急性自主神经病变是儿童严重动脉高血压的罕见病因

Q2 Medicine
Halszka Kamińska , Anna Kostera-Pruszczyk , Anna Potulska-Chromik , Bożena Werner
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引用次数: 1

摘要

一名7岁男孩因血压160/120 mmHg伴手、脚灼痛及心动过速而入住儿科心内科,入院后不久出现平生第一次癫痫发作。这个孩子接受了广泛的诊断过程,包括实验室检查和影像学检查,结果都不确定。急性自主神经病变最终被诊断并成功地通过静脉注射免疫球蛋白治疗。所描述的情况说明需要谨慎和开放的方法来治疗高血压患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Acute Autonomic Neuropathy as a Rare Cause of Severe Arterial Hypertension in a Child

Acute Autonomic Neuropathy as a Rare Cause of Severe Arterial Hypertension in a Child

Acute Autonomic Neuropathy as a Rare Cause of Severe Arterial Hypertension in a Child

Acute Autonomic Neuropathy as a Rare Cause of Severe Arterial Hypertension in a Child

A 7-year-old boy was admitted to the Pediatric Cardiology Department with blood pressure of 160/120 mmHg accompanied by burning pain in his hands and feet and tachycardia, followed by a seizure attack for the first time in his life, which presented shortly after admission. The child underwent a widespread diagnostic process – including laboratory tests and imaging – showing inconclusive results. Acute autonomic neuropathy was eventually diagnosed and successfully treated with intravenous immunoglobulin. The described case illustrates the need for a careful and open-minded approach to patients with hypertension.

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来源期刊
International Journal of Pediatrics and Adolescent Medicine
International Journal of Pediatrics and Adolescent Medicine Medicine-Pediatrics, Perinatology and Child Health
CiteScore
4.20
自引率
0.00%
发文量
17
审稿时长
17 weeks
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