Tisnado J, Amendola M A, Konerding K F, Shirazi K K, Beachley M C
J Comput Assist Tomogr. 1980 Dec;4(6):853-9. doi: 10.1097/00004728-198012000-00021.
We report eight patients studied by computed tomography (CT) and arteriography and one patient studied by CT only and compare the value of both methods in the preoperative localization of pheochromocytoma. Single adrenal tumors were found in six adults (four were right sided and two were left sided). A 15-year-old child had bilateral adrenal tumors, and a 12-year-old child had a left adrenal tumor. An extraadrenal pheochromocytoma was found in another adult patient. Computed tomography demonstrated all but one tumor (a right adrenal lesion measuring 2.5 cm in the child with bilateral pheochromocytomas, both well shown by angiography). Arteriography, including subtraction films, demonstrated all but one tumor (an avascular extraadrenal pheochromocytoma measuring 4 x 8 cm well shown by CT). We believe that both CT and angiography contribute significant information in the preoperative evaluation of patients suspected of harboring a pheochromocytoma.
我们报告了8例接受计算机断层扫描(CT)和动脉造影检查的患者以及1例仅接受CT检查的患者,并比较了这两种方法在嗜铬细胞瘤术前定位中的价值。6名成年人发现了单侧肾上腺肿瘤(4例在右侧,2例在左侧)。一名15岁儿童患有双侧肾上腺肿瘤,一名12岁儿童患有左侧肾上腺肿瘤。另一名成年患者发现了肾上腺外嗜铬细胞瘤。CT显示了除1个肿瘤外的所有肿瘤(在患有双侧嗜铬细胞瘤的儿童中,一个2.5厘米的右侧肾上腺病变,血管造影很好地显示了这两个肿瘤)。动脉造影,包括减影片,显示了除1个肿瘤外的所有肿瘤(一个4×8厘米的无血管肾上腺外嗜铬细胞瘤,CT很好地显示了该肿瘤)。我们认为,CT和血管造影在疑似患有嗜铬细胞瘤患者的术前评估中都提供了重要信息。