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子宫平滑肌瘤中的骨骼肌样细胞和横纹肌样细胞。

Skeletal muscle-like and rhabdoid cells in uterine leiomyomas.

作者信息

Parker Robin L, Young Robert H, Clement Philip B

机构信息

Department of Pathology and Laboratory Medicine, Calgary Laboratory Services and University of Calgary, Calgary, Alberta, Canada.

出版信息

Int J Gynecol Pathol. 2005 Oct;24(4):319-25. doi: 10.1097/01.pgp.0000177647.45890.b5.

Abstract

We describe eight unusual uterine leiomyomas characterized by a component of cells that suggested skeletal muscle differentiation or resembled the rhabdoid cells of extrarenal rhabdoid tumors. All of the tumors were referred because of problems in differential diagnosis, particularly distinction from an epithelioid smooth muscle tumor, a smooth muscle tumor of uncertain malignant potential, or a tumor with skeletal muscle differentiation. The patients were aged 27 to 50 (mean, 38) years, and the presenting clinical features and gross appearance of the tumors were similar to those of typical uterine leiomyomas. On microscopic examination, seven of the tumors were well circumscribed, whereas one showed slight irregularity of its margin. The characteristic feature of the tumors was a variable number of rounded, polygonal, or strap-shaped cells with abundant deeply eosinophilic cytoplasm and fibrillar, or occasionally hyaline, intracytoplasmic globules. Cytoplasmic cross-striations were not identified. The cells usually had eccentric, round-to-oval nuclei with conspicuous nucleoli. A variable number of the rhabdoid/skeletal muscle-like cells, as well as cells without these features, contained multiple or multilobed, pleomorphic, hyperchromatic nuclei, thus qualifying the tumors as leiomyomas with bizarre nuclei. Foci of hydropic change were present in all of the tumors. The mitotic index was low (<1 mitotic figure/10 high-power fields) and necrosis was absent in all the tumors. The rhabdoid/skeletal muscle-like cells were immunoreactive for desmin and h-caldesmon, but not for cytokeratin (AE1/AE3) or skeletal muscle markers (myoglobin, Myo-D1, or myogenin). Intracytoplasmic whorls of intermediate filaments were observed in the cells of one case examined by electron microscopy; there was no ultrastructural evidence of skeletal muscle differentiation. The histologic, immunohistochemical, and ultrastructural features indicated that the peculiar cells in these leiomyomas likely represented smooth muscle cells with an unusual phenotype rather than the cells of uterine tumors with skeletal muscle differentiation, extrarenal rhabdoid tumors, or epithelioid smooth muscle tumors. An association with leiomyomas with bizarre nuclei also was suggested.

摘要

我们描述了8例不寻常的子宫平滑肌瘤,其特征是含有提示骨骼肌分化的细胞成分或类似于肾外横纹肌样瘤的横纹肌样细胞。所有这些肿瘤均因鉴别诊断问题而被转诊,特别是与上皮样平滑肌瘤、恶性潜能不确定的平滑肌瘤或具有骨骼肌分化的肿瘤相鉴别。患者年龄在27至50岁(平均38岁)之间,肿瘤的临床表现和大体外观与典型子宫平滑肌瘤相似。显微镜检查显示,7例肿瘤边界清晰,而1例边缘略有不规则。这些肿瘤的特征性表现是数量不等的圆形、多边形或带状细胞,胞质丰富且嗜酸性深染,含有纤维状或偶尔为透明的胞质内小球。未发现胞质横纹。这些细胞通常有偏心的圆形至椭圆形核,核仁明显。数量不等的横纹肌样/骨骼肌样细胞以及无这些特征的细胞含有多个或多叶状、多形性、深染的核,因此这些肿瘤符合具有奇异核的平滑肌瘤。所有肿瘤均有水肿变性灶。有丝分裂指数低(<1个有丝分裂象/每10个高倍视野),所有肿瘤均无坏死。横纹肌样/骨骼肌样细胞对结蛋白和h-钙调蛋白呈免疫反应,但对细胞角蛋白(AE1/AE3)或骨骼肌标志物(肌红蛋白、Myo-D1或肌生成素)无反应。在1例经电子显微镜检查的病例中,细胞内可见中间丝的胞质涡旋;无骨骼肌分化的超微结构证据。组织学、免疫组化和超微结构特征表明,这些平滑肌瘤中的特殊细胞可能代表具有异常表型的平滑肌细胞,而非具有骨骼肌分化的子宫肿瘤、肾外横纹肌样瘤或上皮样平滑肌瘤的细胞。还提示与具有奇异核的平滑肌瘤有关。

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