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骨巨细胞瘤的本质。

The nature of giant cell tumor of bone.

作者信息

Wülling M, Engels C, Jesse N, Werner M, Delling G, Kaiser E

机构信息

Department of Osteopathology/Center of Biomechanics, University-Hospital Hamburg-Eppendorf, Hamburg, Germany.

出版信息

J Cancer Res Clin Oncol. 2001 Aug;127(8):467-74. doi: 10.1007/s004320100234.

Abstract

Giant cell tumor of bone (GCT) is a locally osteolytic tumor with variable aggressiveness. In rare cases, pulmonary metastasis can be observed. The lesion most frequently occurs in the epiphysis of long tubular bones of the knee region, predominantly affecting young adults after closure of the growth plate. The characteristic histological appearance of GCT displays a high number of osteoclast-like multinucleated giant cells, which resulted in the classification "osteoclastoma" or "giant cell tumor". Apart from the multinucleated giant cells, there are two mononuclear cell types in GCT. The first one has a round morphology and resembles monocytes. The second cell type is the spindle-shaped, fibroblast-like stromal cell. Cell culture experiments with GCT cells revealed the stromal cell to be the proliferating component of the GCT. The other two cell types, the monocyte and the multinucleated giant cell, were lost after a few cell culture passages. Furthermore, latest results from GCT reveal that the stromal cells secrete a variety of cytokines and differentiation factors, including MCP1, ODF, and M-CSF. These molecules are monocyte chemoattractants and are essential for osteoclast differentiation, suggesting that the stromal cell stimulates blood monocyte immigration into tumor tissue and enhances their fusion into osteoclast-like, multinucleated giant cells. The multinucleated giant cell itself resembles a normal osteoclast that is able to resorb bone leading to extended osteolysis. This new model of GCT genesis supports the hypothesis that the stromal cell is the neoplastic component whilst the monocytes and the multinucleated giant cells are just reactive components of this tumor. Taking this into consideration, the nomenclature of the "giant cell tumor" needs to be reconsidered.

摘要

骨巨细胞瘤(GCT)是一种具有不同侵袭性的局部溶骨性肿瘤。在罕见情况下,可观察到肺转移。该病变最常发生在膝关节区域长管状骨的骨骺,主要影响生长板闭合后的年轻成年人。GCT的特征性组织学表现为大量破骨细胞样多核巨细胞,这导致了“破骨细胞瘤”或“巨细胞瘤”的分类。除了多核巨细胞外,GCT中有两种单核细胞类型。第一种呈圆形,类似于单核细胞。第二种细胞类型是梭形的、成纤维细胞样的基质细胞。对GCT细胞进行的细胞培养实验表明,基质细胞是GCT的增殖成分。另外两种细胞类型,即单核细胞和多核巨细胞,在几次细胞培养传代后消失。此外,GCT的最新研究结果表明,基质细胞分泌多种细胞因子和分化因子,包括MCP1、ODF和M-CSF。这些分子是单核细胞趋化剂,对破骨细胞分化至关重要,这表明基质细胞刺激血液单核细胞迁移到肿瘤组织中,并增强它们融合成破骨细胞样的多核巨细胞。多核巨细胞本身类似于正常的破骨细胞,能够吸收骨质,导致广泛的骨质溶解。这种新的GCT发生模型支持这样一种假说,即基质细胞是肿瘤成分,而单核细胞和多核巨细胞只是该肿瘤的反应性成分。考虑到这一点,“巨细胞瘤”的命名需要重新考虑。

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