Hisaoka M, Hashiomoto H, Daimaru Y
Department of Pathology and Oncology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
Pathol Int. 1998 Apr;48(4):307-12. doi: 10.1111/j.1440-1827.1998.tb03911.x.
Two cases of intranodal myofibroblastoma, a rare primary spindle cell tumor of the lymph node, are described. The tumors arose in the inguinal or proximal region of the thigh of one middle-aged and one elderly Japanese male. The tumors were well-demarcated and composed of a fascicular proliferation of spindle cells with focal nuclear palisading and acellular stellate-shaped collagen-rich areas (so-called amianthoid fibers), and were associated with hemorrhagic areas. Immunohistochemically, the tumor cells were positive for vimentin and muscle actin. Together with ultrastructural findings of intracytoplasmic microfilaments with focal densities and profiles of well-developed, rough endoplasmic reticulum, these features reinforced the conclusion of myofibroblastic or smooth muscle differentiation of the tumor cells. One of the tumors was analyzed by flow cytometry and was shown to be DNA diploid. The present report provides clinicopathological findings of the first two Japanese cases of intranodal myofibroblastoma.
本文描述了两例淋巴结内肌成纤维细胞瘤,这是一种罕见的淋巴结原发性梭形细胞肿瘤。肿瘤分别发生于一名中年和一名老年日本男性的腹股沟区或大腿近端。肿瘤边界清晰,由梭形细胞呈束状增生构成,伴有局灶性核栅栏状排列及无细胞的富含胶原的星状区域(所谓石棉样纤维),并伴有出血区。免疫组化显示,肿瘤细胞波形蛋白和肌动蛋白呈阳性。结合肿瘤细胞胞质内有局灶性致密的微丝及发育良好的粗面内质网的超微结构表现,这些特征支持肿瘤细胞肌成纤维细胞或平滑肌分化的结论。其中一例肿瘤经流式细胞术分析显示为DNA二倍体。本报告提供了日本首例两例淋巴结内肌成纤维细胞瘤的临床病理特征。