纤维瘤病

基本解释 (translations)

fibromatosis

与纤维瘤病相关的网络例句 [注：此内容来源于网络，仅供参考]

Resulte: In 12 infective lesions, including purulent infection (4 cases) and tuberculosis (8 cases), the correct dignosis was made in 4cases by CR and in 11 cases by CT. In 16 soft tissue tumors, including lipoma (7 cases), fibrosarcoma (4 cases), hemangioma (1 case), neurofibroma (1 case), malignant fibrous histocytoma (1case), aggressive fibromatosis (1 case) and liposarcoma (1 case), the correct diagnosis was made in 3cases by CR and in 14 cases by CT. In 11 bone lesions, including fibrous dysplasia (7 cases), chondroma (2 cases), myeloma and cosinophilic granuloma (1 case), the correct diagnosis was made in 8cases by CR and in 10 cases by CT.

结果：感染组12例中(包括化脓性感染4例，胸壁结核8例)，CR准确诊断4例，CT诊断11例；软组织肿瘤组16例中(包括脂肪瘤7例，纤维肉瘤4例，血管瘤、神经纤维瘤、恶性纤维组织细胞瘤、侵袭性纤维瘤病和脂肪肉瘤各l例)，CR准确诊断3例，CT诊断14例；骨肿瘤和肿瘤样病变组11例中(包括骨纤维异常增殖症7例，软骨瘤2例，多发性骨髓瘤和骨嗜酸性肉芽肿各1例)，CR准确诊断8例，CT诊断10例。

Aggressive fibromatosis is a disease of benign ,clone hyperplasia of fibrocyte.β-catenin,which starts downstream gene transcription,was found concentrated in cell nuclei in sporadic patients.

侵袭性纤维瘤病是一种良性克隆性纤维细胞增生疾病，在散发病人的组织病理切片中发现β-catenin向细胞核内浓聚，即向核内转移启动下游基因转录。

Clinical diagnostic considerations ranged from benign entities such as rhabdomyoma, intramuscular lipoma, fibromatosis, myositis ossificans, proliferative myositis, inflammatory myofibroblastic tumor, and inflammatory myopathy to malignant entities such as rhabdomyosarcoma, leiomyosarcoma, liposarcoma, and lymphoma.

这些病例的临床考虑多样，有良性的横纹肌瘤、肌内脂肪瘤、纤维瘤病、骨化性肌炎、增生性肌炎、炎性肌纤维母细胞瘤和炎性肌病，也有恶性的横纹肌肉瘤、平滑肌肉瘤、脂肪肉瘤和淋巴瘤。

Results All the 7 cases were female, 2 cases were solitary fibrous tumor, 2 cases were myofibroblastoma, 1 case was inflammatory myofibroblastic tumour, 1 case was fibromatosis, and 1 case was low grade myofibroblastic sarcoma.

结果 7例患者均为女性，2例为孤立性纤维性肿瘤；2例为肌纤维母细胞瘤；1例为纤维瘤病；1例为炎性肌纤维母细胞瘤；1例为低度恶性肌纤维母细胞肉瘤。

Nestin is a novel marker for GISTs following CD117, It could be efficient in the differerntial diagnosis between GISTs and leiomyomas or fibromatosis. However, other antibody such as S-100 should be used in the differential diagnosis between GISTs and Schwannomas.

nestin是辅助诊断GISTs的新指标，可鉴别GISTs与平滑肌肿瘤和纤维瘤病，但在GISTs与雪旺瘤的鉴别中需结合S-100蛋白等指标。

Results Among 96 cases of CD117-positive GISTs, 94 positive for nestin (in amount of this 70 diffusive positive, 21 moderate positive, 3 local positive), the other two were negative. 4 of the 5 CD117-negative GISTs and 26 of 33 Schwannomas expressed nestin too, only 3 of 15 leiomyosarcomas showed focal positive for nestin. All oesophagus leiomyomas and fibromatosis of intestinal demonstrated negativity for nestin.

结果 96例CD117阳性的GISTs中，94例表达nestin，其中70例弥漫强表达，21例中度阳性，3例局灶阳性，仅2例阴性；5例CD117阴性的GISTs中，4例表达nestin；33例消化道雪旺瘤中26例表达nestin；15例平滑肌肉瘤中3例局灶表达nestin；10例食管平滑肌瘤、6例肠纤维瘤病均为阴性。

Methods There were 165 cases of mesenchymal tumors were investigated the expression of nestin by immunohistochemistry, including 96 CD117-positive GISTs, 5 CD117-negative GISTs, 10 oesophagus leiomyomas, 33 digestive tract Schwannomas, 6 fibromatosis and 15 leiomyosarcomas in abdominal cavity.

