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[嗜铬细胞瘤的诊断与治疗。49例报告]

[Diagnosis and treatment of pheochromocytoma. Report of 49 cases].

作者信息

Zhang S Z

机构信息

Lanzhou General Hospital of Lanzhou Unit of People's Liberation Army.

出版信息

Zhonghua Wai Ke Za Zhi. 1990 Nov;28(11):679-81, 703.

PMID:1982256
Abstract

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.

摘要

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。

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