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[1型神经纤维瘤病中上颌窦的异常情况]

[Abnormalities of the maxillary sinus in type 1 neurofibromatosis].

作者信息

Friedrich R E, Giese M, Mautner V F, Schmelzle R, Scheuer H A

机构信息

Klinik für Mund-, Kiefer- und Gesichtschirurgie, Nordwestdeutsche Kieferklinik, Universitätsklinikum Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg.

出版信息

Mund Kiefer Gesichtschir. 2002 Sep;6(5):363-7. doi: 10.1007/s10006-002-0417-0.

Abstract

AIM

The aim of this study was to determine the malformations of the maxillary sinus in neurofibromatosis type 1 patients (NF1).

MATERIAL AND METHODS

Twenty-two patients with NF1 were investigated clinically and radiologically: 11 had an unilateral trigeminal plexiform neurofibroma and 11 had multiple cutaneous neurofibromas. The histological type of NF was ascertained in all cases following tumor resections. The malformation of the maxillary sinus was assessed on plain radiographs and computed or magnetic resonance tomograms. Intraindividual side comparison was used to judge the size of the sinus and its position in the midface.

RESULTS

In patients with cutaneous neurofibromas the maxillary sinus appeared symmetrical in size and position. The pneumatization of the sinus had no abnormalities on the radiographs. Malformations of the maxillary sinus were restricted to plexiform neurofibromas. On the side affected by a plexiform NF, the sinus appeared hypoplastic and caudally displaced due to an enlarged ipsilateral orbit. The expansion of the sinus to the lateral side was impaired, obviously due to tumor masses. Consecutively, the alveolar process of the affected side was also displaced leading to a complex malocclusion.

DISCUSSION

Malformations of the face are frequently presented as case reports in the literature. Emphasis is given to the elephantiasis-like tumor growth of the face in certain patients with NF1. The underlying pathology has not yet been fully understood. This report provides evidence that in the midfacial region the overgrowth is predominantly caused by the plexiform neurofibroma itself and that the bones can even be hypoplastic and show scoliosis-like malformation compared to the nonaffected side. These findings are relevant when debulking procedures of the face are planned for NF1 patients.

摘要

目的

本研究旨在确定1型神经纤维瘤病(NF1)患者上颌窦的畸形情况。

材料与方法

对22例NF1患者进行了临床和影像学检查:11例患有单侧三叉神经丛状神经纤维瘤,11例患有多发性皮肤神经纤维瘤。所有病例在肿瘤切除后确定NF的组织学类型。通过X线平片、计算机断层扫描或磁共振断层扫描评估上颌窦的畸形情况。采用个体内双侧比较来判断窦的大小及其在面中部的位置。

结果

在患有皮肤神经纤维瘤的患者中,上颌窦在大小和位置上表现对称。鼻窦的气化在X线片上无异常。上颌窦畸形仅限于丛状神经纤维瘤。在受丛状神经纤维瘤影响的一侧,由于同侧眼眶增大,鼻窦显得发育不全且向尾侧移位。鼻窦向外侧的扩展受到损害,显然是由于肿瘤肿块所致。随之,患侧的牙槽突也发生移位,导致复杂的错牙合畸形。

讨论

面部畸形在文献中常以病例报告的形式呈现。重点关注某些NF1患者面部象皮肿样的肿瘤生长。其潜在病理尚未完全明确。本报告提供的证据表明,在面中部区域,过度生长主要由丛状神经纤维瘤本身引起,与未受影响侧相比,骨骼甚至可能发育不全并呈现脊柱侧凸样畸形。当为NF1患者计划面部减容手术时,这些发现具有重要意义。

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