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软组织巨细胞瘤。一项超微结构研究。

Giant cell tumor of soft parts. An ultrastructural study.

作者信息

van Haelst U J, de Haas van Dorsser A H

出版信息

Virchows Arch A Pathol Anat Histol. 1976 Sep 21;371(3):199-217. doi: 10.1007/BF00433068.

Abstract

The light-microscopic and ultrastructural findings in a case of so-called giant cell tumor of soft parts, localized at the dorsal side of the left foot of a 23-years-old male are described. An amputation of the lower extremity was performed and subsequently chemotherapy with adriamycin was given for 3 months. Despite the histology and cytologic malignant appearance and the evident vascular invasion, already present at the time of the first excision, the last known status 2 years later seems favorable. There are no pathologic lymph nodes in the groins and no signs of metastases on chest X-rays. From the electron-microscope study no definite conclusion can be drawn as regards the histogenesis of this tumor. we feel, as do others, that many of the principal mononuclear tumor cells are poorly differentiated mesenchymal cells. Some of the neoplastic cells, however, show ultrastructural features suggestive of chondro- or osteoblasts (a well-developed r.e.r. containing electron-dense material; multiple Golgi complexes; masses of glycogen; interdigitating cell membrane villi; cytoplasmic filaments; an extracellular amorphous matrix). Some of the larger tumor cells have the submicroscopic aspects of histiocytes as described in osseous, cutaneous, or pulmonary lesions of the histiocytosis X group. As yet undetermined cytoplasmic inclusion bodies constitute another rare observation in our material.

摘要

本文描述了一名23岁男性左足背侧所谓软组织巨细胞瘤病例的光镜和超微结构检查结果。患者接受了下肢截肢手术,随后接受了3个月的阿霉素化疗。尽管在首次切除时组织学和细胞学表现为恶性,且存在明显的血管侵犯,但2年后的最后已知情况似乎良好。腹股沟区无病理性淋巴结,胸部X线片无转移迹象。电镜研究未能就该肿瘤的组织发生得出明确结论。我们和其他人一样认为,许多主要的单核肿瘤细胞是低分化的间充质细胞。然而,一些肿瘤细胞显示出提示软骨母细胞或成骨细胞的超微结构特征(发育良好的粗面内质网含有电子致密物质;多个高尔基体复合体;大量糖原;相互交错的细胞膜绒毛;细胞质细丝;细胞外无定形基质)。一些较大的肿瘤细胞具有组织细胞增多症X组骨、皮肤或肺部病变中所描述的组织细胞亚微观特征。在我们的材料中,尚未确定的细胞质包涵体是另一罕见发现。

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