摘要
本文报告组织学确诊的嗜铬细胞瘤23例。其中男8例,女15例;平均年龄40岁;位于肾上腺内11例,腹膜后4例,腹主动脉旁3例,左右肾门各1例,膀胱壁2例,胸主动脉旁1例;良性21例,恶性2例。术前尿 VMA 半定量 R 值测定阳性率为65.2%(15/23),Regitine 试验阳性率75.0%(9/12),B 超和 CT 定位准确率为83.3%(10/12)和89.5%(8/9)。本文结合近年文献,对嗜铬细胞瘤组织病理、临床表现、生化检测、定位诊断与内科治疗作了较全面复习。
A retrospective analysis of 23 patients with pheochromoeytoma was presented.Of them,8 were male and 15 female.The mean age was 40 years,with a range of14 to 64.Eleven cases were in the intraadrenal,4 retro-peritoneal,3 near the abdo-minal aorta,2 in the bladder wall,one at the left and another at the right renalhilum and the last one in the chest.Of the 23 cases,21 were benign,2 malignant.The positive rate of urine VMA was 65.2%(15/23),Regitine test 75.0%(9/12),CT89.5%(8/9)and B-Ultrasound 83.3%(10/12).The patho-histology,clinical manifes-tations,laboratory measurements,localization and medical treatment of pheochromo-cytoma were discussed with review of literature.
出处
《天津医药》
CAS
1991年第8期455-458,共4页
Tianjin Medical Journal
关键词
嗜铬细胞瘤
诊断
病理
pheochromocytoma
clinic
pathology
diagnosis
