鉴别诊断包括纤维瘤病和软组织的软骨瘤。
The differential diagnosis includes fibromatosis and chondroma of soft parts.
幼年透明蛋白纤维瘤病。
多发性的脊膜瘤可能也伴有神经纤维瘤病。
Multiple meningiomas may also be associated with neurofibromatosis.
目的探讨神经纤维瘤病的MRI影像特征。
目的：探讨儿童头颈部侵袭性纤维瘤病的治疗方法。
Objective: to discuss the therapy of aggressive fibromatosis of head and neck in children.
确切发病原因尚不清楚，多认为与神经纤维瘤病或脂肪瘤退变有关。
The exact pathogenesis of the deformity is still obscure, but most authors believe that macrodactyly is related to neurofibromatosis or lipomata degeneration.
本文对30例多发神经纤维瘤病骨骼改变的X线所见做了分析和讨论。
X-ray findings of the changes of bones with neurofibromatosis in 30 cases are analysed and discussed.
目的检测中国人神经纤维瘤病1型(nf1)基因32、33外显子突变。
Objective to detect the mutation on exons 32, 33 of Chinese the neurofibromatosis type 1 (NF1) gene.
方法回顾分析9例经手术病理证实的侵袭性纤维瘤病的CT和MRI表现。
Methods The CT and MRI studies in 9 cases with pathologically proven AF were retrospectively analyzed.
蝶骨翼发育不良可以是一个孤立性的发现，也可以见于神经纤维瘤病I型患者。
Sphenoid wing dysplasia can occur as an isolated finding or in patients who have Neurofibromatosis type 1. Approximately 50% of cases are associated with neurofibromatosis type 1.
足底纤维瘤病：起源于足底筋膜的纤维增生性病变，为良性病变，但有局部侵袭性。
Plantar fibromatosis: Benign but locally invasive fibrous proliferation originating from the plantar fascia.
两个来自感染腹膜后纤维瘤病的猕猴，另一个来自感染卡波济氏肉瘤的人aids患者。
Two were obtained from macaque monkeys affected with retroperitoneal fibromatosis, the other from human AIDS patients affected with Kaposi's sarcoma.
目的探讨Ⅰ型神经纤维瘤病的临床表现、诊断、治疗，为临床积累经验，提高治疗效果。
Objective To investigate the growth characteristic, clinical manifestations, diagnosis and treatment of neurofibromatosis type 1 (NF1) in oral and maxillofacial regions for the better curative effect.
方法回顾性分析1981 ~ 2005年我科收治的46例周围型神经纤维瘤病的临床资料。
Methods Retrospective analysis of the clinical date was carried out in 46 cases of peripheral neurofibromatosis admitted in our department from 1981 to 2005.
结论 四周型神经纤维瘤病采用整形外科方法切除及修复创面具有切除较彻底、修复塑形好的优点。
Conclusion Plastic surgical treatment of peripheral neurofibromatosis can yield good results with complete excision and better reconstruction.
目的通过人雄激素受体(HUMARA)基因位点克隆性分析技术确定掌纤维瘤病是否为肿瘤性增生。
Objective to study the clonality of palmar fibromatosis by molecular genetic analysis of X chromosome inactivation pattern at a polymorphic site of human androgen receptor gene (HUMARA).
方法：回顾性分析16例神经纤维瘤病性脊柱侧弯患者经过带血管蒂肋骨移植手术治疗后的随访资料。
Methods: The long-term effects of 16 cases of neurofibromatosis scoliosis treated by vascularized grafted rid were analyzed retrospectively.
结果：神经纤维瘤病1型4例，表现为蝶骨大翼缺损2例，其中1例合并双侧桥小脑结合臂胶质瘤，1例合并眶内丛状神经纤维瘤；
Results:Among the4cases of NF1,2had defect of the great wings of the sphenoid, bilateral middle cerebellar peduncle gliomas and plexiform neurofibroma respectively.
分子生物学同样可以检测影响神经功能的许多疾病机理，包括多种毁坏性基因失调：肌肉萎缩症，眼癌，神经纤维瘤症，亨廷顿舞蹈病和某些类阿尔兹·海默症。
Molecular biology has also made it possible to probe the pathogenesis of many diseases that affect neural function, including several.
目的：探讨骨的非骨化性纤维瘤的X线表现，提高对本病的诊断和鉴别诊断水平。
Purpose: to evaluate the X-ray appearances and to improve diagnosis and differential diagnosis of non-ossifying fibroma of bone.
目的：探讨骨的非骨化性纤维瘤的X线表现，提高对本病的诊断和鉴别诊断水平。
Purpose: to evaluate the X-ray appearances and to improve diagnosis and differential diagnosis of non-ossifying fibroma of bone.
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