Horny H P, Braumann W, Weiss E, Dietl J, Kaiserling E
Department of Pathology, University of Tübingen, Germany.
Gen Diagn Pathol. 1995 May;141(1):57-60.
The rare case of a stromal Leydig cell tumor of the ovary occurring in a 21-year-old woman who developed signs of virilization during pregnancy is reported. Serum androgen levels were markedly elevated. At cesarean section, a slightly hypotrophic, but otherwise normal, female infant was delivered and a tumor of the right ovary measuring 12 cm in maximum diameter was resected. Histologic examination revealed a sex cord-stromal tumor consisting of spindle-shaped, thecomatous cells and a large number of loosely scattered clusters of large polygonal cells with abundant eosinophilic cytoplasm. Both types of tumor cells were strongly immunoreactive for vimentin, but exhibited no proliferative activity and no overexpression of p53 protein. A few of the polygonal cells contained typical crystalloids of Reinke. Cellular atypia was not a prominent feature, and a diagnosis of benign stromal Leydig cell tumor was established. As expected, 20 months after diagnosis the patient exhibits no signs of recurrence or dissemination. To the best of our knowledge this is only the second case of a stromal Leydig cell tumor occurring in pregnancy to be described.
报告了一例罕见的卵巢间质型莱迪希细胞瘤,发生于一名21岁女性,该女性在孕期出现男性化体征。血清雄激素水平显著升高。剖宫产时,娩出一名轻度发育不良但其他方面正常的女婴,并切除了右侧卵巢一个最大直径为12 cm的肿瘤。组织学检查显示为一种性索间质肿瘤,由梭形的泡膜细胞和大量散在分布的大的多边形细胞簇组成,这些多边形细胞胞质丰富、呈嗜酸性。两种类型的肿瘤细胞波形蛋白免疫反应均呈强阳性,但未表现出增殖活性,也未出现p53蛋白过表达。部分多边形细胞含有典型的雷氏结晶。细胞异型性不显著,诊断为良性间质型莱迪希细胞瘤。正如预期的那样,诊断后20个月,患者未出现复发或转移迹象。据我们所知,这是第二例孕期发生的间质型莱迪希细胞瘤病例报告。