...
首页> 外文期刊>Radiographics >From the archives of the AFIP: musculoskeletal fibromatoses: radiologic-pathologic correlation.
【24h】

From the archives of the AFIP: musculoskeletal fibromatoses: radiologic-pathologic correlation.

机译:来自AFIP的档案:肌肉骨骼纤维瘤:放射病理相关性。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Musculoskeletal fibromatoses represent a wide spectrum of fibroblastic and myofibroblastic neoplasms with similar pathologic appearances and variable clinical behavior. These lesions can be categorized by location (superficial or deep) or by the age group predominantly affected. Superficial fibromatoses in adults (palmar and plantar) and children (calcifying aponeurotic fibroma, lipofibromatosis, and inclusion body fibromatosis) are often small slow-growing lesions; their diagnosis is suggested by location. Deep fibromatoses in adults (desmoid type and abdominal wall) and children (fibromatosis colli and myofibroma and myofibromatosis) are frequently large and more rapidly enlarging; location of these lesions may be nonspecific. Radiographic findings typically are nonspecific. Cross-sectional imaging (ultrasonography, computed tomography, or magnetic resonance [MR] imaging) reveals lesion location, extent, and involvement of adjacent structures for staging and evaluation of local recurrence. MR imaging findings of predominantly low to intermediate signal intensity, nonenhancing bands of low signal intensity on long repetition time MR images that represent collagenized regions, and extension along fascial planes ("fascial tail" sign) add specificity for diagnosis. Additional features that aid in diagnostic specificity include an abdominal wall location related to pregnancy (abdominal wall fibromatosis), a lower neck location in a young child (fibromatosis colli), an adipose component (lipofibromatosis), or multiple lesions in young children (myofibromatosis). Treatment may be conservative or surgical resection, depending on the specific diagnosis. Local recurrence is common after surgical resection owing to the infiltrative growth of these lesions. Recognition that the appearances of the various types of musculoskeletal fibromatoses reflect their pathologic characteristics improves radiologic assessment and helps optimize patient management.
机译:肌肉骨骼肌纤维瘤代表着广泛的成纤维细胞和肌成纤维细胞肿瘤,具有相似的病理学表现和可变的临床行为。这些病变可按部位(浅表或深部)或主要受影响的年龄组分类。成人(颅骨和足底)和儿童(钙化性腱膜纤维瘤,脂肪纤维瘤病和包涵体纤维瘤病)的浅表纤维瘤通常是缓慢生长的小病变;根据位置建议诊断。成人(类胶体型和腹壁)和儿童(纤维状结肠病,肌纤维瘤和肌纤维瘤病)的深部纤维瘤往往很大,并且迅速增大。这些病变的位置可能是非特异性的。射线照相结果通常是非特异性的。横断面成像(超声检查,计算机断层扫描或磁共振成像[MR]成像)显示病变的位置,程度和邻近结构的累及,以进行分期和评估局部复发。 MR成像发现主要是中低信号强度,在较长的重复时间MR图像(代表胶原蛋白区域)上沿信号强度的非增强带,以及沿筋膜平面延伸(“筋膜尾巴”征)增加了诊断的特异性。有助于诊断特异性的其他功能包括与妊娠相关的腹壁位置(腹壁纤维瘤病),幼儿的下颈部位置(纤维瘤病柯利),脂肪成分(脂纤维瘤病)或幼儿的多处病变(肌纤维瘤病) 。根据具体的诊断,可以采用保守或手术切除的治疗方法。由于这些病灶的浸润性增长,手术切除后局部复发是常见的。认识到各种类型的肌肉骨骼肌纤维瘤的出现反映了它们的病理特征,可以改善放射学评估并有助于优化患者管理。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号