1型神经纤维瘤病患者侧位脑电图蝶鞍测量。

IF 1 Q3 SURGERY GMS Interdisciplinary Plastic and Reconstructive Surgery DGPW Pub Date : 2017-03-23 eCollection Date: 2017-01-01 DOI:10.3205/iprs000107
Reinhard E Friedrich, Johanna Baumann, Anna Suling, Hannah T Scheuer, Hanna A Scheuer
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引用次数: 5

摘要

本研究的目的是测量侧位脑电图上蝶鞍的线段和面积与1型神经纤维瘤病(NF1)患者面部表型的临床诊断。特别注意将测量值与该疾病典型的某些肿瘤类型联系起来。材料和方法:对194例患者进行侧位脑电图调查。考虑到三叉神经的分布规律,根据面神经丛状神经纤维瘤(PNF)的检测和地形进一步对NF1患者进行分类。所有PNF患者均表现单侧肿瘤定位。无面部PNF的患者为另一组。健康志愿者,咬合理想,颌面无任何干预史,作为对照组。在x光片上确定了以下项目:鞍入口、鞍宽度、鞍深度、鞍对角线和鞍面积。结果:三叉神经第一、第二支或所有分支均受影响的PNF患者的蝶鞍测量值增大,具有高度统计学意义。另一方面,PNF仅局限于一个分支或同时存在于第二和第三分支的患者的测量值与没有面部PNF的NF1患者的测量值没有差异。后者与对照组的蝶鞍参数也无差异。结论:本研究为NF1表型与颅底明显的骨骼改变之间的关联提供了证据,这里使用侧位x线片上蝶鞍的表现为例。这些发现也与NF1作为一种骨骼疾病的讨论以及NF1中大脑发育的评估有关。这两项都讨论了与面部丛状神经纤维瘤的关系。此外,了解这些发现之间的关联为临床医生在这些患者的颅底手术计划中提供了相关信息。
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Sella turcica measurements on lateral cephalograms of patients with neurofibromatosis type 1.

The aim of this study was to measure line segments and areas of sella turcica on lateral cephalograms with respect to the clinical diagnosis of facial phenotype of patients with neurofibromatosis type 1 (NF1). Special attention was given to correlate the measured values with certain tumour types that are typical for this disease. Material and methods: Lateral cephalograms of 194 individuals were investigated. Patients with NF1 were further divided according to the detection and topography of facial plexiform neurofibromas (PNF) taking into account the distribution pattern of the trigeminal nerve. All patients with PNF showed unilateral tumour localisation. Patients without any facial PNF constituted a separate group. Healthy volunteers with ideal occlusion and no history of any intervention in the maxillofacial region served as a control group. The following items were determined on the radiographs: sella entrance, sella width, sella depths, sella diagonal, and sella area. Results: Patients with PNF of the first and second trigeminal nerve branch or affected in all branches showed highly statistically significant enlarged sella tucica measurement values. On the other hand, patients with PNF restricted to one branch only or simultaneously in the second and third branches showed measurement values that were not different to those obtained in NF1 patients devoid of facial PNF. The latter group also showed no difference of sella turcica parameters obtained in the control group. Conclusion: This study provides evidence for the association of a certain NF1 phenotype with distinct skeletal alterations of the skull base, shown here using the example of the representation of the sella turcica in the lateral radiograph. These findings are also relevant in the discussion of NF1 as a disease of bones and in the assessment of brain development in NF1. Both items are discussed in relationship to a facial plexiform neurofibroma. Furthermore, the knowledge of this association of findings provides the clinician with relevant information in the planning of skull base procedures in these patients.

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