Lee James A, Zarnegar Rasa, Shen Wen T, Kebebew Electron, Clark Orlo H, Duh Quan-Yang
Division of Gastrointestinal/Endocrine Surgery, Columbia University Medical Center, New York, New York, USA.
Arch Surg. 2007 Sep;142(9):870-3; discussion 73-4. doi: 10.1001/archsurg.142.9.870.
To assess the risk of pheochromocytoma in patients with borderline-elevated urine or plasma metanephrine levels.
Retrospective review.
University tertiary care center.
Forty-two consecutive patients with adrenal incidentalomas (defined as adrenal tumors identified during routine imaging for another condition) who were treated at the UCSF (University of California, San Francisco) Medical Center between January 1, 1995, and July 31, 2005. Patients with genetic syndromes were excluded.
Laparoscopic adrenalectomy for adrenal incidentaloma based on size criteria and preoperative hormonal test results.
Urine or plasma metanephrine and catecholamine levels, tumor size, and presence of pheochromocytoma.
Of 42 patients, 14 (33%) had a pheochromocytoma (11 of whom had clear-cut elevations in urine or plasma metanephrine levels defined as greater than 2 times the upper limit of normal) and 28 did not. Ten of the 42 patients (24%) had borderline elevations in urine or plasma metanephrine levels (defined as 1-2 times the upper limit of normal), 3 of whom had a pheochromocytoma (30%). Of patients with borderline elevations, mean +/- SD tumor size was 5.4 +/- 3.1 and 4.8 +/- 1.9 cm for patients with and without pheochromocytoma, respectively (P = .37). In these 10 patients, no clinical factors (age, sex, hypertension, presence of symptoms, number of antihypertensive medications, preoperative hemodynamics, or size of tumor on computed tomographic scan) allowed differentiation between those with and without pheochromocytoma.
Thirty percent of patients with adrenal incidentaloma and borderline-elevated urine or plasma metanephrine levels had a pheochromocytoma. Clinical factors cannot distinguish between those with and without pheochromocytoma. In this group of patients, we advocate either routine alpha-blockade preoperatively or further diagnostic tests to better characterize the tumor.
评估尿或血浆间甲肾上腺素水平临界升高的患者患嗜铬细胞瘤的风险。
回顾性研究。
大学三级医疗中心。
1995年1月1日至2005年7月31日期间在加州大学旧金山分校医学中心接受治疗的42例肾上腺偶发瘤患者(定义为在因其他疾病进行常规影像学检查时发现的肾上腺肿瘤)。排除患有遗传综合征的患者。
根据大小标准和术前激素检测结果,对肾上腺偶发瘤进行腹腔镜肾上腺切除术。
尿或血浆间甲肾上腺素和儿茶酚胺水平、肿瘤大小以及嗜铬细胞瘤的存在情况。
42例患者中,14例(33%)患有嗜铬细胞瘤(其中11例尿或血浆间甲肾上腺素水平明显升高,定义为高于正常上限的2倍),28例未患。42例患者中有10例(24%)尿或血浆间甲肾上腺素水平临界升高(定义为正常上限的1 - 2倍),其中3例患有嗜铬细胞瘤(30%)。在临界升高的患者中,患有和未患嗜铬细胞瘤的患者平均肿瘤大小分别为5.4±3.1 cm和4.8±1.9 cm(P = 0.37)。在这10例患者中,没有临床因素(年龄、性别、高血压、症状的存在、抗高血压药物的数量、术前血流动力学或计算机断层扫描上的肿瘤大小)能够区分患有和未患嗜铬细胞瘤的患者。
肾上腺偶发瘤且尿或血浆间甲肾上腺素水平临界升高的患者中有30%患有嗜铬细胞瘤。临床因素无法区分患有和未患嗜铬细胞瘤的患者。在这组患者中,我们主张术前常规使用α受体阻滞剂或进一步进行诊断性检查以更好地明确肿瘤特征。