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pubmed-article:17938019pubmed:dateCreated2007-10-16lld:pubmed
pubmed-article:17938019pubmed:abstractTextHemophagocytic syndrome is a systemic reactive histiocytic proliferative disorder affecting the reticuloendothelial system. Skin lesions develop in 12.5% to 55.6% of the patients. We report a 35-year-old woman with systemic lupus erythematosus and Graves' disease complicated with parvovirus B19-associated hemophagocytic syndrome. She presented with slightly infiltrated erythematous macules and plaques with ulcers on the scalp, face, and back. A skin biopsy specimen taken from an area of facial erythema demonstrated typical phagocytic cells in the skin. Hemophagocytic syndrome-associated specific cutaneous lesions should be included in the differential diagnosis of facial and nonfacial erythema in patients with systemic lupus erythematosus.lld:pubmed
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pubmed-article:17938019pubmed:authorpubmed-author:IizukaHajimeHlld:pubmed
pubmed-article:17938019pubmed:authorpubmed-author:SakaiHiroyuki...lld:pubmed
pubmed-article:17938019pubmed:authorpubmed-author:MiuraTakanori...lld:pubmed
pubmed-article:17938019pubmed:authorpubmed-author:OtsuboSawaSlld:pubmed
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pubmed-article:17938019pubmed:volume57lld:pubmed
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pubmed-article:17938019pubmed:year2007lld:pubmed
pubmed-article:17938019pubmed:articleTitleHemophagocytic syndrome presenting with a facial erythema in a patient with systemic lupus erythematosus.lld:pubmed
pubmed-article:17938019pubmed:affiliationDepartment of Dermatology, Asahikawa City Hospital, Hokkaido, Japan. toko236@syd.odn.ne.jplld:pubmed
pubmed-article:17938019pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:17938019pubmed:publicationTypeCase Reportslld:pubmed