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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。
- Keywords Familial adenomatous polyosis （FAP）;Desmoid tumor（DT）; 家族性腺瘤性息肉病;硬纤维瘤;
- 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。
