Heaton J M, Turner D R
Histopathology. 1985 May;9(5):543-50. doi: 10.1111/j.1365-2559.1985.tb02835.x.
This study of thirteen cases of chordoma serves to emphasize the occurrence of three different histological patterns; classical, seven; chondroid, three; and intermediate or mesenchymal, three. The study also suggests that more adequate sampling of these tumours detects the chondroid variant more readily. These varying patterns of differentiation in tumours of notochordal origin suggest that the parent tissue may have the potential to develop along similar lines in the embryo. Thus mesenchymal and cartilaginous tissue formed from notochordal cells could contribute to the formation of the nucleus pulposus and inner portion of the intervertebral disc cartilages. This concept contrasts with the previously held view that the notochord atrophies at an early stage in embryonic development.
这项对13例脊索瘤病例的研究旨在强调三种不同组织学模式的出现情况:经典型,7例;软骨样型,3例;中间型或间充质型,3例。该研究还表明,对这些肿瘤进行更充分的取样能更容易地检测到软骨样变体。脊索瘤起源肿瘤的这些不同分化模式表明,其母组织在胚胎中可能有沿着相似路径发育的潜力。因此,由脊索细胞形成的间充质和软骨组织可能有助于髓核和椎间盘软骨内部的形成。这一概念与之前认为脊索在胚胎发育早期萎缩的观点形成对比。