Renshaw A A, Gordon M, Corless C L
Department of Pathology, Brigham and Women's Hospital, Boston, MA 02115, USA.
Mod Pathol. 1997 Jul;10(7):693-700.
Unclassified sex cord-stromal tumors (SCSTs) of the testis comprised predominantly of spindle cells can be difficult to classify. To achieve better definition of these tumors, we examined the histologic, histochemical, and ultrastructural features of four unclassified SCSTs with spindle-cell features, and compared their immunohistochemical features with those of 24 other SCSTs of the testis and ovary. Three of the spindle-cell tumors were composed of relatively short spindled cells with prominent nuclear grooves and intermixed epithelioid cells. All of the three were located adjacent to the rete testis. The fourth case consisted of elongate spindle cells that were reminiscent of smooth muscle. In all of the four cases, reticulin enveloped aggregates of cells of various sizes but not individual cells. Ultrastructural analysis of two of the spindle-cell tumors revealed desmosomes, numerous thin filaments, and focal dense-bodies. Immunohistochemically, all of the four tumors were reactive for S-100 protein and smooth muscle actin. Staining for S-100 protein and smooth muscle actin was also observed in three of six granulosa cell tumors and both juvenile granulosa cell tumors. Although variable staining for S-100 protein was found in 5 of the 12 other SCSTs (4 Leydig cell, 6 Sertoli-Leydig cell, and 2 unclassifiable ovarian SCSTs), reactivity for smooth muscle actin was present in only 1 Sertoli-Leydig cell tumor. In contrast, all of the four ovarian fibromas/thecomas were reactive for smooth muscle actin but failed to stain for S-100 protein. Taken together, the histologic, histochemical, immunohistochemical, and ultrastructural features of the spindle-cell tumors are similar to those of granulosa cell tumors. Reactivity for S-100 protein and smooth muscle actin is characteristic of these tumors. These tumors should be distinguished from other unclassified SCSTs.
以梭形细胞为主的睾丸未分类性索间质肿瘤(SCSTs)可能难以分类。为了更好地界定这些肿瘤,我们检查了4例具有梭形细胞特征的未分类SCSTs的组织学、组织化学和超微结构特征,并将其免疫组化特征与另外24例睾丸和卵巢SCSTs的特征进行了比较。3例梭形细胞肿瘤由相对短的梭形细胞组成,具有明显的核沟,并伴有上皮样细胞。这3例均位于睾丸网附近。第4例由细长的梭形细胞组成,类似平滑肌。在所有4例中,网硬蛋白包绕各种大小的细胞团,但不包绕单个细胞。对其中2例梭形细胞肿瘤的超微结构分析显示有桥粒、大量细肌丝和局灶性致密小体。免疫组化方面,所有4例肿瘤对S-100蛋白和平滑肌肌动蛋白均呈阳性反应。6例颗粒细胞瘤中的3例以及2例幼年型颗粒细胞瘤也观察到S-100蛋白和平滑肌肌动蛋白染色。虽然在另外12例SCSTs中的5例(4例睾丸间质细胞瘤、6例支持-间质细胞瘤和2例无法分类的卵巢SCSTs)发现S-100蛋白染色存在差异,但仅1例支持-间质细胞瘤对平滑肌肌动蛋白呈阳性反应。相比之下,所有4例卵巢纤维瘤/卵泡膜瘤对平滑肌肌动蛋白呈阳性反应,但对S-100蛋白不着色。综上所述,梭形细胞肿瘤的组织学、组织化学、免疫组化和超微结构特征与颗粒细胞瘤相似。对S-100蛋白和平滑肌肌动蛋白呈阳性反应是这些肿瘤的特征。这些肿瘤应与其他未分类的SCSTs相鉴别。