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年轻女性卵巢低分化(小细胞)癌:支持生殖细胞起源的证据

Poorly differentiated (small cell) carcinoma of the ovary in young women: evidence supporting a germ cell origin.

作者信息

Ulbright T M, Roth L M, Stehman F B, Talerman A, Senekjian E K

出版信息

Hum Pathol. 1987 Feb;18(2):175-84. doi: 10.1016/s0046-8177(87)80336-2.

Abstract

The clinical and pathologic features, including immunohistochemistry and electron microscopy, of six cases of poorly differentiated carcinoma of the ovary (small cell carcinoma) are presented. These tumors occurred in six young patients ranging in age from 10 to 24 years. Two patients had hypercalcemia. All tumors were unilateral, and four patients had advanced stage disease at presentation. Histologic features included sheets, nests, and cords of cells in a fibrous stroma, focal microcysts, and a dimorphic population of small and large cells. Eosinophilic, hyaline globules occurred in five cases, intercellular basement membrane-like substance in two cases, and glycogen in all cases. Five of six cases stained strongly for cytokeratin and vimentin; intracytoplasmic laminin was identified in three cases; and three cases were believed to show faint positivity for alpha-1-antitrypsin. Stains for alpha-fetoprotein were negative. Ultrastructural examination of two cases showed granular material in dilated rough endoplasmic reticulum, intermediate filaments, intracytoplasmic dense globules, maculae adherens, and extracellular basement membrane-like material. All of the cases proved rapidly fatal despite various therapies, as did a histologically similar testicular tumor that was admixed with seminoma and teratoma. We interpret these findings to indicate that this ovarian cancer is most likely of germ cell origin, and it may be related to yolk sac tumor, although it is clearly distinct from the classical yolk sac tumor.

摘要

本文报告了6例低分化卵巢癌(小细胞癌)的临床和病理特征,包括免疫组织化学和电子显微镜检查结果。这些肿瘤发生在6名年龄在10岁至24岁之间的年轻患者身上。两名患者出现高钙血症。所有肿瘤均为单侧性,4例患者就诊时已处于晚期。组织学特征包括纤维性间质中细胞的片状、巢状和索状排列、局灶性微囊肿以及大小细胞的双相群体。5例出现嗜酸性透明小球,2例出现细胞间基底膜样物质,所有病例均有糖原。6例中有5例细胞角蛋白和波形蛋白染色强阳性;3例在胞质内鉴定出层粘连蛋白;3例被认为α-1抗胰蛋白酶呈弱阳性。甲胎蛋白染色为阴性。2例的超微结构检查显示扩张的粗面内质网中有颗粒物质、中间丝、胞质内致密小球、黏着斑和细胞外基底膜样物质。尽管采用了各种治疗方法,但所有病例均迅速死亡,与混合有精原细胞瘤和畸胎瘤的组织学相似的睾丸肿瘤情况相同。我们认为这些发现表明这种卵巢癌很可能起源于生殖细胞,可能与卵黄囊瘤有关,尽管它显然与经典的卵黄囊瘤不同。

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