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节段性胶质瘤病与甲胎蛋白产生:I级卵巢畸胎瘤的两个不寻常特征。

Nodal gliomatosis and alpha-fetoprotein production. Two unusual facets of grade I ovarian teratoma.

作者信息

Perrone T, Steiner M, Dehner L P

出版信息

Arch Pathol Lab Med. 1986 Oct;110(10):975-7.

PMID:2429641
Abstract

We describe the case of a 10-month-old infant who had a grade I solid teratoma of the ovary. It is remarkable that the tumor was accompanied by nodal gliomatosis and elevated serum alpha-fetoprotein (AFP) level. To our knowledge, this is the first description of nodal gliomatosis in the absence of gliomatosis peritonei, and the fifth report of elevated serum AFP with a pure teratoma. Like gliomatosis peritonei, nodal gliomatosis appears to be a benign condition, requiring no adjuvant therapy. The nature of the nodal implants was confirmed by positive immunoreactivity for glial fibrillary acidic protein. By a similar method, AFP was found in the primary tumor in cells lining yolk-sac-like vesicles and intestinal-type glands.

摘要

我们描述了一名10个月大患有I级卵巢实性畸胎瘤婴儿的病例。值得注意的是,该肿瘤伴有淋巴结胶质瘤病和血清甲胎蛋白(AFP)水平升高。据我们所知,这是首例在无腹膜胶质瘤病情况下对淋巴结胶质瘤病的描述,也是第五例报道的纯畸胎瘤伴血清AFP升高的病例。与腹膜胶质瘤病一样,淋巴结胶质瘤病似乎是一种良性疾病,无需辅助治疗。通过对胶质纤维酸性蛋白免疫反应阳性证实了淋巴结植入物的性质。通过类似方法,在原发性肿瘤中卵黄囊样小泡和肠型腺体的衬里细胞中发现了AFP。

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