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タイトル: 膀胱原発神経鞘腫の1例
その他のタイトル: A Case of Primary Schwannoma of the Urinary Bladder
著者: 松本, 吉隆  KAKEN_name
和久, 夏衣  KAKEN_name
河合, 弘二  KAKEN_name
池田, 篤史  KAKEN_name
木村, 友和  KAKEN_name
石塚, 竜太郎  KAKEN_name
小島, 崇宏  KAKEN_name
末富, 崇弘  KAKEN_name
常樂, 晃  KAKEN_name
宮崎, 淳  KAKEN_name
坂下, 麻衣  KAKEN_name
西山, 博之  KAKEN_name
著者名の別形: Matsumoto, Yoshitaka
Waku, Natsui
Kawai, Koji
Ikeda, Atsushi
Kimura, Tomokazu
Ishitsuka, Ryutaro
Kojima, Takahiro
Suetomi, Takahiro
Joraku, Akira
Miyazaki, Jun
Sakashita, Mai
Nishiyama, Hiroyuki
キーワード: Urinary bladder
Schwannoma
発行日: 31-Aug-2017
出版者: 泌尿器科紀要刊行会
誌名: 泌尿器科紀要
巻: 63
号: 8
開始ページ: 323
終了ページ: 328
抄録: A 68-year-old woman presented with a bladder tumor. She was asymptomatic, and the tumor was incidentally detected with radiological imaging performed during treatment of cervical cancer. Magnetic resonance imaging and computed tomography revealed a solitary submucosal tumor located in the anterior wall of the urinary bladder, with homogeneous contrast enhancement. Cystoscopy showed a submucosal tumor covered by normal mucosa. A paraganglioma was considered in the differential diagnosis, but symptoms suggesting hypercatecholaminemia were not apparent. Moreover, she did not have a family history or symptoms associated with neurofibromatosis-1 (NF-1). She underwent partial cystectomy with a preliminary diagnosis of submucosal bladder tumor. Histopathological diagnosis confirmed a schwannoma arising from the bladder wall. She was followed up without intravesical recurrence or metastases for 6 months. In the literature, only 12 cases of bladder schwannoma have been reported. There was no reported family history or symptoms associated with NF-1 in any of the cases. Although the number of cases is limited, literature review showed a favorable prognosis for bladder schwannoma with local tumor resection in patients without NF-1.
著作権等: 許諾条件により本文は2018/09/01に公開
DOI: 10.14989/ActaUrolJap_63_8_323
URI: http://hdl.handle.net/2433/227093
PubMed ID: 28889717
出現コレクション:Vol.63 No.8

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