[Juvenile granulosa-cell tumor of the ovary. Immunohistochemical and ultrastructural study].

Archivos de investigacion medica Pub Date : 1990-10-01
C Astengo-Osuna
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Abstract

In 1977 Scully first described the juvenile granulosa cell tumor of the ovary (JGCT) as a special variation of the granulosa cells tumor, which occurs in the two first decades of life, and 97% of the cases show characteristic microscopic and histological features. Five previous cases have been reported concerning the ultramicroscopic characteristics of this ovarian neoplasia. The purpose of this paper is to report the immunohistochemical and ultrastructural characteristics in a case of OJCGT which occurred in a four year old girl with isosexual precocious pseudopuberty. The presence of vimentin and absence of keratin was proven immunohistochemically in this ovarian neoplasia. Intermediate filaments were found ultrastructurally. The combined use of immunohistochemical and ultrastructural techniques has proven to be of extraordinary usefulness for the differential diagnosis between epithelial and non epithelial ovarian tumors and adds a new and highly specific method to characterize and differentiate the cells of embryonic carcinoma, choriocarcinomas and endodermal sinus tumors which are keratin positive.

卵巢幼年颗粒细胞瘤。免疫组织化学和超微结构研究]。
1977年,Scully首次将卵巢幼年颗粒细胞瘤(JGCT)描述为颗粒细胞瘤的一种特殊变异,发生在生命的前20年,97%的病例表现出特征性的显微镜和组织学特征。已有5例病例报道了这种卵巢肿瘤的超微特征。本文报告1例4岁女童同性性早熟性假性囊肿的免疫组织化学和超微结构特征。免疫组织化学证实卵巢肿瘤中有静脉蛋白存在,角蛋白缺失。超微结构上发现中间细丝。免疫组织化学和超微结构技术的联合应用已被证明对卵巢上皮性和非上皮性肿瘤的鉴别诊断非常有用,并为角蛋白阳性的胚胎癌、绒毛膜癌和内胚层窦瘤的细胞特征和分化提供了一种新的、高度特异性的方法。
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