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嗜铬细胞瘤通过CT扫描并结合临床和生化检查,绝大多数均能明确肿瘤的定位和定性诊断。手术切除肿瘤是本病唯一的根治方法。我们对行CT扫描并经手术和病理证实的14例分析如下: 资料与方法一、本组病例均采用GE8800型扫描机进行检查,层厚和层距均为5mm。对两例增强患者均一次性静脉内推注60％泛影葡胺60ml。二、本组男3例,女11例,女性为男性的3.7倍,明显高于其它文献的报道;年龄15至65岁,平均为35.3岁,15至40岁占50％,45岁以下占86％。三、CT表现:14例共15个肿瘤,1例为双侧肾上腺嗜铬细胞瘤。11例肿瘤位于肾上腺,
Pheochromocytoma by CT scan combined with clinical and biochemical tests, the vast majority can identify the location and qualitative diagnosis of the tumor. Surgical removal of the tumor is the only cure for the disease. Our analysis of 14 cases of CT scan and confirmed by surgery and pathology is as follows: Materials and Methods First, this group of patients were examined using a GE8800 scanner, and the thickness and layer distance were 5mm. For both patients, one-time intravenous infusion of 60% diatrizoate 60 ml was performed. 2. There are 3 males and 11 females in this group, 3.7 times as much as females, which is significantly higher than other reports; ages 15 to 65, with an average of 35.3 years, 15 to 40 years, 50%, accounting for less than 45 years of age. 86%. Three, CT manifestations: 14 cases of a total of 15 tumors, 1 case of bilateral adrenal pheochromocytoma. Eleven tumors were located in the adrenal gland