日本小児外科学会雑誌
Online ISSN : 2187-4247
Print ISSN : 0288-609X
ISSN-L : 0288-609X
III-19) 組織像および臨床的要因よりみた神経芽腫, 神経節芽腫の予後(III 病理学的に興味ある症例, <特集>神経芽腫群腫瘍の臨床)
千葉 庸夫嶋田 博行W.A.Jr. Newton
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1984 年 20 巻 1 号 p. 62-65

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Histological findings of neuroblastic tumors of 313 patients who had no treatment before surgery were compared with their results. They were divided into 5 groups by the distribution of the neuroblastic cells and mitotic rates. Well differentiated type, intermixed type(tumor of fully differentiated ganglioneuromatous tissue with presence of multiple microscopic foci of neuroblastic cell nests), and diffuse neuroblastic type with a small number of mitotic cells(less than 200 of 5,000 tumor cells) are apparently have better prognosis than focal nodular type(discrete nodules of immature cells with capsular structure which are seen in gross findings in ganglioneuromatous tissue), or other diffuse type.
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© 1984 特定非営利活動法人 日本小児外科学会

この記事はクリエイティブ・コモンズ [表示 - 非営利 - 継承 4.0 国際]ライセンスの下に提供されています。
https://creativecommons.org/licenses/by-nc-sa/4.0/deed.ja
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