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Complex management of a patient with refractory primary erythromelalgia lacking a SCN9A mutation

A 41-year-old woman presented with burning and erythema in her extremities triggered by warmth and activity, which was relieved by applying ice. Extensive workup was consistent with adult-onset primary erythromelalgia (EM). Several pharmacological treatments were tried including local anesthetics, capsaicin, ziconotide, and dantrolene, all providing 24-48 hours of relief followed by symptom flare. Interventional therapies, including peripheral and sympathetic ganglion blocks, also failed. Thus far, clonidine and ketamine have been the only effective agents for our patient. Genetic testing was negative for an EM-associated mutation in the SCN9A gene, encoding the Na(V)1.7 sodium channel, suggesting a mutation in an alternate gene.

Identiferoai:union.ndltd.org:arizona.edu/oai:arizona.openrepository.com:10150/624081
Date04 1900
CreatorsLow, Sarah, Robbins, Wendye, Tawfik, Vivianne
ContributorsUniv Arizona, Coll Med, Dept Internal Med, Banner Univ Med Ctr
PublisherDOVE MEDICAL PRESS LTD
Source SetsUniversity of Arizona
LanguageEnglish
Detected LanguageEnglish
TypeArticle
Rights© 2017 Low et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms. php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/).
Relationhttps://www.dovepress.com/complex-management-of-a-patient-with-refractory-primary-erythromelalgi-peer-reviewed-article-JPR

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