Malignant intestinal schwannoma. Case report.

Acta chirurgica Scandinavica Pub Date : 1990-10-01
D Hansen, A Pedersen, K M Pedersen
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引用次数: 0

Abstract

Malignant schwannoma of the small intestine is rare and diagnosis often late. Histologic distinction from fibrosarcoma and leiomyosarcoma may require electron microscopy. The primary treatment is surgical. Close postoperative observation is recommended because of the tendency to recurrence. Remission after chemotherapy has been reported, but without controlled studies. The 5-year survival rate is unknown. Two cases are presented.

恶性肠神经鞘瘤。病例报告。
小肠恶性神经鞘瘤是罕见的,诊断往往较晚。纤维肉瘤和平滑肌肉瘤的组织学区别可能需要电镜检查。主要的治疗方法是手术。由于有复发的倾向,建议术后密切观察。化疗后有缓解的报道,但没有对照研究。5年生存率未知。提出了两个案例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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