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タイトル: 腎原発未分化神経外胚葉性腫瘍の1例
その他のタイトル: Primitive Neuroectodermal Tumor of Kidney : A Case Report
著者: 堤, 尚史  KAKEN_name
住吉, 崇幸  KAKEN_name
岡村, 基弘  KAKEN_name
仲島, 義治  KAKEN_name
岩村, 浩志  KAKEN_name
光森, 健二  KAKEN_name
西村, 一男  KAKEN_name
新宅, 雅幸  KAKEN_name
小山, 貴  KAKEN_name
松井, 祐亮  KAKEN_name
渡邊, 光正  KAKEN_name
著者名の別形: Tsutsumi, Naofumi
Sumiyoshi, Takayuki
Okamura, Motohiro
Nakashima, Yoshiharu
Iwamura, Hiroshi
Mitsumori, Kenji
Nishimura, Kazuo
Shintaku, Masayuki
Koyama, Takashi
Matsui, Yusuke
Watanabe, Mitsumasa
キーワード: Primitive neuroectodermal tumor
Kidney
発行日: Jun-2013
出版者: 泌尿器科紀要刊行会
誌名: 泌尿器科紀要
巻: 59
号: 6
開始ページ: 363
終了ページ: 367
抄録: A 16-year-old man was referred to our hospital for asymptomatic gross hematuria. The findings of abdominal ultrasonography were normal. A month later, gross hematuria disappeared, and he was not followed after that. A month later, the patient was taken to our hospital in an ambulance for severe back pain and recurring gross hematuria. Computed tomography (CT) revealed a large right renal tumor with tumor thrombus penetrating inside the inferior vena cava. The patient underwent radical nephrectomy and embolectomy. The pathological diagnosis of the tumor was diagnosed as primitive neuroectodermal tumor (PNET) of kidney by immunostaining and gene analysis. We started adjuvant chemotherapy soon after the operation. However, at 10 months after, multiple pulmonary metastases were detected. The patient was treated with salvage chemotherapy, surgery and irradiation therapy as combined modality therapy. Nevertheless, he died 18 months after the diagnosis.
著作権等: 許諾条件により本文は2014-07-01に公開
URI: http://hdl.handle.net/2433/175712
PubMed ID: 23827869
出現コレクション:Vol.59 No.6

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