Resection and Reconstruction of a Giant Paranasal Osteoma in a Pediatric Patient

M. Aycart, A. Banwell, Sultan Z. Al-Shaqsi, V. Kratky, N. Wolter, A. Kulkarni, Christopher R. Forrest, J. Riesel
{"title":"Resection and Reconstruction of a Giant Paranasal Osteoma in a Pediatric Patient","authors":"M. Aycart, A. Banwell, Sultan Z. Al-Shaqsi, V. Kratky, N. Wolter, A. Kulkarni, Christopher R. Forrest, J. Riesel","doi":"10.1177/27528464231167306","DOIUrl":null,"url":null,"abstract":"Case Report. Paranasal osteomas are rare, benign bony tumors of the craniofacial skeleton and most are treated endoscopically without the need for reconstruction. In rare cases, open traditional craniofacial approaches are required with a paucity of literature describing extirpative maneuvers in this setting. We present a unique case of a rapidly growing, paranasal bony tumor in a pediatric patient and describe our surgical technique for resection and reconstruction. A 13-year old male presented with eight months of progressive, painless right periorbital swelling and proptosis. Trans-nasal biopsy confirmed an osteoma of the right ethmoid sinus and endoscopic resection was recommended. Due to interval tumor growth, there was worsening visual acuity that precluded a minimally invasive approach. Pre-operative and post-operative 3D computed tomography (CT) scans were completed, and a 3D printed skull model was produced to aid in surgical planning. A multi-disciplinary team of Otolaryngology, Neurosurgery, and Plastic Surgery was employed. The majority of the extirpation was performed with a highspeed carbide burr. Post-operative course was unremarkable and CT scan demonstrated a complete resection. Pathology confirmed the diagnosis of an osteoma. Six-month follow-up demonstrated normal ophthalmologic function and visual acuity with excellent aesthetic results. This is a rare, complex presentation of a paranasal osteoma that was successfully managed with an open, multi-disciplinary approach. We highlight pearls gleaned from this extirpative and reconstructive technique. Due to the tumor density and location, a multidisciplinary team, Stealth navigation, an open, intra- and extra-cranial approach and use of a highspeed carbide burr were essential.","PeriodicalId":314444,"journal":{"name":"Craniomaxillofacial Research & Innovation","volume":"12 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Craniomaxillofacial Research & Innovation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/27528464231167306","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Case Report. Paranasal osteomas are rare, benign bony tumors of the craniofacial skeleton and most are treated endoscopically without the need for reconstruction. In rare cases, open traditional craniofacial approaches are required with a paucity of literature describing extirpative maneuvers in this setting. We present a unique case of a rapidly growing, paranasal bony tumor in a pediatric patient and describe our surgical technique for resection and reconstruction. A 13-year old male presented with eight months of progressive, painless right periorbital swelling and proptosis. Trans-nasal biopsy confirmed an osteoma of the right ethmoid sinus and endoscopic resection was recommended. Due to interval tumor growth, there was worsening visual acuity that precluded a minimally invasive approach. Pre-operative and post-operative 3D computed tomography (CT) scans were completed, and a 3D printed skull model was produced to aid in surgical planning. A multi-disciplinary team of Otolaryngology, Neurosurgery, and Plastic Surgery was employed. The majority of the extirpation was performed with a highspeed carbide burr. Post-operative course was unremarkable and CT scan demonstrated a complete resection. Pathology confirmed the diagnosis of an osteoma. Six-month follow-up demonstrated normal ophthalmologic function and visual acuity with excellent aesthetic results. This is a rare, complex presentation of a paranasal osteoma that was successfully managed with an open, multi-disciplinary approach. We highlight pearls gleaned from this extirpative and reconstructive technique. Due to the tumor density and location, a multidisciplinary team, Stealth navigation, an open, intra- and extra-cranial approach and use of a highspeed carbide burr were essential.
小儿巨大鼻旁骨瘤的切除与重建
病例报告。鼻旁骨瘤是一种罕见的良性颅面骨肿瘤,大多数在内镜下治疗而不需要重建。在极少数情况下,开放的传统颅面入路是必需的,在这种情况下缺乏文献描述切除操作。我们提出一个独特的病例快速增长,鼻旁骨肿瘤在儿童患者和描述我们的手术技术切除和重建。一个13岁的男性提出了八个月进行性,无痛性右眼眶周围肿胀和突出。经鼻活检证实为右筛窦骨瘤,建议行内镜切除。由于间隔期肿瘤生长,视力恶化,妨碍了微创入路。完成术前和术后3D计算机断层扫描(CT),并制作3D打印颅骨模型,以帮助手术计划。由耳鼻喉科、神经外科和整形外科组成的多学科团队参与。大部分的去除是用高速硬质合金毛刺进行的。术后病程无明显变化,CT扫描显示完全切除。病理证实为骨瘤。随访6个月,眼功能和视力正常,美观效果良好。这是一个罕见的,复杂的副鼻部骨瘤,通过开放的,多学科的方法成功地处理。我们重点介绍从这种提取和重建技术中收集的珍珠。由于肿瘤的密度和位置,一个多学科的团队、隐形导航、开放、颅内和颅外入路和使用高速硬质合金毛刺是必不可少的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信