| 儿茶酚胺症(附12例报告) |
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| 引用本文： | 刘红耀 王东文. 儿茶酚胺症(附12例报告)[J]. 实用口腔医学杂志, 1997, 26(6): 490-492 |
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| 作者姓名： | 刘红耀 王东文 |
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| 作者单位： | 山西医科大学第一医院 |
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| 摘 要： | １２例儿茶酚胺症均经病理及手术证实,其中１０例为肾上腺嗜铬细胞瘤（ＡＭＰ）,１例肾上腺髓质增生（ＡＭＨ）,１例恶性嗜铬细胞瘤。ＣＡ和ＶＭＡ测定对诊断有特异性,ＡＭＨ的诊断依赖于病理,对于无高血压症状的嗜铬细胞瘤,认为采用“静止嗜铬细胞瘤”为妥,手术是治疗儿茶酚胺症的根本治疗方法,充分的术前准备是重要的。
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| 关 键 词： | 儿茶酚胺症 嗜铬细胞瘤 肾上腺 |
CATECHOLAMINE SYNDROME (REPORT OF 12 CASES) |
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| Abstract: | 12 cases of catecholamine syndrome were confirmed by surgery and pathology,which include 10 cases of adrenal medullary pheochromocytoma (AMP),1 case of adrenal medullary hyperplasia (AMH),and 1 case of malignant pheochromocytoma.CA and VMA assays are specific and essential for the diagnosis.The diagnosis of AMH should be confirmed by surgery and pathology.It is suggested that the term"nonfunctioning pheochromocytoma"should not be used but the term silent pheochromocytome.Surgical extirpation is the only means of cure,and meticulous preoperative preparation is essential. |
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| Keywords: | catecholamine syndrome pheochromocytoma adrenal glands |
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