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.
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.
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.
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.
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.
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.
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.
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