患有面部丛状神经纤维瘤的 1 型神经纤维瘤病患者前后头颅影像中的下颌骨对称性。

IF 1 Q3 SURGERY
Reinhard E Friedrich, Georg Christ, Hanna A Scheuer
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引用次数: 0

摘要

简介神经纤维瘤病 1 型(NF1)是一种常染色体显性遗传性肿瘤易感综合征。外周神经鞘瘤(PNST)是 NF1 的特征之一。丛状神经纤维瘤(PNF)是 NF1 特征性肿瘤,通常会导致毁容(如面部),被认为是癌前病变。以往的研究表明,面部 NF1(FPNF)对面部骨骼的形状有影响。本研究考虑到 FPNF 的地形,研究了下颌骨对称性与头颅测量参考平面的偏差:对 168 名 NF1 患者的前后(PA)头影进行了检查。我们对三组患者进行了比较:FPNF 患者(74 人)、播散性皮肤神经纤维瘤(DNF,94 人)和无 NF1 的对照组(23 人)。PNF组根据面部PNST类型和位置进行了分型。确定了典型的下颌骨头骨测量参考点(髁状突、前髁突和门突):结果:FPNF 患者的下颌骨骨骼测量点往往与 DNF 组的测量点有明显差异。事实证明,中线-矢状线测量点的典型不对称是 PNF 的指标。测量值显示三叉神经肿瘤扩散模式的差异。研究结果表明,局部肿瘤效应(PNF)对测量点与参考平面之间的关系具有可信性。研究证明,肿瘤类型(FPNF)和受 FPNF 影响的三叉神经分支数量可能与下颌骨在 PA 投影上明显偏离对称性有关:本研究结果表明,下颌骨畸形的特征模式可通过标准化 X 光片测量出。标准X光片显示的下颌骨畸形可能是以前未被发现的NF1的初步指标。下颌骨的肿瘤相关改变应在NF1病理诊断先驱骨性发现的分类系统中予以考虑。放射学检查结果为规划 NF1 患者的下颌骨截骨手术提供了线索,尤其是在评估因肿瘤扩散而典型高血管化的面部区域时。此外,放射学检查结果还表明肿瘤可能会侵犯和破坏邻近的咀嚼肌和模仿肌,这些结果可能会对手术措施(功能、美观和伤口愈合)产生影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mandibular symmetry on posterior-anterior cephalograms of neurofibromatosis type 1 patients with facial plexiform neurofibroma.

Introduction: Neurofibromatosis type 1 (NF1) is an is an autosomal dominant heritable tumor predisposition syndrome.. Peripheral nerve sheath tumors (PNST) are a hallmark of NF1. Plexiform neurofibromas (PNF) are neoplasms that are characteristic of NF1, often causing disfiguring effects (e.g., on the face), and are considered precancerous lesions. Previous studies have shown that facial PNF (FPNF) have an impact on the shape of facial bones. This study examines deviations of mandibular symmetry from cephalometric reference planes considering the topography of FPNF.

Material and methods: The posterior-anterior (PA) cephalograms of 168 patients with NF1 were examined. We compared three groups: patients with FPNF (n=74), with disseminated cutaneous neurofibroma (DNF (n=94)), and control subjects without NF1 (n=23). The PNF group was subtyped with respect to facial PNST type and location. Typical mandibular cephalometric reference points were determined (condyle, antegonion, and menton).

Results: The skeletal measurement points of the mandible in FPNF patients often differ significantly from those of the DNF group. It has been proven that typical asymmetries of the median-sagittal measurement points are indicators of PNF. Differences within the trigeminal tumor spread patterns are indicated in the measured values. A local tumor effect (PNF) on the relation of the measurement points to the reference planes is made plausible by the study results. The investigations prove that tumor type (FPNF) and the number of FPNF affected branches of the trigeminal nerve may correlate with significant deviations of mandible from symmetry on PA projections.

Conclusion: The presented study shows that characteristic patterns of mandibular deformity can be measured on standardized radiographs in NF1 patients with FPNF. Mandibular deformities imaged on standardized radiographs may be initial indicators of a previously unrecognized NF1. Tumor-associated alterations of the mandible should be considered in the classification systems of pathognomonic, diagnostically pioneering osseous findings in NF1. The radiological findings provide clues for planning mandibular osteotomies in NF1 patients, especially for assessing facial regions typically highly vascularized by tumor spread. Furthermore, the radiological findings are an indication of a tumor potentially invading and destroying adjacent masticatory and mimic muscle, findings that may have an influence on surgical measures (function, aesthetics, and wound healing).

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