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嗜铬细胞瘤与慢性血液透析的诊断考量:病例报告及文献综述

Diagnostic considerations in pheochromocytoma and chronic hemodialysis: case report and review of the literature.

作者信息

Stumvoll M, Radjaipour M, Seif F

机构信息

University of Rochester Medical School, Division of Endocrinology and Metabolism, NY 14642, USA.

出版信息

Am J Nephrol. 1995;15(2):147-51. doi: 10.1159/000168820.

Abstract

We present a patient on long-term hemodialysis (LTH) discovered to have a pheochromocytoma. A thorough workup pertaining his catecholamine status was performed, and intraoperative catecholamine changes were monitored. This condition poses some analytical difficulties as both interpretation of plasma catecholamine measurements and determination of their metabolic products are impaired. The literature about catecholamines with respect to hemodialysis is reviewed, and the known cases of pheochromocytoma in LTH patients are discussed. Predialysis norepinephrine concentrations were almost consistently elevated though less than 3-fold when compared to normal controls. Epinephrine is not significantly different in both groups. At least a 3.3-fold increase of epinephrine or norepinephrine in LTH patients with adrenal pheochromocytomas is observed. We conclude that plasma epinephrine elevations can be evaluated in the conventional manner, and norepinephrine concentrations beyond a 3-fold elevation should raise the suspicion of a pathological catechol excess syndrome. The interpretation of plasma homovanillic acid and vanillylmandelic acid in this condition is complicated by the lack of data in LTH patients without pheochromocytoma. Markedly elevated baseline concentrations for these parameters are assumed.

摘要

我们报告一例长期血液透析(LTH)患者,该患者被发现患有嗜铬细胞瘤。针对其儿茶酚胺状态进行了全面检查,并监测了术中儿茶酚胺的变化。这种情况带来了一些分析上的困难,因为血浆儿茶酚胺测量值的解读及其代谢产物的测定均受到影响。本文回顾了关于血液透析与儿茶酚胺的文献,并讨论了LTH患者中已知的嗜铬细胞瘤病例。透析前去甲肾上腺素浓度几乎持续升高,不过与正常对照组相比升高幅度小于3倍。两组间肾上腺素无显著差异。观察到LTH合并肾上腺嗜铬细胞瘤患者的肾上腺素或去甲肾上腺素至少升高3.3倍。我们得出结论,血浆肾上腺素升高可按常规方式评估,而去甲肾上腺素浓度升高超过3倍应引起对病理性儿茶酚胺过量综合征的怀疑。由于缺乏无嗜铬细胞瘤的LTH患者的数据,在此情况下血浆高香草酸和香草扁桃酸的解读较为复杂。假定这些参数的基线浓度显著升高。

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