日本小児外科学会雑誌
Online ISSN : 2187-4247
Print ISSN : 0288-609X
ISSN-L : 0288-609X
転移再発を繰り返した卵巣原発類胎芽併合奇形腫の1例
上野 滋石田 治雄林 奐鎌形 正一郎杉谷 一宏村越 孝次初鹿野 浩
著者情報
ジャーナル フリー

1986 年 22 巻 1 号 p. 99-105

詳細
抄録
A 14-year-old girl was found to have right ovarian tumor of 12×6×3cm, which is not associated with any apparent metastasis at her first laparotomy. Although right oophorectomy was performed successfully, tumors were found disseminated into the abdominal cavity 3 months later, accompanied with the increased serum alpha-feto protein(AFP)level. In spite of the vigorous chemotherapy using vincristine, actinomycin-D, and cyclophosphamide, tumor growth continued. Repeated tumor resections were performed to eliminate tumors. After the final resection serum AFP level decreased to normal and no tumor regrowth has been detected. Microscopic examination of the resected tumors demonstrated that the primary tumor was composed of the tridermal immature tissues containin some embryo id bodies. Metastatic tumors were mostly found as the peritoneal dissemination but a few lymph node metastases were also found. All metastatic tumors were also composed of mature and immature tissues of the tridermal origin, but they did not contain any tissue suggesting malignancy or embryoid bodies. Immunoperoxidase techniques revealed that AFP was located at the yolk sac tissue in the embryoid body, at the liver tissue-like cell clusters, and at the tubular structures of immature endodermal origin. Embryoid body may be the structure which suggests the presence of the totipotent cells, which can metastasize and differentiate into any embryonic or adult tissues. These totipotential cells may not necessarrily be of malignant nature. AFP can be found in the benign teratoma when it contains any tissne that can produce AFP in the course of fetal development.
著者関連情報
© 1986 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
前の記事 次の記事
feedback
Top