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タイトル: | 急激な経過をたどった腎原発血管肉腫の1例 |
その他のタイトル: | A Case of Primary Renal Angiosarcoma with a Rapidly Worsening Course |
著者: | 中保, 良太 清水, 洋祐 山口, 立樹 請田, 翔子 宇都宮, 紀明 浅井, 沙月 石原, 美佐 橋本, 公夫 金丸, 聰淳 |
著者名の別形: | NAKAYASU, Ryota SHIMIZU, Yousuke YAMAGUCHI, Ritsuki UKETA, Shoko UTSUNOMIYA, Noriaki ASAI, Satsuki ISHIHARA, Misa HASHIMOTO, Kimio KANAMARU, Sojun |
キーワード: | Angiosarcoma Kidney |
発行日: | 30-Sep-2021 |
出版者: | 泌尿器科紀要刊行会 |
誌名: | 泌尿器科紀要 |
巻: | 67 |
号: | 9 |
開始ページ: | 413 |
終了ページ: | 417 |
抄録: | A 69-year-old man presented with left flank pain and underwent a computed tomographic scan, which revealed a large left renal mass of 16×9×5 cm. A left nephrectomy was performed. Pathological analysis revealed that the tumor was consistent with angiosarcoma of the left kidney with a negative surgical margin. He received combination therapy with radiation therapy and four courses of chemotherapy with doxorubicin and ifosfamide. However, he died 10 months after surgery because of pleural dissemination and peritoneal dissemination. Primary renal angiosarcoma is an extremely rare and highly aggressive tumor with a dismal survival rate, and a satisfactory surgical margin is necessary for its successful treatment. If primary renal angiosarcoma is suspected, biopsy may be considered before surgery. Primary renal angiosarcoma treatment with combination therapy of surgery, radiotherapy, and chemotherapy by a specialist multidisciplinary team with experience and expertise in sarcoma is preferable. Development of therapy for angiosarcoma is awaited. |
著作権等: | 許諾条件により本文は2022-10-01に公開 |
DOI: | 10.14989/ActaUrolJap_67_9_413 |
URI: | http://hdl.handle.net/2433/265463 |
PubMed ID: | 34610706 |
出現コレクション: | Vol.67 No.9 |
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