Destian S, Ritchie W G
Am J Gastroenterol. 1986 Aug;81(8):711-3.
Aggressive angiomyxoma is a rare benign tumor, arising in the pelvis usually presenting clinically as a perineal soft tissue mass displacing normal pelvic structures. The tumor is characterized by its locally aggressive nature and its tendency to recur after surgical resection. Although descriptions of this tumor have recently appeared in the pathology literature, to date, the radiological appearance of aggressive angiomyxoma has not been well documented. The CT scan in the following case report demonstrates the extent and location of the tumor, as well as its tendency to displace, rather than invade adjacent structures. These findings are consistent with the pathological characteristics of aggressive angiomyxoma, and therefore, can assist in its preoperative diagnosis.
侵袭性血管黏液瘤是一种罕见的良性肿瘤，通常发生于盆腔，临床上多表现为会阴软组织肿块，可推移正常盆腔结构。该肿瘤的特点是具有局部侵袭性，手术切除后有复发倾向。尽管近期病理学文献中已有关于此肿瘤的描述，但迄今为止，侵袭性血管黏液瘤的放射学表现尚未得到充分记录。以下病例报告中的CT扫描显示了肿瘤的范围和位置，以及其推移而非侵犯相邻结构的倾向。这些发现与侵袭性血管黏液瘤的病理特征相符，因此有助于其术前诊断。
