Metastatic chordoma use of mechlorethamine (nitrogen mustard) in chordoma therapy.

A. McSweeney, P. Sholl
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引用次数: 17

Abstract

The sacrococcygeal chordoma is a rare tumor which is generally believed to arise from remnants of embryonic notochordal tissues. These may persist as the nucleus pulposus or in scattered nodular rests in some 2% of humans.1A recent review of the literature revealed a total of 505 cases of chordoma.2Chordomas show a predilection for the sacrum and coccyx, and about half are located in these areas. Although chordomas are malignant tumors in every sense and are locally invasive, proved metastases are very uncommon. Apparently, metastases from mucus-producing carcinomas of the rectum have in some cases been confused with metastatic chordoma. We are aware of only one case of presumable distant bony metastasis of a chordoma, but this was not proved by histologic examination.3 The primary therapeutic approach to sacrococcygeal chordomas is surgical. Block removal of the coccyx, most of the sacrum, and the tumor is recommended
转移性脊索瘤氯胺(氮芥)在脊索瘤治疗中的应用。
骶尾脊索瘤是一种罕见的肿瘤,一般认为起源于胚胎脊索组织的残余。在大约2%的人中,这些可能持续存在于髓核或分散的结节性休息中。最近的文献回顾显示,共有505例脊索瘤。脊索瘤多发于骶骨和尾骨,约一半位于这些部位。虽然脊索瘤在任何意义上都是恶性肿瘤,并且是局部侵袭性的,但证实转移是非常罕见的。显然,从直肠产生黏液的癌转移在某些情况下与转移脊索瘤混淆。我们只知道一例脊索瘤可能发生远端骨转移,但这并没有得到组织学检查的证实骶尾脊索瘤的主要治疗方法是手术。建议切除尾骨、大部分骶骨和肿瘤
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