Suppr超能文献

[软组织硬纤维瘤病的影像学表现及病理特征]

[Imaging manifestations and pathologic features of soft tissue desmoid-type fibromatosis].

作者信息

Liu Qing-Yu, Chen Jian-Yu, Liang Bi-Ling, Li Hai-Gang, Gao Ming, Lin Xiao-Feng

机构信息

Department of Radiology, The Second Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, 510120, PR China.

出版信息

Ai Zheng. 2008 Dec;27(12):1287-92.

Abstract

BACKGROUND & OBJECTIVE: Soft tissue desmoid-type fibromatosis is a type of benign, infiltrative tumors which are rarely seen. This study was to analyze CT and MR manifestations and pathologic features of soft tissue desmoid-type fibromatosis to improve its diagnostic accuracy.

METHODS

A total of 34 soft tissue desmoid-type fibromatosis from 29 patients, including 20 primary and 14 recurrent tumors were analyzed. Eight were scanned with CT, and 26 were scanned with MRI. Features of the growth pattern, CT or MRI findings and pathologic appearances of the tumors were studied.

RESULTS

The mean size of the 34 tumors was 6.5 cm. Of the 34 tumors, 31(91.2%) had an ill-defined or partially ill-defined margin, 31(91.2%) had a lobulated or irregular contour, 17(50.0%) had neurovascular involvement, 15(44.1%) had bone involvement, 23(67.6%) had extra-compartmental extension. Among the eight tumors scanned by CT, six showed slight hypodensity on the non-enhanced CT scan, and seven were inhomogeneously enhanced after contrast injection. Twenty-six tumors scanned by MRI appeared either iso-or slightly hyperintense on T1W images, hyperintense on T2W images, and moderate or intense enhancement after gadolinium administration. Heterogeneous signal intensity was detected in 88.5%(23/26) tumors. Linear and curvilinear areas of signal void interspersed throughout the tumors were found in 22 tumors(84.6%) on both T1W and T2W images. Histologic analysis revealed that the tumor was composed of spindle cells and collagen bundles, with a variable amount of intermingled collagen surrounding the spindle cells. Nuclear atypia was not seen,and occasional mitoses were present in the tumor cells.

CONCLUSION

The characteristic manifestations of CT or MR images of desmoid-type fibromatosis provide important evidence to discriminate benign and malignant soft tissue tumors.

摘要

背景与目的

软组织硬纤维瘤病是一种少见的良性浸润性肿瘤。本研究旨在分析软组织硬纤维瘤病的CT和MR表现及病理特征,以提高其诊断准确性。

方法

分析29例患者的34个软组织硬纤维瘤病,其中包括20个原发肿瘤和14个复发肿瘤。8例行CT扫描,26例行MRI扫描。研究肿瘤的生长方式、CT或MRI表现及病理特征。

结果

34个肿瘤的平均大小为6.5 cm。34个肿瘤中,31个(91.2%)边界不清或部分边界不清,31个(91.2%)轮廓呈分叶状或不规则,17个(50.0%)有神经血管受累,15个(44.1%)有骨质受累,23个(67.6%)有跨肌间隙扩展。8个CT扫描的肿瘤中,6个在平扫CT上呈轻度低密度,7个增强后呈不均匀强化。26个MRI扫描的肿瘤在T1WI上呈等信号或稍高信号,T2WI上呈高信号,钆剂注射后呈中度或明显强化。88.5%(23/26)的肿瘤信号强度不均匀。在T1WI和T2WI上,22个肿瘤(84.6%)可见线性和曲线状无信号区散在分布于肿瘤内。组织学分析显示,肿瘤由梭形细胞和胶原束组成,梭形细胞周围有不同量的交织胶原。未见核异型性,肿瘤细胞可见偶尔的核分裂象。

结论

硬纤维瘤病的CT或MR特征性表现为鉴别良恶性软组织肿瘤提供了重要依据。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验