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Intracranial Rosai-Dorfman Disease - a Case Report and a Review of the Literature
http://hdl.handle.net/10069/28963
http://hdl.handle.net/10069/28963af3b4077-01c3-4987-8b0d-389bb91c6d7b
| 名前 / ファイル | ライセンス | アクション |
|---|---|---|
ActMed57_57.pdf (311.5 kB)
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| Item type | 紀要論文 / Departmental Bulletin Paper(1) | |||||
|---|---|---|---|---|---|---|
| 公開日 | 2012-08-07 | |||||
| タイトル | ||||||
| タイトル | Intracranial Rosai-Dorfman Disease - a Case Report and a Review of the Literature | |||||
| 言語 | ||||||
| 言語 | eng | |||||
| キーワード | ||||||
| 主題Scheme | Other | |||||
| 主題 | Rosai-Dorfman disease | |||||
| キーワード | ||||||
| 主題Scheme | Other | |||||
| 主題 | intracranial | |||||
| キーワード | ||||||
| 主題Scheme | Other | |||||
| 主題 | sinus histiocytosis with massive lymphadenopathy | |||||
| キーワード | ||||||
| 主題Scheme | Other | |||||
| 主題 | emperipolesis | |||||
| キーワード | ||||||
| 主題Scheme | Other | |||||
| 主題 | literature review | |||||
| 資源タイプ | ||||||
| 資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
| 資源タイプ | departmental bulletin paper | |||||
| 著者 |
Yamauchi, Taishi
× Yamauchi, Taishi× Hayashi, Tomayoshi× Matsuo, Takayuki× Matsumoto, Miki× Kinoshita, Naoe× Abe, Kuniko× Nagata, Izumi |
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| 抄録 | ||||||
| 内容記述タイプ | Abstract | |||||
| 内容記述 | Rosai-Dorfman disease (RDD) is an uncommon, non-neoplastic benign lymphoproliferative disease characterized by prominent, painless cervical lymphadenopathy with fever and leukocytosis. RDD is histologically characterized by emperipolesis, where large histiocytes become infiltrated with lymphocytes and plasma cells. Intracranial RDD is extremely rare. Only 79 cases have been reported, including the present case. Intracranial RDD is associated with headaches, seizures, and numbness caused by increased intracranial pressure. A 67-year-old Japanese woman presented with dizziness and was diagnosed with a tumor in the cerebral falx. The preoperative radiological diagnosis was meningioma. She had no lymphadenopathy. The patient underwent a craniotomy and tumor resection. The tumor consisted of lymphoid tissue with scattered lymph follicles. The infiltrating histiocytes showed emperipolesis. The histiocytes were immunoreactive for S-100 protein and CD68 and negative for CD1a, leading to the diagnosis of intracranial RDD. The postoperative course was uneventful without further therapy. The dizziness had not re-appeared and MRI demonstrated no recurrence of tumors for 7 months. Intracranial RDD shows a male predominance and occurs later in life than nodal RDD. The clinical manifestations and prognosis are variable depending on the location of the tumor and treatment. Most intracranial RDD have a benign course, but long-term follow-up is important, because recurrence has been observed. |
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| 書誌情報 |
Acta medica Nagasakiensia 巻 57, 号 2, p. 57-63, 発行日 2012-07 |
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| ISSN | ||||||
| 収録物識別子タイプ | ISSN | |||||
| 収録物識別子 | 00016055 | |||||
| 書誌レコードID | ||||||
| 収録物識別子タイプ | NCID | |||||
| 収録物識別子 | AA00508430 | |||||
| 著者版フラグ | ||||||
| 出版タイプ | VoR | |||||
| 出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
| 出版者 | ||||||
| 出版者 | Nagasaki University School of Medicine | |||||
| 出版者別言語 | ||||||
| 値 | 長崎大学医学部 | |||||
| sortkey | ||||||
| 値 | 6 | |||||
| 引用 | ||||||
| 内容記述タイプ | Other | |||||
| 内容記述 | Acta medica Nagasakiensia, 57(2), pp.57-63; 2012 | |||||
