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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 wide...

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Autores principales: Kamińska, Halszka, Kostera-Pruszczyk, Anna, Potulska-Chromik, Anna, Werner, Bożena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: King Faisal Specialist Hospital and Research Centre 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144862/
https://www.ncbi.nlm.nih.gov/pubmed/34084885
http://dx.doi.org/10.1016/j.ijpam.2020.06.006
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author Kamińska, Halszka
Kostera-Pruszczyk, Anna
Potulska-Chromik, Anna
Werner, Bożena
author_facet Kamińska, Halszka
Kostera-Pruszczyk, Anna
Potulska-Chromik, Anna
Werner, Bożena
author_sort Kamińska, Halszka
collection PubMed
description 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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spelling pubmed-81448622021-06-02 Acute Autonomic Neuropathy as a Rare Cause of Severe Arterial Hypertension in a Child Kamińska, Halszka Kostera-Pruszczyk, Anna Potulska-Chromik, Anna Werner, Bożena Int J Pediatr Adolesc Med Original Article 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. King Faisal Specialist Hospital and Research Centre 2021-06 2020-07-08 /pmc/articles/PMC8144862/ /pubmed/34084885 http://dx.doi.org/10.1016/j.ijpam.2020.06.006 Text en © 2020 Publishing services provided by Elsevier B.V. on behalf of King Faisal Specialist Hospital & Research Centre (General Organization), Saudi Arabia. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Kamińska, Halszka
Kostera-Pruszczyk, Anna
Potulska-Chromik, Anna
Werner, Bożena
Acute Autonomic Neuropathy as a Rare Cause of Severe Arterial Hypertension in a Child
title Acute Autonomic Neuropathy as a Rare Cause of Severe Arterial Hypertension in a Child
title_full Acute Autonomic Neuropathy as a Rare Cause of Severe Arterial Hypertension in a Child
title_fullStr Acute Autonomic Neuropathy as a Rare Cause of Severe Arterial Hypertension in a Child
title_full_unstemmed Acute Autonomic Neuropathy as a Rare Cause of Severe Arterial Hypertension in a Child
title_short Acute Autonomic Neuropathy as a Rare Cause of Severe Arterial Hypertension in a Child
title_sort acute autonomic neuropathy as a rare cause of severe arterial hypertension in a child
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144862/
https://www.ncbi.nlm.nih.gov/pubmed/34084885
http://dx.doi.org/10.1016/j.ijpam.2020.06.006
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