fibromatosis

  • n.纤维瘤病
fibromatosisfibromatosis
  1. 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。

  2. Purpose To study the clinicopathological characteristics , treatment and prognosis of infantile fibromatosis ( IF ) .

    目的探讨婴幼儿纤维瘤病(infantilefibromatosis,IF)的临床病理特点、治疗及预后。

  3. Clinical Analysis of 19 Cases with Children Aggressive Fibromatosis

    小儿侵袭性纤维瘤病19例临床分析

  4. A Clinical Study on 20 Cases with Aggressive Fibromatosis

    侵袭性纤维瘤20例临床分析

  5. 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。

  6. Evaluation of High-frequency Color Doppler Ultrasonography in Diagnosis of Abdominal Wall Fibromatosis

    高频彩色多普勒超声对腹壁纤维瘤病的诊断价值

  7. Objective To clarify the CT characteristics of aggressive fibromatosis .

    目的分析侵袭性纤维瘤病的CT表现,了解其影像特征。

  8. Clinicopathological Study on Desmoid Type Fibromatosis : A Report of 21 cases

    韧带样型纤维瘤病21例临床病理分析

  9. Spontaneous isolated fibromatosis of mesentery : two cases report with review of the literature

    自发性孤立性肠系膜纤维瘤病2例报道及文献复习

  10. Methods CT manifestations of child gluteal aggressive fibromatosis were retrospectively analyzed .

    方法回顾性分析8例儿童臀部纤维瘤病的CT表现。

  11. A study of the ultrastructure and gene location of hereditary gingival fibromatosis

    遗传性牙龈纤维瘤病超微结构及基因定位研究

  12. Hereditary gingival fibromatosis : case report and literature review

    遗传性牙龈纤维瘤临床报道及文献回顾侵袭性纤维瘤病

  13. Child gluteal aggressive fibromatosis : a correlative study of CT findings and pathology

    儿童臀部纤维瘤病的CT表现与病理对照

  14. Aggressive Fibromatosis of the Orbit and Literature Review

    侵袭性眼眶纤维瘤病及文献复习

  15. CT and MRI manifestations of aggressive fibromatosis

    侵袭性纤维瘤病的CT与MRI表现

  16. Exclusive Gene Location of Hereditary Gingival Fibromatosis

    遗传性牙龈纤维瘤病致病基因的排除性定位

  17. CT Diagnosis of Aggressive Fibromatosis

    侵袭性纤维瘤病的CT诊断

  18. Clinic analysis of hereditary gingival fibromatosis

    遗传性牙龈纤维瘤病的临床病例分析

  19. The clinical and pathological factors mentioned above should be considered on judging the risk of recurrence of abdominal fibromatosis in making an appropriate therapeutic strategy .

    临床上应根据上述临床病理因素判断复发风险,提供合适的治疗方案。

  20. Purpose : To compare abdominal fibromatosis with extraabdominal fibromatosis and to study the CT findings of the latter .

    目的:对侵袭性纤维瘤病的腹壁外组及腹壁组作比较,重点讨论腹壁外侵袭性纤维瘤病的CT表现。

  21. Abnormalities of APC gene / β - catenin gene in Wnt pathway in desmoid-type fibromatosis

    韧带样型纤维瘤病Wnt通路中APC/β-catenin基因异常

  22. Conclusion : Hereditary gingival fibromatosis in our study is dominantly inherited and presents mainly as non-syndromic form , with high penetrance and variable expressivity .

    结论:收集的5个家系均为非综合征型常染色体显性遗传HGF,且疾病外显率高,表现度变异大。

  23. High positive expression of type I collagen was noted in the normal periosteum . High positive expression of type III Collagen was noted in fibromatosis and the periosteum of CPT ( P0.05 ) .

    未见神经成分,血管罕见八2)组织化学研究发现正常骨膜中以1型胶原为主,CPT病变骨膜及纤维瘤病病变组织中以*型胶原为主(P<0.05)。

  24. To investigate the disorder of Wnt signal transduction pathway in tumorigenesis , we studied the adenomatous polyposis coli ( APC ) gene and β - catenin gene mutations in desmoid-type fibromatosis .

    本研究分析了韧带样型纤维瘤病中APC和-βcatenin基因突变,探讨Wnt通路中APC/β-catenin基因异常在肿瘤发生中的作用。

  25. Conclusions : There are somatic mutations of APC and β - catenin gene in desmoid-type fibromatosis , abnormal expression of β - catenin protein increase can be observed in the cytoplasm and nucleus , and results in the higher expression of c-myc protein .

    结论:韧带样型纤维瘤病中APC、β-catenin基因存在体系突变,β-catenin蛋白存在异常表达,可能引起c-myc表达增加。

  26. Objective : Hereditary gingival fibromatosis ( HGF ) is an exceptional gingival benign lesion , which is characterized by diffuse and gradual hyperplasia . Its etiology and pathogenesis are not clearly understood . A case of child HGF who complained of gingival overgrowth is reported .

    目的:遗传性牙龈纤维瘤病(hereditarygingivalfibromatosis,HGF)是一种罕见的以牙龈组织弥漫性、渐进性增生为主要特征的良性病变,发病机制和临床表现较为复杂,至今仍病因不明。