Hu Zongshan, Liu Zhen, Qiu Yong, Xu Leilei, Yan Huang, Zhu Zezhang
Department of Spine Surgery, The Affiliated Drum Tower Hospital of Nanjing, University Medical School, Nanjing, China.
Spine (Phila Pa 1976). 2016 Apr;41(7):598-602. doi: 10.1097/BRS.0000000000001455.
A retrospective study.
Aim of the study was to investigate morphological differences in the vertebrae of scoliosis secondary to neurofibromatosis type 1 (NF1-S) with and without paraspinal neurofibromas and to identify the relationship between paraspinal neurofibromas and vertebral deformity.
Scoliosis is the most common orthopedic manifestation of NF1. Erosion or infiltration of the bone by localized neurofibromas was suggested as one of the primary etiology for the vertebral deformity.
One hundred fourteen patients with NF1-S were classified into spinal tumor (ST) group and nontumor (NT) group with respect to the presence of paraspinal neurofibromas. The curve pattern, curve magnitude, the shape and location of paraspinal neurofibromas, and various kinds of morphological changes of vertebrae were evaluated by complete radiographs were compared between the two groups to determine whether the presence of paraspinal neurofibromas could be associated with a more severe vertebral deformity.
The ST and NT groups included 54 patients (age, 16.8 ± 5.5 years) and 60 patients (age, 17.3 ± 4.2 years), respectively. The Cobb angles of the main curve were 72.3° ± 20.6° and 65.4° ± 19.4° for the ST and NT groups, respectively. No significant differences were observed between the two groups in age, sex ratio, and Cobb angle. There were significant differences between the ST and NT groups in apical vertebral rotation (36.8° ± 7.2° vs. 27.5° ± 6.8°; P < 0.001) and the prevalence of rotatory subluxation (66.1% vs. 35.0%; P = 0.04). Most of the paraspinal neurofibromas (70.4%) developed within the apical region, with the majority (29/38) located on the concave side.
The NF1-S patients with paraspinal neurofibromas had significantly higher prevalence of morphological changes of vertebrae. The paraspinal neurofibromas, most of which were located on the concave side of the apical region, could be associated with more severe vertebral deformities.
一项回顾性研究。
本研究旨在调查1型神经纤维瘤病继发脊柱侧弯(NF1-S)患者中,伴有和不伴有椎旁神经纤维瘤的患者其椎体形态学差异,并确定椎旁神经纤维瘤与椎体畸形之间的关系。
脊柱侧弯是NF1最常见的骨科表现。局部神经纤维瘤对骨质的侵蚀或浸润被认为是椎体畸形的主要病因之一。
114例NF1-S患者根据是否存在椎旁神经纤维瘤分为脊柱肿瘤(ST)组和非肿瘤(NT)组。通过完整的X线片评估两组的侧弯类型、侧弯程度、椎旁神经纤维瘤的形状和位置以及椎体的各种形态学变化,比较两组情况以确定椎旁神经纤维瘤的存在是否与更严重的椎体畸形相关。
ST组和NT组分别包括54例患者(年龄16.8±5.5岁)和60例患者(年龄17.3±4.2岁)。ST组和NT组主弯的Cobb角分别为72.3°±20.6°和65.4°±19.4°。两组在年龄、性别比例和Cobb角方面未观察到显著差异。ST组和NT组在顶椎旋转(36.8°±7.2°对27.5°±6.8°;P<0.001)和旋转半脱位发生率(66.1%对35.0%;P=0.04)方面存在显著差异。大多数椎旁神经纤维瘤(70.4%)发生在顶椎区域内,其中大多数(29/38)位于凹侧。
伴有椎旁神经纤维瘤的NF1-S患者椎体形态学变化的发生率显著更高。椎旁神经纤维瘤大多位于顶椎区域的凹侧,可能与更严重的椎体畸形相关。
3级。