有胶质母细胞瘤和脑水肿病史的难治性继发性高血压1例

IF 0.4 Q4 PERIPHERAL VASCULAR DISEASE
Małgorzata Placek, M. Sołtysiak, J. Drozdowski, J. Wolf
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引用次数: 0

摘要

我们报告了一位患者的病史,他患有难以控制的高血压,中枢神经系统肿块和几种合并症,这些合并症使降压药特别具有挑战性。患者被诊断为胶质母细胞瘤,肾血管狭窄至单肾,脑水肿由脑组织肿块和全身血压过高引起。在本病例中,我们面临指南推荐的RAAS阻滞剂、β -阻滞剂和几种利尿剂治疗的几个禁忌症,这些禁忌症由以下因素决定:(1)唯一剩余的肾脏肾动脉狭窄,(2)肌酐清除率降低,(3)继发于脑水肿的反射性心动过缓。基于证据的建议并不能阐明与突发高血压相关的所有临床方面,因为证据很少;因此,我们觉得分享我们的经验很有趣。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Difficult-to-control secondary hypertension in a patient with history of glioblastoma, and cerebral edema — a case study
We report a history of a patient with difficult-to-control high blood pressure, central nervous system mass and several comorbidities which altogether made the blood-lowering medication particularly challenging. Patient was diagnosed with glioblastoma, renovascular stenosis to a single kidney, and cerebral edema resulting from both cerebral tissue mass and exceedingly high systemic blood pressure. In the presented case we faced several contraindications to the guideline-recommended treatment with RAAS blockers, beta-blockers, and several diuretic classes which were determined by (1) the only remaining kidney’s renal artery stenosis, (2) decreased creatinine clearance and (3) reflex bradycardia secondary to cerebral edema. Evidence-based recommendations do not clarify all clinical aspects related to emergent high blood pressure because the evidence is sparse; therefore, we found it interesting to share our experience.
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来源期刊
Arterial Hypertension
Arterial Hypertension PERIPHERAL VASCULAR DISEASE-
CiteScore
0.70
自引率
14.30%
发文量
19
审稿时长
10 weeks
期刊介绍: Arterial Hypertension hereinafter referred to as ‘AH’ or ′the Journal′, is a peer-reviewed, open access journal covering broad spectrum of topics in hypertension and aiming to advance the knowledge and science of this constantly evolving field. The Journal is the official quarterly of the Polish Society of Hypertension and publishes review articles, original clinical and experimental investigations in the field of arterial hypertension, case reports, letters and editorial comments. The Journal''s content has been published predominantly in full text English since 2015.
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