罕见的原发性脊髓间充质软骨肉瘤1例报告

Sushil Paudel, Shirish Adhikari, Sharad C Adhikari, Rohit K Pokharel
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引用次数: 0

摘要

原发性硬膜外间充质软骨肉瘤是一种非常罕见的椎管内肿瘤。通过磁共振成像(MRI)和活检肿块进行适当的临床评估可以确认诊断。由于MCS有很高的复发和转移趋势,因此预后受到保护。我们报告一名52岁男性,腰骶部(L5-S3)原发性硬膜外MCS。进行了部分切除和活检,证实了诊断。患者接受了切除后的放射治疗,但在四个月后过期。尽管这种肿瘤很罕见,但应该保持差异,这有助于早期诊断,因此可以通过彻底切除肿块和术后放疗进行治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rare Primary Spinal Mesenchymal Chondrosarcoma: A Case Report
Primary extradural mesenchymal chondrosarcoma (MCS) is a very rare intraspinal tumor. Proper clinical evaluation with magnetic resonance imaging (MRI) followed by biopsy of the mass can confirm the diagnosis. Since MCS has a high tendency of recurrence and metastasis, the prognosis is guarded. We report a 52 years old male with primary extradural MCS in the lumbosacral region (L5-S3). Subtotal excision and biopsy were performed which confirmed the diagnosis. The patient received post excisional radiotherapy but expired after four months. Though rare, this tumor should be kept in differentials which helps in early diagnosis and thus can be treated with radical excision of the mass along with postoperative radiotherapy.
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