Llombart-Bosch A, Ortuño-Pacheco G
Histopathology. 1978 May;2(3):189-200. doi: 10.1111/j.1365-2559.1978.tb01709.x.
Electron microscopy of a case of adamantinoma of the tibia shows features which support a mesenchymal angioblastic origin rather than epithelial. Comparison is made between tissue from this tumour and a squamous cell carcinoma of the femur arising in chronic osteomyelitis. In adamantinoma no desmosomes are found between tumour cells and their cytoplasmic ultrastructure shows features of mesenchymal cell type including evidence of pinocytic activity and bundles of filaments resembling hyperplastic endothelial cells. The stroma shows features similar to fibrous dysplasia of bone with fibroblasts, histiocytes and fibrolipoblastic lipid-laden mesenchymal cells. It is condluded that adamantinoma of the tibia should be considered to be an angioblastic tumour of bone.
一例胫骨造釉细胞瘤的电子显微镜检查显示出的特征支持其间充质血管母细胞起源而非上皮起源。将该肿瘤组织与慢性骨髓炎中发生的股骨鳞状细胞癌组织进行了比较。在造釉细胞瘤中,肿瘤细胞之间未发现桥粒,其细胞质超微结构显示出间充质细胞类型的特征,包括有胞饮活性的证据以及类似于增生内皮细胞的丝状束。间质表现出与骨纤维异常增殖症相似的特征,有成纤维细胞、组织细胞和充满脂质的纤维脂肪母间充质细胞。结论是胫骨造釉细胞瘤应被视为一种骨血管母细胞瘤。