介绍
计算机科学
奇纳
肉瘤
软组织
软组织肉瘤
不错
梅德林
癌症
观察研究
医学
病理
普通外科
外科
家庭医学
内科学
护理部
程序设计语言
法学
心理干预
政治学
作者
Shiba Sinha,A.H.S. Peach
出处
期刊:BMJ
[BMJ]
日期:2010-12-29
卷期号:341 (dec29 1): c7170-c7170
被引量:69
摘要
#### Summary points
Soft tissue sarcomas are a heterogeneous group of tumours of mesodermal origin. Although they are rare, accounting for less than 1% of all malignant tumours, half of patients diagnosed will die from the sarcoma.1 w1 Lumps are commonly encountered in primary and specialist care, and differentiating benign from possibly malignant lesions can be difficult. The estimated benign:malignant ratio is 100:1. A family doctor will see about one case of soft tissue sarcoma for every 24 years of practice.w2 However, prognosis is related to size at presentation, so early recognition, referral to a specialist (see National Institute for Health and Clinical Excellence (NICE) guidelines), and appropriate treatment improve outcomes.2 Evidence from cohort studies suggests that patients experience delays in referral,w3 w4 and in the United Kingdom referrals to specialist sarcoma centres often fall outside the recommended two week window for suspected cancer.3 4 We review evidence from national guidelines, randomised trials, and observational studies to provide the non-specialist with a guide to diagnosis, appropriate referral, and management of patients with suspected soft tissue sarcoma, focusing on a multidisciplinary approach. We limit our discussion of management to the treatment of soft tissue sarcoma of the extremities—the most common site.
#### Sources and selection criteria
We searched Medline, PubMed, Embase, and CINAHL using the terms “soft …
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