Results of Surgery for a Compound Adrenal Tumor Consisting of Pheochromocytoma and Ganglioneuroblastoma in an Adult : 5-year Follow-up

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抄録

A rare, compound adrenal tumor consisting of ganglioneuroblastoma and pheochroniocytoma was completely resected in an adult woman. Most of the tumor was occupied by the ganglioneuroblastoma component. This ganglioneuroblastoma was an intermixed tumor, which is known to have a favorable prognosis in children. Based on the lack of spread, the resectability of the tumor, and the histology of the ganglioneuroblastoma, no adjuvant therapy was employed. There was no evidence of recurrence at the 5-year follow-up. This suggests that adjuvant therapy may not be necessary in these compound tumors.<br>(Internal Medicine 39: 58-62, 2000)

収録刊行物

  • Internal medicine

    Internal medicine 39(1), 58-61, 2000-01-01

    一般社団法人 日本内科学会

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被引用文献:  1件中 1-1件 を表示

各種コード

  • NII論文ID(NAID)
    10013261122
  • NII書誌ID(NCID)
    AA10827774
  • 本文言語コード
    ENG
  • 資料種別
    NOT
  • ISSN
    09182918
  • NDL 記事登録ID
    4965432
  • NDL 雑誌分類
    ZS21(科学技術--医学--内科学)
  • NDL 請求記号
    Z53-M398
  • データ提供元
    CJP書誌  CJP引用  NDL  J-STAGE 
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