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作 者:付芳芳[1] 史大鹏[1] 陈翠云[1] 刘冬[2] 沈海林[2]
机构地区:[1]河南省人民医院放射科,河南郑州450003 [2]苏州大学第一附属医院影像科
出 处:《实用放射学杂志》2012年第10期1591-1594,共4页Journal of Practical Radiology
摘 要:目的探讨韧带样型纤维瘤病(desmoids—typefibromatosis,DF)的多层螺旋CT(MSCT)和MRI表现,以期提高对该病的认识。方法回顾性分析经手术病理证实的13例DF患者的临床及影像资料。结果13例DF中腹外型9例,腹壁型4例。肿块最大径平均为8.8cm(范围1.8~15.0cm),呈椭圆形或不规则形,无包膜,边界与周围组织分界不清,瘤内囊变、出血、坏死少见,均未见灶周水肿。6例行CT平扫和增强检查,平扫示肿块密度均匀,与肌肉密度相近,增强后呈轻、中度强化。8例行MRI平扫,之后其中6例行增强扫描,平扫示T1WI序列6例呈等信号,2例呈稍高信号,T2WI及STIR序列均呈高信号,信号不均匀,其内均可见斑点状或条带状低信号区,其中5例肿块内可见流空血管影;增强后病灶呈明显不均匀强化。结论DF是一种罕见的软组织肿瘤,其MSCT、MRI表现具有一定特征性,可为临床诊断提供客观依据,但确诊依赖病理。Objective To review MSCT and MRI findings of desmoid-type fibromatosis (DF). Methods The clinic data, and MSCT and MRI findings of 13 pathologically proved cases of DF were retrospectively analyzed. Results Lesions were in extra ab- dominal location in 9 cases, and in abdominal wall muscles in 4 cases. The average size was 8.8 cm (range, 1.8--15.0 cm), oval or irregular, with no capsule or clear boundary. There were few cystic, hemorrhagic and necrotic areas within the tumors, and there was no peri-lesion edema. Plain and contrast-enhanced CT was performed before operation in 6 cases. The masses were homogene- ous and of similar densities to the muscles on CT plain scan, and showed mild or moderate enhancement. 8 patients underwent MR examination (6 of which contrast-enhancement). The masses showed iso-intensity in 6 cases and mild hypevintensity in 2 cases on T1WI, and hyper-intensity in all 8 cases on T2WI or STIR images. Spots or linear areas of low signal intensity were detected within tumors on all the MR images. Vascular flow void phenomenon was seen in 5 cases. All lesions showed intense enhancement on con- trast-enhanced MR. Conclusion DF is a rare soft tissue tumor, and is often clinically misdiagnosed. MSCT and MRI show certain imaging features, and could provide an objective basis for clinical diagnosis.
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