结缔组织支持和连接着骨骼、韧带和肌肉,并有助于稳定器官位置。硬纤维瘤也被称为侵袭性纤维瘤病(aggressive fibromatosis)或韧带样型纤维瘤病(desmoid-type fibromatosis)。硬纤维瘤非常罕见,约占所有肿瘤的0.03%,占所有软组织肿瘤的不到3%。在一般人群中,硬纤维瘤的估计发病率为每年每百万人口2-4例。 由于结缔组织...
韧带样纤维瘤(desmoid fibromatosis,DF)是一种少见的成纤维细胞克隆性增生性病变,是一种间叶组织来源肿瘤,又称为韧带样瘤、侵袭性纤维瘤病等,发病率为3/100万~4/100万,其特点是具有侵袭性,术后容易复发但不发生转移。DF无完整包膜、呈浸润性生长,2013年WHO软...
韧带样瘤(desmoid tumor) 如何选择 方案 韧带样瘤是发生于肌肉内结缔组织及其被覆的筋膜或腱膜的纤维母细胞性肿瘤。发生于腹壁的就称为腹壁韧带样瘤,腹壁外来源的就称为腹壁外韧带样瘤。其在组织形态上表现良性,但其生物学行为属于低度恶性,呈侵袭性生长、易复发,偶转移。故又称侵袭性纤维瘤病(aggressive fibromat...
Desmoid Tumor/Deep-Seated Fibromatosis (Desmoid-Type Fibromatosis)Gardner syndromeFAPFamilial adenomatous polyposisPregnancyAPCAdenomatous polyposis coliBeta-cateninWntDesmoids are enigmatic clonal malignancies of myofibroblastic cells that do not have the ability to metastasize, but cause morbidity and ...
3. 韧带样纤维瘤 前言:韧带样纤维瘤(desmoid fibromatosis)又称韧带样瘤(desmoid tumor)、侵袭性纤维瘤(aggressive fibromatosis),是一种发生 …www.chemyq.com|基于1 个网页 更多释义 例句 释义: 全部,硬纤维瘤病,带状纤维瘤,韧带样纤维瘤 更多例句筛选 1. Objective To introduce the experience on the diagnosi...
1. Facial infantile aggressive fibromatosis: A frequent localization of an exceptional tumor! [La fibromatose agressive faciale chez l'enfant : Une localisation fréquente d'une tumeur exceptionnelle!] [J] . BouguilaJ., KhonsariR.H., ZitouniK., Annales de chirurgie plastique et esthetique ....
Desmoid tumours (also known as aggressive fibromatosis, desmoid fibromatosis and desmoid-type fibromatosis) are rare, locally invasive, soft tissue tumours that affect approximately 2-4 people in 1 million every year. They can occur anywhere in the body and, though they do not metastasize, they ...
Desmoid fibromatosis (DF) is a rare, non-metastasizing but locally aggressive mesenchymal tumor arising from fibroblasts or myofibroblasts. We report a solitary case ofDF involving the retropharyngeal and danger spaces, a location rarely documented. The patient, a woman in her 70s, presented...
Desmoid Tumor Desmoid tumor, also known asaggressive fibromatosis, is a locally invasive tumor with nometastatic potential. Microscopically, these tumors are characterized by spindle-shaped cells in a collagenous matrix lacking the pleomorphic, atypical, or hyperchromatic nuclei ofmalignancy(Fig. 36-6)...
D’Alteroche L, Benchellal ZA, Salem N, Regimbeau C, Picon L, Metman EH. Complete remission of a mesenteric fibromatosis after taking sulindac Gastroenterol Clin Biol 1998;22:1098–101. PubMedGoogle Scholar Belliveau P, Graham AM. Mesenteric desmoid tumor in Gardner’s syndrome treated by su...