纤维瘤病

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。

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

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。

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 .

神经纤维瘤病Ⅰ型累及脊柱脊髓的MR表现

MR Imaging of intramedullary and spinal canal tumors with neurofibromatosis type 1

目的分析侵袭性纤维瘤病的CT表现，了解其影像特征。

Objective To clarify the CT characteristics of aggressive fibromatosis .

方法回顾性分析8例儿童臀部纤维瘤病的CT表现。

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

神经纤维瘤病颅脑和脊柱CT、MRI表现

CT and MRI manifestations of neurofibromatosis in cranium and spinal column

儿童臀部纤维瘤病的CT表现与病理对照

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

神经纤维瘤病Ⅱ型的MRI表现及在临床诊断中的作用

MRI image of neurofibromatosis type 2 and its application in clinical diagnosis

II型神经纤维瘤病的MRI表现（附6例报道）

MRI diagnosis of neurofibromatosis type II ( report of 6 cases )

侵袭性纤维瘤病的CT与MRI表现

CT and MRI manifestations of aggressive fibromatosis

侵袭性纤维瘤病的CT诊断

CT Diagnosis of Aggressive Fibromatosis

神经纤维瘤病的脑部CT评价

CT evaluation of intracranial neurofibromatosis

目的：研究神经纤维瘤病的中枢神经系统MRI表现。

Objective : To study the MRI appearance of central nervous system in neurofibromatosis .

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。

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

神经纤维瘤病II型与听觉脑干植入

Neurofibromatosis type 2 and Auditory Brainstem Implantation

神经纤维瘤病I型的MRI研究

MRI study of neurofibromatosis type I

婴儿型肌纤维瘤病的临床特点Sweet综合征伴鞘膜积液及附睾炎

Clinical characteristics of infantile myofibromatosis Sweet 's syndrome with hydrocele and epididymitis : a case report

神经纤维瘤病的MRI诊断

MRI diagnosis of neurofibromatosis

材料与方法：收集12例神经纤维瘤病患者的临床资料并对其MRI表现进行分析。

Materials and Methods : This study included 12 patients of neurofibromatosis , the MRI findings were analyzed .

目的：强调Ⅱ型神经纤维瘤病头部MRI的诊断和增强扫描价值。

Objective : To emphasize the diagnostic value of cranial MRI examination and enhanced scanning in neurofibromatosis type ⅱ .

结论：MRI是目前诊断神经纤维瘤病的最佳影像学检查方法，优于CT。

Conclusion : MRI can be considered as first choice of study in diagnosing of neurofibromatosis , it is superior to CT .

目的：认识神经纤维瘤病Ⅰ型的颅脑影像学表现，评价MRI和CT在诊断方面的价值。

Purpose : To understand cranial involvement of neurofibromatosis type I and to evaluate the value of CT and MRI in diagnostic aspect .

马尾神经鞘瘤16例MRI诊断分析40～49岁组发病率最高为28.78%，神经纤维瘤病患者并发神经鞘瘤占神经鞘瘤的1.66%。

Diagnostic Analysis of MRI in 16 Patients with Neurilemoma of Cauda Equina The incidence of neurofibromatosis in neurilemoma was 1.66 % .

目的认识神经纤维瘤病的颅脑及脊柱MRI表现，为临床进一步诊治提供客观依据。

Objective To understand MRI findings of neurofibromatosis in cranium and spinal column is helpful in providing reliable informations for further clinical management .

材料与方法：搜集我院行MR检查并经手术证实符合神经纤维瘤病诊断标准者3例，分析其头部MRI表现。

Materials and Methods : We collected 3 cases of neurofibromatosis type ⅱ proven by surgery and MR imaging system . The cranial MR appearences were reported .

结论CPT是一种非神经起源的病变，它的发病与神经纤维瘤病无直接关系；

Its occurrence has no direct relation with neurofibromatosis .

韧带样型纤维瘤病Wnt通路中APC/β-catenin基因异常

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

p-AKT和PTEN在Ⅰ型神经纤维瘤病中的表达及意义

Effect of p-AKT and PTEN on Neurofibromatosis ⅰ Pathogenesis

目的探讨耳鼻咽部多发性神经纤维瘤病（neurofibromatosis，NF）的病理、临床表现及诊断和治疗。

Objective To investigate the growth characteristic , clinical manifestation , diagnosis and treatment of neurofibromatosis ( NF ) in otorhinolaryngology .

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）。

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 ) .