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Primary erythromelalgia mainly manifested by hypertensive crisis: A case report and literature review

BACKGROUND: Primary erythrocytic (PEM) is a rare autosomal dominant single gene disease. Most of the changes of gene loci can be found by whole exon gene sequencing, and the clinical symptoms and patient survival can be improved by specific site-to-site drug treatment. The other manifestations of th...

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Autores principales: Feng, Shuo, He, Zhanwen, Que, Liping, Luo, Xiangyang, Liang, Liyang, Li, Dongfang, Qin, Lijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424545/
https://www.ncbi.nlm.nih.gov/pubmed/36052366
http://dx.doi.org/10.3389/fped.2022.796149
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author Feng, Shuo
He, Zhanwen
Que, Liping
Luo, Xiangyang
Liang, Liyang
Li, Dongfang
Qin, Lijun
author_facet Feng, Shuo
He, Zhanwen
Que, Liping
Luo, Xiangyang
Liang, Liyang
Li, Dongfang
Qin, Lijun
author_sort Feng, Shuo
collection PubMed
description BACKGROUND: Primary erythrocytic (PEM) is a rare autosomal dominant single gene disease. Most of the changes of gene loci can be found by whole exon gene sequencing, and the clinical symptoms and patient survival can be improved by specific site-to-site drug treatment. The other manifestations of this patient population are not remarkable. After the application of common drugs, the toxicity and side effects can be limiting. In addition to other common clinical manifestations, we found that the only unique manifestation of this patient was hypertensive crisis. Following multidisciplinary diagnosis and treatment (MDT), we decided to first control hypertension to alleviate the acute and critical patients. However, after controlling the hypertensive crisis, we unexpectedly found that the clinical symptoms of the patients had been significantly improved. Therefore, we concluded that the use of antihypertensive drugs can treat erythematous limb pain with the clinical manifestation of hypertensive crisis. Here, we describe a typical PEM disease, primary clinical features, diagnosis and treatment. METHODS: Medical records of an 8-year-old boy with PEM were analyzed retrospectively, which included clinical characteristics, follow-up information, and SCN9A (Sodium Voltage-Gated Channel Alpha Subunit 9) gene analysis. RESULTS: The 8-year-old boy had complained of abnormal paresthesia in his feet and ankles with burning sensation and pain for 2 years. The skin of both lower legs was red and underwent ichthyosis and lichenification. Genetic analysis confirmed the existence of a SCN9A gene mutation. The symptoms were gradually improved by treating with intravenous drip and oral administration of nitroglycerin to slow his heart rhythm. CONCLUSION: Primary erythrocytic is characterized by skin ulceration, redness, elevated temperature, and severe burning pain primarily in both lower extremities. PEM can be diagnosed by genetic analysis. As this case demonstrates, treating with nitroglycerin as the drug of choice to control the hypertensive crisis significantly improved the symptoms of PEM and hypertension in this patient.
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spelling pubmed-94245452022-08-31 Primary erythromelalgia mainly manifested by hypertensive crisis: A case report and literature review Feng, Shuo He, Zhanwen Que, Liping Luo, Xiangyang Liang, Liyang Li, Dongfang Qin, Lijun Front Pediatr Pediatrics BACKGROUND: Primary erythrocytic (PEM) is a rare autosomal dominant single gene disease. Most of the changes of gene loci can be found by whole exon gene sequencing, and the clinical symptoms and patient survival can be improved by specific site-to-site drug treatment. The other manifestations of this patient population are not remarkable. After the application of common drugs, the toxicity and side effects can be limiting. In addition to other common clinical manifestations, we found that the only unique manifestation of this patient was hypertensive crisis. Following multidisciplinary diagnosis and treatment (MDT), we decided to first control hypertension to alleviate the acute and critical patients. However, after controlling the hypertensive crisis, we unexpectedly found that the clinical symptoms of the patients had been significantly improved. Therefore, we concluded that the use of antihypertensive drugs can treat erythematous limb pain with the clinical manifestation of hypertensive crisis. Here, we describe a typical PEM disease, primary clinical features, diagnosis and treatment. METHODS: Medical records of an 8-year-old boy with PEM were analyzed retrospectively, which included clinical characteristics, follow-up information, and SCN9A (Sodium Voltage-Gated Channel Alpha Subunit 9) gene analysis. RESULTS: The 8-year-old boy had complained of abnormal paresthesia in his feet and ankles with burning sensation and pain for 2 years. The skin of both lower legs was red and underwent ichthyosis and lichenification. Genetic analysis confirmed the existence of a SCN9A gene mutation. The symptoms were gradually improved by treating with intravenous drip and oral administration of nitroglycerin to slow his heart rhythm. CONCLUSION: Primary erythrocytic is characterized by skin ulceration, redness, elevated temperature, and severe burning pain primarily in both lower extremities. PEM can be diagnosed by genetic analysis. As this case demonstrates, treating with nitroglycerin as the drug of choice to control the hypertensive crisis significantly improved the symptoms of PEM and hypertension in this patient. Frontiers Media S.A. 2022-08-16 /pmc/articles/PMC9424545/ /pubmed/36052366 http://dx.doi.org/10.3389/fped.2022.796149 Text en Copyright © 2022 Feng, He, Que, Luo, Liang, Li and Qin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Feng, Shuo
He, Zhanwen
Que, Liping
Luo, Xiangyang
Liang, Liyang
Li, Dongfang
Qin, Lijun
Primary erythromelalgia mainly manifested by hypertensive crisis: A case report and literature review
title Primary erythromelalgia mainly manifested by hypertensive crisis: A case report and literature review
title_full Primary erythromelalgia mainly manifested by hypertensive crisis: A case report and literature review
title_fullStr Primary erythromelalgia mainly manifested by hypertensive crisis: A case report and literature review
title_full_unstemmed Primary erythromelalgia mainly manifested by hypertensive crisis: A case report and literature review
title_short Primary erythromelalgia mainly manifested by hypertensive crisis: A case report and literature review
title_sort primary erythromelalgia mainly manifested by hypertensive crisis: a case report and literature review
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424545/
https://www.ncbi.nlm.nih.gov/pubmed/36052366
http://dx.doi.org/10.3389/fped.2022.796149
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