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dc.contributor.authorFujita, Marien
dc.contributor.authorKawabata, Hiroshien
dc.contributor.authorOka, Tomomien
dc.contributor.authorHishizawa, Masakatsuen
dc.contributor.authorKitano, Toshiyukien
dc.contributor.authorKondo, Tadakazuen
dc.contributor.authorYamashita, Koheien
dc.contributor.authorYurugi, Kimikoen
dc.contributor.authorHirai, Hideyoen
dc.contributor.authorMaekawa, Tairaen
dc.contributor.authorTakaori-Kondo, Akifumien
dc.contributor.alternative川端, 浩ja
dc.contributor.alternative菱澤, 方勝ja
dc.contributor.alternative北野, 俊行ja
dc.contributor.alternative近藤, 忠一ja
dc.contributor.alternative高折, 晃史ja
dc.date.accessioned2017-07-24T07:57:07Z-
dc.date.available2017-07-24T07:57:07Z-
dc.date.issued2017-
dc.identifier.issn1349-7235-
dc.identifier.urihttp://hdl.handle.net/2433/226544-
dc.description.abstractAutoimmune neutropenia (AIN) is a rare disorder that may cause life-threatening infections. In adults, most cases are secondary to other pathological conditions, and primary AIN is extremely rare. We herein report a case involving a 57-year-old woman diagnosed with AIN. A granulocyte immunofluorescence test detected autoantibodies against human neutrophil antigens in her serum, while various examinations revealed no other causes of neutropenia, suggesting her AIN was primary. She was refractory to granulocyte-colony-stimulating factor but responded to prednisolone. Her neutrophil count remained normal after gradual discontinuation of prednisolone. Diagnostic procedures and optimal treatments for this disorder need to be established.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherJapanese Society of Internal Medicineen
dc.publisher.alternative日本内科学会ja
dc.rights© 2017 The Japanese Society of Internal Medicineen
dc.rightsThe Internal Medicine is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).en
dc.subjecthuman neutrophil antigenen
dc.subjectautoimmune neutropeniaen
dc.subjectgranulocyte-colony-stimulating factoren
dc.titleA rare case of adult autoimmune neutropenia successfully treated with prednisoloneen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleInternal Medicineen
dc.identifier.volume56-
dc.identifier.issue11-
dc.identifier.spage1415-
dc.identifier.epage1419-
dc.relation.doi10.2169/internalmedicine.56.7619-
dc.textversionpublisher-
dc.identifier.pmid28566608-
dcterms.accessRightsopen access-
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