adrenal mass of 6 cm, that was a regenerative hepatic nodule). The remaining 6 non histologically diagnosed masses were less than 3 cm in diameter. Endocrine studies showed elevated urinary excretion of catecholamines, vanillylmandelic acid and metanephrines in the pheochromocytomas and borderline high values in ganglioneuromas. A low plasma renin activity was encountered in 2 operated cortical adenomas and 3 non operated incidentalomas. In 2 of the latters aldosterone serum levels were elevated and the final diagnoses respectively were Conn's adenoma and dexamethasone-suppressible hyperaldosteronism with bilateral nodular hyperplasia. An inappropriate cortisol secretion was documented in a cortical adenoma removed. Radio-cholesterol scintiscan showed unilateral or increased uptake on the side of adrenal mass (concordant uptake) in the 5 benign cortical adenomas removed and in 4 non operated incidentalomas. A decreased uptake on the side of the adrenal mass (discordant uptake) was found in the 2 ganglioneuromas while an indeterminate bilateral uptake was found in the 2 remaining non operated incidentalomas and in the pseudo-adrenal mass.(ABSTRACT TRUNCATED AT 250 WORDS)
在过去两年中,我们对17例连续患者(11名女性和6名男性,年龄20 - 66岁)进行了检查,这些患者因无关原因接受超声检查或计算机断层扫描时意外发现肾上腺肿块。11例患者有病理诊断结果,其中9例通过手术切除(2例直径分别为5厘米和12厘米的嗜铬细胞瘤;2例直径分别为5厘米和6厘米的神经节神经瘤;5例直径在3至5厘米之间的良性皮质腺瘤),1例通过尸检(1例直径16厘米的播散性恶性嗜铬细胞瘤),1例通过细针活检(1例直径6厘米的假肾上腺肿块,为再生性肝结节)。其余6例未进行组织学诊断的肿块直径小于3厘米。内分泌研究显示,嗜铬细胞瘤患者尿中儿茶酚胺、香草扁桃酸和甲氧基肾上腺素排泄量升高,神经节神经瘤患者的值略高。2例接受手术的皮质腺瘤和3例未手术的偶发瘤患者血浆肾素活性较低。后3例中有2例醛固酮血清水平升高,最终诊断分别为Conn腺瘤和双侧结节性增生的地塞米松可抑制性醛固酮增多症。1例切除的皮质腺瘤存在皮质醇分泌异常。放射性胆固醇闪烁扫描显示,5例切除的良性皮质腺瘤和4例未手术的偶发瘤中,肾上腺肿块侧有单侧或摄取增加(摄取一致)。2例神经节神经瘤中肾上腺肿块侧摄取减少(摄取不一致),其余2例未手术的偶发瘤和假肾上腺肿块中双侧摄取情况不确定。(摘要截选至250字)