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急性自主神经病变作为儿童严重动脉高血压的罕见病因

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

作者信息

Kamińska Halszka, Kostera-Pruszczyk Anna, Potulska-Chromik Anna, Werner Bożena

机构信息

Dept. of Pediatric Cardiology and General Pediatrics, Medical University of Warsaw, Poland.

Dept. of Neurology, Medical University of Warsaw, Poland.

出版信息

Int J Pediatr Adolesc Med. 2021 Jun;8(2):121-124. doi: 10.1016/j.ijpam.2020.06.006. Epub 2020 Jul 8.

DOI:10.1016/j.ijpam.2020.06.006
PMID:34084885
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8144862/
Abstract

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.

摘要

一名7岁男孩因血压160/120 mmHg入院至儿科心脏病科,伴有手脚灼痛和心动过速,入院后不久首次出现癫痫发作。该患儿接受了广泛的诊断过程——包括实验室检查和影像学检查——结果均无定论。最终诊断为急性自主神经病变,并通过静脉注射免疫球蛋白成功治愈。所述病例表明,对于高血压患者需要采取谨慎且开放的态度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e1/8144862/af10b89d3bd9/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e1/8144862/a36c6ba0db9a/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e1/8144862/63f44def35b6/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e1/8144862/af10b89d3bd9/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e1/8144862/a36c6ba0db9a/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e1/8144862/63f44def35b6/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e1/8144862/af10b89d3bd9/gr3.jpg

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