复发性脊索瘤引起的恶性纤维组织细胞瘤。病例报告及电镜检查结果。

M Makek, H J Leu
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引用次数: 8

摘要

我们提出的病例骶尾脊索瘤复发后15年的根治作为一个软组织肿瘤在臀肌组织。该肿瘤由两部分组成:无侵袭性细胞增殖症状的脊索瘤和恶性纤维组织细胞瘤。在接下来的4年里,在臀部肌肉组织中发生了几次恶性纤维组织细胞瘤的局部复发。患者最终死于肺转移。肺、臀肌及骶尾骨区未见脊索瘤肿瘤组织。组织学包括电子显微镜显示没有证据表明脊索瘤转变为恶性纤维组织细胞瘤。必须假设继发性软组织肿瘤起源于原发肿瘤手术期间植入的残余脊索瘤细胞。恶性纤维组织细胞瘤是起源于脊索瘤内的间充质间质细胞,还是直接起源于原始神经外胚层脊索细胞,后者具有分化为多种细胞类型的能力,包括间充质细胞,目前尚不清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Malignant fibrous histiocytoma arising in a recurrent chordoma. Case report and electron microscopic findings.

We present the case of a sacrococcygeal chordoma which recurred 15 years after the radical removal as a soft tissue tumor in the gluteal musculature. This tumor consisted of two parts: a chordoma without symptoms of aggressive cellular proliferation and a malignant fibrous histiocytoma. During the following 4 years several local recurrences of the malignant fibrous histiocytoma occurred in the gluteal musculature. The patient finally died of lung metastases. No chordoma tumor tissue was found in the lungs, in the gluteal musculature or in the sacrococcygeal bone area. Histology including electron microscopy revealed no proof of a transition of chordoma into malignant fibrous histiocytoma. It must be assumed that the secondary soft tissue tumor originated from residual chordoma cells which were implanted during the operation of the primary tumor. It remains unclear whether the malignant fibrous histiocytoma arose from mesenchymal stromal cells within the chordoma or directly from primitive neuroectodermal chorda cells which possess the ability to differentiate into a variety of cell types including mesenchymal cells.

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