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Objective： To evaluate the clinical feature and treatment of desmoid tumor. 目的：探讨硬纤维瘤的临床特点和治疗方法。
Objective To evaluate the clinical feature and treatment of abdominal wall desmoid tumor. 目的探讨腹壁韧带样纤维瘤的临床特点和治疗;
Figure 16. A, Desmoid tumor in a previous scar. B, Color Doppler scan of a Desmoid tumor in a previous scar revealing some vascularity in the lesion. 图16，A，以前疤痕处的硬纤维瘤。B，彩色多普勒扫描以前瘢痕处的硬纤维瘤病变处显示一些血管供应。
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。
Figure 16. A, Desmoid tumor in a preious scar. B, Color Doppler scan of a Desmoid tumor in a preious scar reealing some ascularity in the lesion. 图16，A，以前疤痕处的硬纤维瘤。B，彩色多普勒扫描以前瘢痕处的硬纤维瘤病变处显示一些血管供应。
Conclusion： Desmoid tumor showing aggressive growth, with high recurrence rate, should be treated as a soft tissue tumor with low malignancy. 结论：硬纤维瘤呈侵袭性生长，复发率高，治疗应按低度恶性软组织肿瘤处理。
Surgical operation is the optimal treatment, radiotherapy and chemotherapy or endocrine therapy might be effect to desmoid tumor. 外科手术是主要的治疗方法，放疗、化疗和内分泌治疗可能对肿瘤有效。
The desmoid tumor began to grow following these surgeries and became so large that it was compromising his vital organs. 他的硬纤维瘤是在术后开始长出，并且逐步长大以致危及到重要脏器。
A desmoid tumor is an aggressive soft tissue tumor that often invades and destroys surrounding healthy tissue and organs. 硬纤维瘤是一种具有侵袭性的软组织肿瘤，能浸润破坏周围的健康组织和器官。
The estimated incidence of desmoid tumor in the general population is 2 to 4 per million people per year, according to the Desmoid Tumor Research Foundation. 据硬纤维瘤研究基金会的数字，硬纤维瘤在人群中的发病率估计在每年每百万人2-4人。
Objective:To study the biological behavior, clinical pathologic features and prognosis ofvaginal desmoid tumor and try to find out the proper therapy regimens. 目的:研究阴道韧带样纤维瘤的生物学行为、临床病理特征及预后,探讨其治疗方法。
Younger age and female gender had a propensity for local recurrence, suggesting that the biological behavior of desmoid tumor may depend on the status of the disease at presentation. 较年青者和女性有复发倾向，表明韧带样瘤的生物学行为主要依靠疾病特征表现。
The clinical and histological features of desmoid tumors are presented here, with a discussion on management options. 本文针对纤维瘤病的临床、组织学，及处理方法上加以讨论说明。
Objective: To review our experience of management of desmoid tumors of gluteal region in children. 目的：报告13例儿童臀部韧带样瘤的临床资料并讨论其手术治疗问题。
Objective To assess the children desmoid tumors of gluteal region clinical features and treatment methods. 目的探讨小儿臀部侵袭性纤维瘤病的临床特点和手术治疗。
Crook, 61, suffers from Gardner's syndrome, a genetic disorder that can cause multiple polyps and desmoid tumors. 硬纤维瘤是一种具有侵袭性的软组织肿瘤，能浸润破坏周围的健康组织和器官。虽然它不会转移，但是也会威胁生命。
We present 8 cases of pathologically proved abdominal desmoid tumors collected from 1986 to 1991. 摘要自1986年到1991年共收集了8位经病理证实为腹壁纤维瘤之病例。所有病例皆接受电脑断层扫描检查；
Desmoid tumors are rare, locally aggressive but nonmetastasizing fibrous masses that occur sporadically. 摘要腹壁上的硬纤维瘤在临床及病理上属于罕见的软组织瘤，属于典型的低恶性度肿瘤。
Introduction Surgical treatment has been the mainstay for extremity and trunk desmoid tumors with a negative surgical margin. 前言四肢及躯干韧带样瘤手术范围主要依据肿瘤切缘阴性。
We report a 48-year-old woman who underwent operation twelve times for recurrent and multicentric desmoid tumors, and briefly review the literature. 我们报告一个四十八岁的女性病例，在22年来她因为纤维瘤病接受了十二次的手术。