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儿童原发性肾血管性高血压的临床谱

Clinical spectrum of intrinsic renovascular hypertension in children.

作者信息

Daniels S R, Loggie J M, McEnery P T, Towbin R B

机构信息

Department of Pediatrics, Children's Hospital Medical Center, Cincinnati, OH 45229-2899.

出版信息

Pediatrics. 1987 Nov;80(5):698-704.

PMID:2959904
Abstract

In the past two decades, 853 children and adolescents have been evaluated for elevated BP as inpatients and outpatients by the hypertension service at Children's Hospital Medical Center, Cincinnati. Most children with hypertension secondary to coarctation of the aorta and all children with glomerulonephritis are managed by other services and are not included in that total. In a retrospective study, 27 children (3%) were identified as having hypertension secondary to intrinsic renal arterial stenosis. The age at presentation ranged from 5 months to 20 years. The mean BP at that time was 171.6/114.2 mm Hg. Ten categories of causes were identified, including fibromuscular dysplasia, arteritis, Williams syndrome, neurofibromatosis, congenital malformations, blunt abdominal trauma, surgical vascular trauma-irradiation, thrombosis, congenital rubella syndrome, and unknown. Overall, symptoms were not common. However, findings of end-organ response, such as left ventricular hypertrophy and retinal vascular abnormalities were prevalent. This is not surprising given the mean BP level at presentation. Physical examination, laboratory tests, and radiologic evaluations (exclusive of renal angiography) were not useful in detecting or identifying the location and extent of the renovascular lesions. Fourteen patients were treated surgically, and 13 were managed medically. The outcome was variable for both treatment modalities. The management of renovascular hypertension in children must be individualized depending on the cause, location, and severity of the lesion, as well as the size of the child. Some forms of renovascular pathology, particularly the arteritides, may resolve spontaneously, and children with these entities should have their BP treated medically until the inflammatory process has subsided.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在过去二十年中,辛辛那提儿童医院医疗中心的高血压诊疗服务部门对853名儿童和青少年进行了住院和门诊高血压评估。大多数继发于主动脉缩窄的高血压儿童以及所有患有肾小球肾炎的儿童由其他科室诊治,未纳入该总数。在一项回顾性研究中,27名儿童(3%)被确定患有继发于肾动脉内在狭窄的高血压。发病年龄从5个月至20岁不等。当时的平均血压为171.6/114.2毫米汞柱。确定了十类病因,包括纤维肌性发育不良、动脉炎、威廉姆斯综合征、神经纤维瘤病、先天性畸形、腹部钝性创伤、手术性血管创伤 - 辐射、血栓形成、先天性风疹综合征以及不明原因。总体而言,症状并不常见。然而,诸如左心室肥厚和视网膜血管异常等靶器官反应的表现很普遍。鉴于发病时的平均血压水平,这并不奇怪。体格检查、实验室检查和影像学评估(不包括肾血管造影)在检测或确定肾血管病变的位置和范围方面并无用处。14名患者接受了手术治疗,13名接受了药物治疗。两种治疗方式的结果各不相同。儿童肾血管性高血压的治疗必须根据病因、病变位置和严重程度以及儿童的体型进行个体化。某些形式的肾血管病变,特别是动脉炎,可能会自发缓解,患有这些疾病的儿童在炎症过程消退之前应接受药物降压治疗。(摘要截选至250词)

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Clinical spectrum of intrinsic renovascular hypertension in children.儿童原发性肾血管性高血压的临床谱
Pediatrics. 1987 Nov;80(5):698-704.
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[Arterial hypertension caused by anomaly of the renal artery or its branches in children].[儿童肾动脉或其分支异常所致的动脉高血压]
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Beyond Atherosclerosis and Fibromuscular Dysplasia: Rare Causes of Renovascular Hypertension.超越动脉粥样硬化和纤维肌性发育不良:肾血管性高血压的罕见病因。
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