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作 者:刘定益[1] 郑崇达[1] 陈其智[1] 张祖豹[1] 吴瑜璇[1] 王瑞伦[1] 凌建煜
机构地区:[1]第二医科大学瑞金医院泌尿外科
出 处:《中华外科杂志》1998年第5期295-296,共2页Chinese Journal of Surgery
摘 要:目的提高对嗜铬细胞瘤合并肾动脉狭窄(RAS)的诊断与治疗水平。方法报告4例嗜铬细胞瘤合并RAS。4例患者均行嗜铬细胞瘤切除术。结果2例切除RAS肾及1例松解局部粘连所致RAS患者血压均正常,而1例松解长段RAS后保留RAS肾者持续高血压。结论当嗜铬细胞瘤定性与定位之后在上腹部或背部闻及血管杂音,一侧肾影变小或遇到单用α受体阻滞剂降血压效果欠佳,需加用血管紧张素转化酶抑制剂者,以及嗜铬细胞瘤术后血压持续不降而又排除残留嗜铬细胞瘤者均应考虑合并RAS可能。对因嗜铬细胞瘤直接压迫,粘连造成肾动脉成角或局部狭窄者,在去除嗜铬细胞瘤及松解粘连之后RAS多能缓解,而对嗜铬细胞瘤致肾动脉广泛狭窄或闭塞,肾实质明显萎缩者,应切除患肾。Objective To improve the diagnosis of coexisting pheochromocytoma and renal artery stenosis.Method Four patients with coexisting pheochromocytoma and renal arterystenosis were treated.Result After removal of the pheochromocytoma,the blood pressure became normal in two patients combined with resection of kidney with renal artery stenosis,and one patient with local adhesion loosened.The hypertension, however,persisted in another patient after the resection of pheochromocytoma even though the long segment of renal artery stenosis was relieved.Conclusion After pheochromocytoma was diagnosed with its known position, coexisting renal artery stenosis should be suspected accerding to one of the following conditions:(1) Vascular murmurs are noted at the area of the upper abdomen or back;(2)One of the kidneys becomes less sized;(3)Using the inhibitor of receptor α only has no effect lowering blood pressure and it is necessary to add the inhibitor of angiotension; (4)Postoperative hypertension does not resolve when no remaining pheochromocytoma is present.the renal artery stenosis can be reversed after both removal of pheochromocytoma and loosening of adhesion in case of stenosis due to the pressure of the tumor and adhesion caused renal artery angling and local stricture.Extensive stenosis or closure,however,can not becorrected with severe atrophy of renal parenchyma due to pheochromocytoma, and the resection of kidney should be indicated.
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