{"created":"2023-05-15T16:37:10.354352+00:00","id":10466,"links":{},"metadata":{"_buckets":{"deposit":"058dafd2-1a8a-474a-8665-79329b9ce017"},"_deposit":{"created_by":2,"id":"10466","owners":[2],"pid":{"revision_id":0,"type":"depid","value":"10466"},"status":"published"},"_oai":{"id":"oai:nagasaki-u.repo.nii.ac.jp:00010466","sets":["29:30:1713167819629:802"]},"author_link":["41524","41523","41527","41525","41522","41521","41526"],"item_3_biblio_info_6":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2012-07","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"2","bibliographicPageEnd":"63","bibliographicPageStart":"57","bibliographicVolumeNumber":"57","bibliographic_titles":[{"bibliographic_title":"Acta medica Nagasakiensia"}]}]},"item_3_description_4":{"attribute_name":"抄録","attribute_value_mlt":[{"subitem_description":"Rosai-Dorfman disease (RDD) is an uncommon, non-neoplastic benign lymphoproliferative disease characterized by prominent,\npainless cervical lymphadenopathy with fever and leukocytosis. RDD is histologically characterized by emperipolesis,\nwhere large histiocytes become infiltrated with lymphocytes and plasma cells. Intracranial RDD is extremely rare. Only 79\ncases have been reported, including the present case. Intracranial RDD is associated with headaches, seizures, and numbness\ncaused by increased intracranial pressure. A 67-year-old Japanese woman presented with dizziness and was diagnosed\nwith a tumor in the cerebral falx. The preoperative radiological diagnosis was meningioma. She had no lymphadenopathy. The\npatient underwent a craniotomy and tumor resection. The tumor consisted of lymphoid tissue with scattered lymph follicles.\nThe infiltrating histiocytes showed emperipolesis. The histiocytes were immunoreactive for S-100 protein and CD68 and negative\nfor CD1a, leading to the diagnosis of intracranial RDD. The postoperative course was uneventful without further therapy.\nThe dizziness had not re-appeared and MRI demonstrated no recurrence of tumors for 7 months. Intracranial RDD shows a\nmale predominance and occurs later in life than nodal RDD. The clinical manifestations and prognosis are variable depending\non the location of the tumor and treatment. Most intracranial RDD have a benign course, but long-term follow-up is important,\nbecause recurrence has been observed.","subitem_description_type":"Abstract"}]},"item_3_description_64":{"attribute_name":"引用","attribute_value_mlt":[{"subitem_description":"Acta medica Nagasakiensia, 57(2), pp.57-63; 2012","subitem_description_type":"Other"}]},"item_3_publisher_33":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"Nagasaki University School of Medicine"}]},"item_3_source_id_10":{"attribute_name":"書誌レコードID","attribute_value_mlt":[{"subitem_source_identifier":"AA00508430","subitem_source_identifier_type":"NCID"}]},"item_3_source_id_7":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"00016055","subitem_source_identifier_type":"ISSN"}]},"item_3_text_62":{"attribute_name":"sortkey","attribute_value_mlt":[{"subitem_text_value":"6"}]},"item_3_text_63":{"attribute_name":"出版者別言語","attribute_value_mlt":[{"subitem_text_value":"長崎大学医学部"}]},"item_3_version_type_16":{"attribute_name":"著者版フラグ","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_970fb48d4fbd8a85","subitem_version_type":"VoR"}]},"item_creator":{"attribute_name":"著者","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"Yamauchi, Taishi"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Hayashi, Tomayoshi"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Matsuo, Takayuki"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Matsumoto, Miki"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Kinoshita, Naoe"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Abe, Kuniko"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Nagata, Izumi"}],"nameIdentifiers":[{}]}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2020-12-22"}],"displaytype":"detail","filename":"ActMed57_57.pdf","filesize":[{"value":"311.5 kB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"ActMed57_57.pdf","url":"https://nagasaki-u.repo.nii.ac.jp/record/10466/files/ActMed57_57.pdf"},"version_id":"693369d6-6bce-46f5-9fca-b08dd9124661"}]},"item_keyword":{"attribute_name":"キーワード","attribute_value_mlt":[{"subitem_subject":"Rosai-Dorfman disease","subitem_subject_scheme":"Other"},{"subitem_subject":"intracranial","subitem_subject_scheme":"Other"},{"subitem_subject":"sinus histiocytosis with massive lymphadenopathy","subitem_subject_scheme":"Other"},{"subitem_subject":"emperipolesis","subitem_subject_scheme":"Other"},{"subitem_subject":"literature review","subitem_subject_scheme":"Other"}]},"item_language":{"attribute_name":"言語","attribute_value_mlt":[{"subitem_language":"eng"}]},"item_resource_type":{"attribute_name":"資源タイプ","attribute_value_mlt":[{"resourcetype":"departmental bulletin paper","resourceuri":"http://purl.org/coar/resource_type/c_6501"}]},"item_title":"Intracranial Rosai-Dorfman Disease - a Case Report and a Review of the Literature","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"Intracranial Rosai-Dorfman Disease - a Case Report and a Review of the Literature"}]},"item_type_id":"3","owner":"2","path":["802"],"pubdate":{"attribute_name":"公開日","attribute_value":"2012-08-07"},"publish_date":"2012-08-07","publish_status":"0","recid":"10466","relation_version_is_last":true,"title":["Intracranial Rosai-Dorfman Disease - a Case Report and a Review of the Literature"],"weko_creator_id":"2","weko_shared_id":2},"updated":"2024-04-16T05:30:41.541941+00:00"}