Kalifat R, de Brux J
C.H.I. de Villeneuve St Georges, France.
Int J Gynecol Pathol. 1987;6(4):380-8. doi: 10.1097/00004347-198712000-00010.
We report the light- and electron-microscopic features of a case of sex cord tumor with annular tubules (SCTAT) in a 15-year-old girl. There was no Peutz-Jeghers syndrome (PJS). The tumor was unilateral, 6 cm in diameter, and encapsulated. Optically, the tumor was composed of cellular nests with tubules and hyaline bodies. There was no cytologic evidence of malignancy. Ultrastructural study revealed that the tumor cells were epithelial, with numerous tonofilaments connected to well-formed desmosomes, but neither Charcot-Böttcher crystalloids or filaments nor Reinke crystals were found. The hyaline bodies were composed of packed basement membranes and cellular debris secondary to cellular necrosis, and resembled Call-Exner bodies. There was no true lumen formation. SCTAT showed granulosa cell differentiation and, to a lesser extent, Sertoli cell differentiation. The value of dark cells as evidence of stromal cell origin is questionable, since they might represent metabolic hyperactive cells. We suggest that SCTAT not associated with PJS is a form of granulosa cell tumor, and when associated with PJS is a form of hamartoma.
我们报告了一名15岁女孩的伴有环状小管的性索肿瘤(SCTAT)病例的光镜和电镜特征。该病例无佩-吉综合征(PJS)。肿瘤为单侧性,直径6厘米,有包膜。光学显微镜下,肿瘤由带有小管和透明体的细胞巢组成。没有细胞学证据表明存在恶性肿瘤。超微结构研究显示,肿瘤细胞为上皮性,有大量张力丝连接到发育良好的桥粒,但未发现沙-博晶体或细丝,也未发现雷氏晶体。透明体由堆积的基底膜和细胞坏死后的细胞碎片组成,类似Call-Exner小体。没有真正的管腔形成。SCTAT表现为颗粒细胞分化,在较小程度上也有支持细胞分化。暗细胞作为基质细胞起源证据的价值值得怀疑,因为它们可能代表代谢活跃的细胞。我们认为,不伴有PJS的SCTAT是颗粒细胞瘤的一种形式,而伴有PJS时则是错构瘤的一种形式。