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胃平滑肌肉瘤:自然病史、预后因素及治疗

Myosarcomas of the stomach: natural history, prognostic factors and management.

作者信息

Shiu M H, Farr G H, Papachristou D N, Hajdu S I

出版信息

Cancer. 1982 Jan 1;49(1):177-87. doi: 10.1002/1097-0142(19820101)49:1<177::aid-cncr2820490136>3.0.co;2-k.

Abstract

A retrospective study was made of 41 patients treated for gastric myosarcoma to identify prognostic factors that influence results. The adjusted five- and ten-year survival rates were 56% and 43% respectively, with no significant difference between leiomyosarcoma and malignant leiomyoblastoma. A histopathologic grade of malignancy could be assigned to each tumor according to the degree of hypercellularity, nuclear abnormality, mitotic rate and other characteristics. High histopathologic grade, large tumor size (greater than 5 cm diameter) and invasion of adjacent organs adversely affected prognosis. Five-year survival after curative treatment was: 100% (9/9) for small tumors, of which six were treated by wedge gastric resection; 67% (8/12) for large tumors, mostly after subtotal gastrectomy; and 0% for tumors that invaded adjacent organs, despite extended resections. It is concluded that the management of gastric myosarcomas can be planned according to these prognostic factors and that multimodal therapy of tumors with adverse factors warrants consideration.

摘要

对41例接受胃平滑肌肉瘤治疗的患者进行了回顾性研究,以确定影响治疗结果的预后因素。调整后的5年和10年生存率分别为56%和43%,平滑肌肉瘤与恶性平滑肌瘤病之间无显著差异。根据细胞增多程度、核异常、有丝分裂率和其他特征,可为每个肿瘤指定组织病理学恶性等级。高组织病理学分级、肿瘤体积大(直径大于5cm)和侵犯相邻器官对预后有不利影响。根治性治疗后的5年生存率为:小肿瘤为100%(9/9),其中6例采用楔形胃切除术治疗;大肿瘤为67%(8/12),大多在胃次全切除术后;侵犯相邻器官的肿瘤,尽管进行了扩大切除,生存率为0%。结论是,可根据这些预后因素规划胃平滑肌肉瘤的治疗,对于具有不利因素的肿瘤,多模式治疗值得考虑。

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