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subcutaneous pseudosarcomatous fibromatosis 皮下假肉瘤样纤维瘤病, 增生性筋膜炎
pseudosarcomatous fibromatosis 假性肉瘤性纤维瘤病
It was diagnosed as juvenile hyaline fibromatosis. 诊断:幼年透明蛋白纤维瘤病。
The differential diagnosis includes fibromatosis and chondroma of soft parts. 鉴别诊断包括纤维瘤病和软组织的软骨瘤。
In older patients, fibromatosis usually lacks calcification or chondroid differentiation. 对于老年患者，纤维瘤病通常缺少钙化或者软骨样分化。
Objective To evaluate CT imaging in the diagnosis of child glute al aggressive fibromatosis. 目的探讨ct对儿童臀部纤维瘤病的诊断价值。
Method:Three cases of aggressive fibromatosis of head and neck were analyzed retrospectively. 方法:回顾性分析3例头颈部侵袭性纤维瘤病患儿的临床资料。
Objective To introduce the experience on the diagnosis and treatment of desmoid fibromatosis. 目的介绍儿童臀部硬纤维瘤诊断及手术治疗的经验。
Objective:To investigate the value of MRI in the assessment of aggressive fibromatosis before operation. 目的:探讨MRI对侵袭性纤维瘤病术前评估的应用价值。
Objective:To discuss the therapy of aggressive fibromatosis of head and neck in children. 目的:探讨儿童头颈部侵袭性纤维瘤病的治疗方法。
Objective: To investigate the value of MRI in the assessment of aggressive fibromatosis before operation. 摘要目的：探讨MRI对侵袭性纤维瘤病术前评估的应用价值。
Objective:To explore the best treatment of aggressive fibromatosis tumor in jaw,face and Neck. 目的:探讨颌面颈部发生的侵袭性纤维瘤病的发病情况和治疗情况。
Fibromatosis and lymph nodes, both malignant and reactie, also need to be entertained in the differential diagnosis. 不论是恶性的还是反应性的纤维瘤病和淋巴结病变，在鉴别诊断时也需要考虑。
To summarize the diagnosis and treatment experience on aggressive fibromatosis in children. 总结小儿侵袭性纤维瘤病的诊治体会。
Aggressive fibromatosis (desmoid tumor) is a pathologic benign, uncommon, and often slowly growing fibrous tumor that is highly resistant to therapy. 摘要侵犯性纤维瘤病是一种良性、罕见、及时常缓慢生长的肿瘤，对于化学及放射线疗法常有抵抗性。
Methods 30 cases of desmoid fibromatosis were treated surgically,with complete resection for 22 cases and incomplete resection for 8 cases. 方法手术治疗儿童臀部硬纤维瘤30例，完整切除22例，次全切除8例。
Data of 19 cases with children aggressive fibromatosis admitted between Jan. 1990 and Mar. 2004 were retrospectively reviewed. 对1990年1月至2004年3月治疗的19例小儿侵袭性纤维瘤病资料进行回顾性分析。
In infants, fibromatosis usually involves the head, neck and proximal extremities, the background is more myxoid than chondroid, and calcification is rare. 在婴儿，纤维瘤病经常累及头部、颈部和邻近的四肢，背景以粘液为主，少量的软骨样间质，钙化罕见。
Methods: Polymerase chain reaction-single strand conformation polymorphism(PCR-SSCP) was used to exclude known gene mutation of HGF from 2 familial gingival fibromatosis. 方法：采用PCR-SSCP-银染的方法对2例遗传性牙龈纤维瘤病家系的致病基因进行排除性定位。
Conclusion: MRI can demonstrate the histiologic features of aggressive fibromatosis and involvement of vessles, and can be choosed as the primary method for diagnosis. 结论:侵袭性纤维瘤病的MRI表现具有一定特征性，MRI可反映侵袭性纤维瘤病的组织学特点，并能显示肿瘤与邻近血管的关系，可作为诊断侵袭性纤维瘤病的首选方法。