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髂腰肌间隙原发性恶性肿瘤。

Primary malignant tumors of the iliopsoas compartment.

作者信息

Behranwala Kasim A, A'Hern Roger, Thomas J Meirion

机构信息

Sarcoma and Melanoma Unit (Academic Surgery), Royal Marsden NHS Trust, United Kingdom.

出版信息

J Surg Oncol. 2004 May 1;86(2):78-83. doi: 10.1002/jso.20047.

Abstract

BACKGROUND AND OBJECTIVES

Primary malignant tumors of the iliopsoas compartment are rare entities that have been infrequently reported. We present our experience of iliopsoas malignancy to better characterize and define the natural history of this condition.

METHODS

Primary iliopsoas tumors occurring from January 1990 were identified from the Royal Marsden Hospital's (RMH) Sarcoma Unit prospective database.

RESULTS

Nineteen malignant tumors (11 limited to the psoas muscle only, 1 involving only the iliacus muscle and 7 involving both the iliacus and psoas) of the iliopsoas compartment were evaluated and treated at the RMH during this period. Leiomyosarcoma (n = 5) and liposarcoma (n = 3) were the most frequent histologic types. There were 3 G1, 5 G2, 10 G3 tumors and grade could not be assessed in 1 patient. There were 17 T2 tumors and size was not available in 2 patients. Surgery was done in 14 patients (negative microscopic margins-7, positive microscopic margins-3, and positive gross margins-3 and the margin of excision was not known in 1 patient). Five of 14 surgically treated patients had local recurrence and 6 of 19 patients developed metastases. Ten patients died of their disease at a median follow-up of 12 months. The estimated 2 and 5 year survival rates were 44 and 23%, respectively.

CONCLUSIONS

Tumors in this location have a poor prognosis due to the lack of early diagnosis, large size at presentation, multiple attachments of the psoas muscle, and being relatively surgically inaccessible.

摘要

背景与目的

髂腰肌间隙原发性恶性肿瘤是罕见的实体,报道较少。我们介绍我们在髂腰肌恶性肿瘤方面的经验,以更好地描述和界定这种疾病的自然病程。

方法

从皇家马斯登医院(RMH)肉瘤科前瞻性数据库中识别出1990年1月以来发生的原发性髂腰肌肿瘤。

结果

在此期间,RMH对19例髂腰肌间隙恶性肿瘤(11例仅局限于腰大肌,1例仅累及髂肌,7例同时累及髂肌和腰大肌)进行了评估和治疗。平滑肌肉瘤(n = 5)和脂肪肉瘤(n = 3)是最常见的组织学类型。有3例G1级、5例G2级、10例G3级肿瘤,1例患者分级无法评估。有17例T2期肿瘤,2例患者肿瘤大小未知。14例患者接受了手术(显微镜下切缘阴性-7例,显微镜下切缘阳性-3例,大体切缘阳性-3例,1例患者切除切缘情况未知)。14例接受手术治疗的患者中有5例出现局部复发,19例患者中有6例发生转移。10例患者在中位随访12个月时死于疾病。估计2年和5年生存率分别为44%和

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