Bolen J W
Am J Clin Pathol. 1981 Apr;75(4):565-73. doi: 10.1093/ajcp/75.4.565.
A mixed germ cell-sex cord stromal tumor and a gonadoblastoma were examined by light and electron microscopy. The mixed germ cell-sex cord stromal tumor occurred in a normal adult male, father of two children, whereas the gonadoblastoma arose in a dysgenetic gonad of a phenotypic female. The light-microscopic appearance of the gonadoblastoma was distinctive for its organoid arrangement of sex cord cells and germ cells and its pattern of secondary alterations resultings in mulberry areas of hyalinization and calcification. The ultrastructural features of the sex cord stromal cells were similar in both lesions; however, the germ cells of the mixed germ cell-sex cord stromal tumor were distinctive for the presence of true intercellular bridges. This finding suggested primary spermatogenic differentiation. It was concluded that the mixed germ cell-sex cord stromal tumor was clinically and pathologically distinct from the more widely recognized gonadoblastoma.
对一例混合性生殖细胞-性索间质肿瘤和一例性腺母细胞瘤进行了光镜和电镜检查。混合性生殖细胞-性索间质肿瘤发生于一名正常成年男性,育有两个孩子,而性腺母细胞瘤则发生于一名表型女性的发育异常性腺中。性腺母细胞瘤的光镜表现独特,其性索细胞和生殖细胞呈器官样排列,继发改变导致桑葚样玻璃样变和钙化区域。两种病变中性索间质细胞的超微结构特征相似;然而,混合性生殖细胞-性索间质肿瘤的生殖细胞因存在真正的细胞间桥而具有独特性。这一发现提示原发性生精分化。结论是,混合性生殖细胞-性索间质肿瘤在临床和病理上与更广泛认可的性腺母细胞瘤不同。