论文部分内容阅读
嗜铬细胞瘤是一种少见病,约占高血压病人总数的0.5%(0.07～2%)。过去一直认为本病是一种凶险的功能性肿瘤,近年来由于对本病的警惕性提高,加之临床生化及影象学诊断技术的进步,病例报告逐年增多。本文报告我院自1985年以来收治的3例以及笔者在外院所遇到的4例(2例术前确诊,2例以腹部包块手术探查),复习近期文献,对诊断和治疗谈点体会。临床资料一、一般资料:男4例,女3例。19至65岁,平均46岁。二、肿瘤部位及病理性质:右肾上腺4例,胸主动脉旁1例,小肠系膜根部1例,右肾上腺并结肠肝区1例。良性6例,1例恶性侵犯结肠壁平
Pheochromocytoma is a rare disease that accounts for about 0.5% (0.07 to 2%) of the total number of hypertensive patients. In the past, this disease was considered to be a dangerous functional tumor. In recent years, due to the increased vigilance of the disease, combined with advances in clinical biochemistry and video diagnostic techniques, case reports have been increasing year by year. This article reports 3 cases admitted in our hospital since 1985 and 4 cases encountered by the author in the external hospital (2 cases confirmed before surgery, 2 cases were examined with abdominal masses), reviewed recent literature, and talked about diagnosis and treatment. . Clinical data I. General information: 4 males and 3 females. 19 to 65 years old, an average of 46 years old. Second, the tumor site and pathological nature: 4 cases of right adrenal gland, 1 case of thoracic aorta, 1 case of small mesenteric root, 1 case of right adrenal and colonic liver area. Benign 6 cases, 1 case of malignant invasion of the colon wall