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Erythromelalgia in an Adolescent Female
Erythromelalgia is a disabling syndrome of paroxysmal vasodilation affecting the feet, hands and face characterised by patient’s cooling behaviour to achieve symptom relief. It can be primary or secondary and although a rare disorder it has been described in children and adolescents. We describe the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Mediterranean Journal of Rheumatology (MJR)
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450199/ https://www.ncbi.nlm.nih.gov/pubmed/36128208 http://dx.doi.org/10.31138/mjr.33.2.256 |
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author | Mamatsi, Eleftheria Giorgi, Melpomeni Dinopoulos, Argirios Papaevangelou, Vasiliki Fotis, Lampros |
author_facet | Mamatsi, Eleftheria Giorgi, Melpomeni Dinopoulos, Argirios Papaevangelou, Vasiliki Fotis, Lampros |
author_sort | Mamatsi, Eleftheria |
collection | PubMed |
description | Erythromelalgia is a disabling syndrome of paroxysmal vasodilation affecting the feet, hands and face characterised by patient’s cooling behaviour to achieve symptom relief. It can be primary or secondary and although a rare disorder it has been described in children and adolescents. We describe the case of a 14-year-old female diagnosed with primary erythromelalgia successfully treated with aspirin, amitriptyline, and carbamazepine. |
format | Online Article Text |
id | pubmed-9450199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Mediterranean Journal of Rheumatology (MJR) |
record_format | MEDLINE/PubMed |
spelling | pubmed-94501992022-09-19 Erythromelalgia in an Adolescent Female Mamatsi, Eleftheria Giorgi, Melpomeni Dinopoulos, Argirios Papaevangelou, Vasiliki Fotis, Lampros Mediterr J Rheumatol Case Report Erythromelalgia is a disabling syndrome of paroxysmal vasodilation affecting the feet, hands and face characterised by patient’s cooling behaviour to achieve symptom relief. It can be primary or secondary and although a rare disorder it has been described in children and adolescents. We describe the case of a 14-year-old female diagnosed with primary erythromelalgia successfully treated with aspirin, amitriptyline, and carbamazepine. The Mediterranean Journal of Rheumatology (MJR) 2022-06-30 /pmc/articles/PMC9450199/ /pubmed/36128208 http://dx.doi.org/10.31138/mjr.33.2.256 Text en © 2022 The Mediterranean Journal of Rheumatology (MJR) https://creativecommons.org/licenses/by/4.0/This work is licensed under and Creative Commons Attribution-NonCommercial 4.0 International License. |
spellingShingle | Case Report Mamatsi, Eleftheria Giorgi, Melpomeni Dinopoulos, Argirios Papaevangelou, Vasiliki Fotis, Lampros Erythromelalgia in an Adolescent Female |
title | Erythromelalgia in an Adolescent Female |
title_full | Erythromelalgia in an Adolescent Female |
title_fullStr | Erythromelalgia in an Adolescent Female |
title_full_unstemmed | Erythromelalgia in an Adolescent Female |
title_short | Erythromelalgia in an Adolescent Female |
title_sort | erythromelalgia in an adolescent female |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450199/ https://www.ncbi.nlm.nih.gov/pubmed/36128208 http://dx.doi.org/10.31138/mjr.33.2.256 |
work_keys_str_mv | AT mamatsieleftheria erythromelalgiainanadolescentfemale AT giorgimelpomeni erythromelalgiainanadolescentfemale AT dinopoulosargirios erythromelalgiainanadolescentfemale AT papaevangelouvasiliki erythromelalgiainanadolescentfemale AT fotislampros erythromelalgiainanadolescentfemale |