用免疫组化EnVi-sion法检测96例CD117阳性、5例CD117阴性的GISTs，以及食管平滑肌瘤（10例）、消化道雪旺瘤（33例）、肠纤维瘤病（6例）以及腹腔平滑肌肉瘤（15例），观察这些肿瘤中nestin的表达状况。

Adenomatous polyposis coli; Fibromatosis, aggressive ; Diagnosis; Therapeutics

腺瘤息肉病，结肠纤维瘤病，侵袭型诊断治疗学

Methods Nuclear β-catenin expression was detected by immunohistochemistry in 77 lesions with desmoid-type fibromatosis and 171 other spindle cell lesions, including superficial fibrmoatosis (n=18), nodular fasciitis (n=36), keloid (n=16), scar (n=10), granulation tissue (n=9), synovial sarcoma (n=38), neufibroma (n=13), solitary fibrous tumor (n=12), gastrointestinal stromal tumor (n=10), low-grade myxofibrosarcoma (n=3), low-grade fibromyxoid sarcoma (n=3), and smooth muscle tumor (n=10). In addition, the immunohistochemical expressions of ER-α, ER-β and Ki-67 were examined in all of the lesions with desmoid-type fibromatosis. The nuclear immunohistochemical staining for nuclear βcatenin and ER-β was graded as high level (≥25% of cells), low level (5%-25%) or none.

采用免疫组织化学染色法检测77例韧带样型纤维瘤病和171例其它良、恶性梭形细胞病变（包括结节性筋膜炎36例、浅部纤维瘤病11例、瘢痕疙瘩16例、增生性瘢痕10例、肉芽组织9例、滑膜肉瘤38例、神经纤维瘤13例、孤立性纤维性肿瘤12例、胃肠间质肿瘤10例、低度恶性黏液纤维肉瘤3例、低度恶性纤维黏液样肉瘤3例及平滑肌肿瘤10例）组织中β-catenin核阳性的表达，同时检测韧带样型纤维瘤病中ER-α、ER-β和Ki-67的表达。

In contrast to plexiform neurofibromas, plexiform schwannoma is only weakly associated with neurofibromatosis type 1 (von Recklinghausen's disease), and has little malignant potential.

相对於丛状神经纤维瘤，丛状神经鞘瘤与第一型予纤维瘤病(neurofibromatosis type 1，von Recklinghausen's disease)的相关很薄弱，而且没有恶性变化的倾向。

与纤维瘤病相关的网络解释 [注：此内容来源于网络，仅供参考]

desmoid tumor：韧带状瘤

<正> 本病又称韧带状瘤(desmoid tumor)或侵袭性纤维瘤病(aggressive fibromatosis),是介于良恶性之间的纤维性肿瘤. 其特点为纤维组织的增生并形成瘤样病变,增生的纤维组织较为成熟,与纤维瘤相似,但无包膜. 病变源自肌筋膜,常呈浸润性生长,

fibromatoid：纤维瘤病

纤维瘤样的 fibroma virus | 纤维瘤病 fibromatoid | 纤维黏液瘤 fibromatosis

fibromatoid nodular fasciitis：纤维瘤样型结节性筋膜炎

fibromatoid 纤维瘤样的 | fibromatoid nodular fasciitis 纤维瘤样型结节性筋膜炎 | fibromatosis 纤维瘤病,瘤样纤维组织增生

fibromatosis：纤维瘤病

瘤病(-omatosis)常用于多发性良性肿瘤,如神经纤维瘤病(neurofibromatosis);或用于在局部呈弥漫性生长的良性肿瘤,如纤维瘤病(fibromatosis)、脂肪瘤病(lipomatosis)和血管瘤病(angiomatosis)等.

plantar fibromatosis：足底纤维瘤病

plantar fascia 跖腱膜 | plantar fibromatosis 足底纤维瘤病 | plantar fibrositis 跖纤维织炎

aggressive fibromatosis：侵袭性纤维瘤病

硬纤维瘤(Desmoid tumors):好发於年轻人,又称侵袭性纤维瘤病(aggressive fibromatosis). 以广泛切除(wide excision)为主,放射线治疗可增加局部控制. 药物治疗亦可尝试Tamoxifen、非发炎性止痛药、干扰素及化学治疗.

cicatrical fibromatosis：瘢痕性纤维瘤病

瘢痕挛缩 cicatrisation | 瘢痕性纤维瘤病 cicatrical fibromatosis | 瘤外综合征 paraneoplastic syndrome

fibromatosis colli：颈部纤维瘤病,颈部纤维瘤病

fibromatosis 纤维瘤病,瘤样纤维组织增生 | fibromatosis colli 颈部纤维瘤病,颈部纤维瘤病 | fibromatosis diffusa 弥漫性纤维瘤病

fibromatosis diffusa：弥漫性纤维瘤病

fibromatosis colli 颈部纤维瘤病,颈部纤维瘤病 | fibromatosis diffusa 弥漫性纤维瘤病 | fibromatosis gingiva 龈纤维瘤病

fibromatous：纤维瘤的

fibromatosis gingiva 龈纤维瘤病 | fibromatous 纤维瘤的 | fibromuscular dysplasia of cerebral artery 脑动脉纤维肌肉发育异常