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儿茶酚胺症(附86例报告) 被引量:16

Catecholamine syndrome (report of 86 cases)
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摘要 报告86例儿茶酚胺症。其中肾上腺嗜铬细胞瘤74例(86%),肾上腺外嗜铬细胞瘤10例(11.6%),肾上腺髓质增生(AMH)2例(2.3%)。CA及VMA测定对诊断有特异性,B超及CT对肾上腺嗜铬细胞瘤的诊断率分别为93%和95%。肾上腺外嗜铬细胞瘤有多发性、复发性,恶性率明显增高,无症状嗜铬细胞瘤占8.1%。对无功能肾上腺肿瘤及源于腹膜后的上腹部肿物,要注意嗜铬细胞瘤的可能。AMH最可靠的诊断是术中所见及病理改变,手术是根本治疗方法,充分的术前准备是重要的。 cases of catecholamine syndrome were confirmed by surgery and pathology.74 cases(86%)are adrenal pheochromocytoma,10(11.6%)being extradrenal pheochromocytoma and 2(2.3%)adrenal medullary hyperplasia(AMH).CA and VMA assay are specific and essential for the diagnosis.The accurate rate of localization and diagnosis with B-US and CT is 93%,and 95% for adrenal pheochromocytoma.The extraadrenal pheochromocytoma was often multiple.recurrent with a high tendency to malignancy.There is only 7 cases(8.l%)of asymptomatic pheochromiocytoma.The preoperative preparation of the asymptomatic adrenal pheochromocytoma or upper retroperitoneal pheochromocytoma should be the same as adrenal ones.The diagnosis of AMH should be confirmed by surgery and pathology.Surgical extirpationis the only means of cure and meticulous preoperativepreparation is essential.
出处 《中华泌尿外科杂志》 CAS CSCD 北大核心 1995年第2期89-91,共3页 Chinese Journal of Urology
关键词 儿茶酚胺 肾上腺 嗜铬细胞瘤 儿茶酚胺症 Catecholamine Adrenal glandspheochromocytoma
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参考文献3

  • 1张祖豹,中华泌尿外科杂志,1993年,14卷,141页
  • 2吴阶平,中华泌尿外科杂志,1985年,6卷,1页
  • 3吴阶平,中华医学杂志,1977年,57卷,331页

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