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pubmed-article:15609644pubmed:issue11lld:pubmed
pubmed-article:15609644pubmed:dateCreated2004-12-21lld:pubmed
pubmed-article:15609644pubmed:abstractTextErythromelalgia is known as a rare syndrome of unknown etiology, characterized by redness with burning pain, edema associated with increased skin temperature in the upper and/or lower extremities. Various treatments such as drug therapies and sympathetic blockade were reported. We report two cases including a 57-year-old woman and a 64-year-old woman, showing the successful clinical outcome by bilateral thoracoscopic sympathectomy.lld:pubmed
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pubmed-article:15609644pubmed:authorpubmed-author:ShimizuKazuoKlld:pubmed
pubmed-article:15609644pubmed:authorpubmed-author:NakajimaYukiYlld:pubmed
pubmed-article:15609644pubmed:authorpubmed-author:SakamotoAtsuh...lld:pubmed
pubmed-article:15609644pubmed:authorpubmed-author:KoizumiKiyosh...lld:pubmed
pubmed-article:15609644pubmed:authorpubmed-author:HirataTomomiTlld:pubmed
pubmed-article:15609644pubmed:authorpubmed-author:HiraiKyojiKlld:pubmed
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pubmed-article:15609644pubmed:year2004lld:pubmed
pubmed-article:15609644pubmed:articleTitleSuccessful thoracoscopic sympathectomy for primary erythromelalgia in the upper extremities.lld:pubmed
pubmed-article:15609644pubmed:affiliationDepartment of Surgery II, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, Tokyo 113-8603, Japan.lld:pubmed
pubmed-article:15609644pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15609644pubmed:publicationTypeCase Reportslld:pubmed