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Case report 235. Ewing-like adamantinoma of the left radial head and neck.

作者信息

Lipper S, Kahn L B

出版信息

Skeletal Radiol. 1983;10(1):61-6. doi: 10.1007/BF00355396.

DOI:10.1007/BF00355396
PMID:6879221
Abstract

Skeletal adamantinoma is a rare malignant bone tumor with a poorly understood histogenesis. The lesion is easily recognized by a distinctive microscopic pattern of anastomosing trabeculae of epithelial-like cells in a fibrous stroma. Ultrastructural evidence has been presented to support an origin from two widely-divergent cell types: an epithelial cell with squamous characteristics [12, 15] and a mesenchymal cell with endothelial features [5, 9]. An addition to the histogenetic controversy has been the recent description of a bone neoplasm with an adamantinoma-like growth pattern which proved both by subsequent histological evolution and ultrastructure, to have features of Ewing tumor [10]. The authors report a further example of this entity and suggest that it may be sufficiently distinctive within the adamantinoma group to merit the term Ewing-like adamantinoma. Consonant with increasing evidence supporting the concept of tumor "metaplasia" that transcends traditional concepts of epithelial-mesenchymal immutability, the authors propose that all adamantinomas arise from a common stem cell.

摘要

相似文献

1
Case report 235. Ewing-like adamantinoma of the left radial head and neck.
Skeletal Radiol. 1983;10(1):61-6. doi: 10.1007/BF00355396.
2
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5
Morphologic diversity of long bone adamantinoma. The concept of differentiated (regressing) adamantinoma and its relationship to osteofibrous dysplasia.长骨造釉细胞瘤的形态学多样性。分化型(消退型)造釉细胞瘤的概念及其与骨纤维发育不良的关系。
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[Classic adamantinoma, differentiated adamantinoma and osteofibrous dysplasia of long bones].[经典型造釉细胞瘤、分化型造釉细胞瘤及长骨骨纤维结构不良]
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Pathol Res Pract. 1979 Dec;166(1):112-22. doi: 10.1016/S0344-0338(79)80012-6.

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本文引用的文献

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Adamantinoma of the tibia. Electron microscopic evidence of its epithelial origin.胫骨造釉细胞瘤。其上皮起源的电镜证据。
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Adamantinoma-like Ewing's sarcoma with EWS-FLI1 fusion gene: a case report.伴有EWS-FLI1融合基因的成釉细胞瘤样尤因肉瘤:一例报告
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Adamantinoma, osteofibrous dysplasia and differentiated adamantinoma.造釉细胞瘤、骨纤维发育不良和分化型造釉细胞瘤。
Skeletal Radiol. 2003 May;32(5):245-58. doi: 10.1007/s00256-003-0624-2. Epub 2003 Mar 22.
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Ewing's sarcoma of humerus with epithelial differentiation.伴有上皮分化的肱骨尤因肉瘤
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9
Case report 727. Juxtacortical adamantinoma of humerus (simulating Ewing tumor).病例报告727。肱骨皮质旁造釉细胞瘤(酷似尤因肉瘤)。
Skeletal Radiol. 1992;21(3):205-9. doi: 10.1007/BF00242139.
10
A clinicopathological and immunohistochemical study of osteofibrous dysplasia, differentiated adamantinoma, and adamantinoma of long bones.骨纤维结构不良、分化型造釉细胞瘤及长骨造釉细胞瘤的临床病理及免疫组化研究
Skeletal Radiol. 1992;21(8):493-502. doi: 10.1007/BF00195230.
[Mixed-cell sarcoma].[混合细胞肉瘤]
Verh Dtsch Ges Pathol. 1974;58:265-70.
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Adamantinomas of long bones.
Cancer. 1974 Nov;34(5):1796-805. doi: 10.1002/1097-0142(197411)34:5<1796::aid-cncr2820340530>3.0.co;2-z.
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Spindle cell carcinoma: ultrastructural evidence of squamous origin and collagen production by the tumor cells.梭形细胞癌:肿瘤细胞鳞状起源及产生胶原蛋白的超微结构证据。
Cancer. 1976 May;37(5):2275-82. doi: 10.1002/1097-0142(197605)37:5<2275::aid-cncr2820370518>3.0.co;2-3.
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Adamantinoma of long bones. A clinicopathological study of fourteen cases with vascular origin suggested.长骨造釉细胞瘤。14例提示血管起源的临床病理研究。
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A perplexing malignant bone tumor. Highly malignant so-called adamantinoma or non-typical Ewing's sarcoma.一种令人困惑的恶性骨肿瘤。高恶性的所谓造釉细胞瘤或非典型尤因肉瘤。
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Ultrastructural findings supporting the angioblastic nature of the so-called adamantinoma of the tibia.超微结构研究结果支持所谓胫骨成釉细胞瘤的血管母细胞性质。
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