股骨软骨肉瘤与肿瘤生长的组织学影像学相关性——关于骨膜新骨形成和软组织延伸的初步观察。

German C Steiner, Mark E Schweitzer, Samuel Kenan, Ibrahim F Abdelwahab
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引用次数: 0

摘要

未标记:本研究的目的是,在股骨软骨肉瘤(CHS)中,通过影像学和病理学的相关性来评估肿瘤生长、皮质破坏、骨膜反应和软组织延伸的程度。材料与方法:对8例经组织学证实的股骨CHS进行了研究。所有病例均被切除,用冠状板进行组织学评估,并与x线片和磁共振成像(MRI)扫描进行比较。在两个切除的标本中,对肿瘤进行了更详细的研究;除冠状面片外,对两个肿瘤剩余的前后半部分进行轴向切片,并对骨标本进行x光和组织学检查。结果:CHS最初累及髓腔,随后破坏皮层;首先是内层扇贝作用,其次是随后对皮层的侵袭和破坏。在此过程中,有骨膜新骨形成(PNBF),皮质厚度增加,其程度往往与皮质破坏程度相关。在3例皮质增厚的区域,MRI上看到一条“灰线”,将皮质与骨膜新生骨分开;实际上,这条线是两个结构之间的空间。这条线的存在表明肿瘤没有扩展到皮层以外。所有病例均出现PNBF,且厚度不同。它经常独立于骨膜肿瘤的直接累及而发展。1例骨膜含骨质疏松伴骨髓脂肪浸润,MRI易误诊为肿瘤扩展。CHS的股骨干扩张和重塑,伴髓腔变宽,通常是由于PNBF广泛的皮质破坏所致。5例患者出现软组织扩张,明显有两种不同的机制:肿瘤直接破坏皮层和骨膜,并扩展到软组织;MRI表现为隐蔽性肿瘤穿透骨膜。据我们所知,第一个文献组织学描述增厚CHS骨膜也完成。结论:PNBF是股骨CHS的常见影像学表现,与皮质破坏程度相关。皮层和骨膜之间的灰线是本研究描述的MRI发现,可能有助于评估CHS骨膜增厚和肿瘤侵袭。PNBF通常发生在没有直接累及骨膜的情况下。提示肿瘤浸润的骨膜成像异常在MRI上应谨慎解释,CHS的早期软组织扩张可能难以在MRI上确定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chondrosarcoma of the femur with histology-imaging correlation of tumor growth--preliminary observations concerning periosteal new bone formation and soft tissue extension.

Unlabelled: The objective of this study was, in chondrosarcoma (CHS) of the femur, to evaluate by radiologic-pathologic correlation, the degree of tumor growth, cortical destruction, periosteal reaction, and soft tissue extension present.

Materials and methods: Eight cases of histologically proven CHS of the femur were studied. All cases were resected, evaluated histologically with coronal slabs, and compared with radiographs and magnetic resonance imaging (MRI) scans. In two resected specimens, the tumors were studied in more detail; along with coronal slabs, axial sections of the remaining anterior and posterior halves of both tumors were taken, and the bone specimens were X-rayed and examined histologically.

Results: CHS initially involved the medullary cavity and subsequently destroyed the cortex; first, by endosteal scalloping and, second, by subsequent invasion and destruction of the cortex. During this process, there was periosteal new bone formation (PNBF), with increased cortical thickness, the degree of which often correlated with the degree of cortical destruction. In the areas of cortical thickening of three cases, a "grey line" was seen on MRI that separated the cortex from the periosteal new bone; the line, in reality,is a space between the two structures. The presence of this line suggests that the tumor does not extend beyond the cortex. PNBF occurred in all cases and varied in thickness. It frequently developed independent of direct periosteal tumor involvement. The periosteum of one case contained porotic bone with interposed marrow fat, which was easily misinterpreted as tumor extension on MRI. Expansion and remodeling of the femoral diaphysis in CHS, with widening of the medullary cavity, is usually due to extensive cortical destruction with PNBF. Soft tissue extension was present in five cases and apparently occurred by two different mechanisms: direct tumor destruction of the cortex and periosteum, with extension into the soft tissues; and subtle MRI occult tumor permeation through the periosteum. As far as we know, a first literature histologic description of the thickened CHS periosteum also was accomplished.

Conclusion: PNBF is a common imaging manifestation of CHS of the femur, which correlated with the degree of cortical destruction. A grey line between the cortex and periosteum is an MRI finding described in this study and may facilitate the evaluation of periosteal thickening and tumor invasion in CHS. PNBF often occurs in the absence of direct periosteal involvement. Periosteal imaging abnormalities suggestive of tumor infiltration should be interpreted with caution on MRI, and early soft tissue extension in CHS may be difficult to determine on MRI.

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