Zhang S Z
Lanzhou General Hospital of Lanzhou Unit of People's Liberation Army.
Zhonghua Wai Ke Za Zhi. 1990 Nov;28(11):679-81, 703.
From 1958 to 1990, 49 patients with pheochromocytoma were treated surgically. The tumors were located in the adrenal gland in 34 cases (69.4%) and in the extra-adrenal gland in 15 cases (30.6%). In two cases the tumors were pheochromoblastoma and in 6 cases the tumors were asymptomatic. Determination of urine VMA has a screening value for patients with pheochromocytoma. The corresponding rate was 91.3% by B-ultrasonography to localize the tumor. CT scanning can clearly identify pheochromocytoma of its size and relation to the adjacent organs, which may provide a basis for the selection of operative methods. Administration of alpha-adrenoceptor blocking drugs and expanding blood volume are very important procedures, which can effectively reduce the mortality rate.
1958年至1990年,49例嗜铬细胞瘤患者接受了手术治疗。肿瘤位于肾上腺者34例(69.4%),位于肾上腺外者15例(30.6%)。2例为嗜铬母细胞瘤,6例为无症状肿瘤。尿香草扁桃酸(VMA)测定对嗜铬细胞瘤患者有筛查价值。B超定位肿瘤的符合率为91.3%。CT扫描能清晰显示嗜铬细胞瘤的大小及其与邻近器官的关系,可为手术方式的选择提供依据。应用α肾上腺素能受体阻断药及扩容是非常重要的措施,可有效降低死亡率。