• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

患者患有 1 型神经纤维瘤病,其下颌骨中存在巨细胞性肉芽肿和神经纤维瘤:具有放射学和外科方面的长期随访病例报告,并进行文献复习。

Giant cell granuloma and neurofibroma in the mandible of a patient with neurofibromatosis type 1: a long-term follow-up case report with radiological and surgical aspects and a review of the literature.

机构信息

Oral and Maxillofacial Radiology, Umeå University Hospital, Umeå, Sweden.

Oral and Maxillofacial Radiology, Department of Odontology, Umeå University, Umeå, Sweden.

出版信息

BMC Oral Health. 2024 Jul 14;24(1):792. doi: 10.1186/s12903-024-04543-9.

DOI:10.1186/s12903-024-04543-9
PMID:39004713
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11247863/
Abstract

BACKGROUND

Magnetic resonance imaging (MRI) of the brain is frequently performed on patients with neurofibromatosis type 1 (NF1), to detect and follow-up intracranial findings. In addition, NF1-related pathologies can appear in the jaws. This case study investigates if it is advantageous to assess the depicted parts of the jaws in the imaging of NF1 patients with intracranial findings, thereby detecting jaw pathologies in their initial stages.

CASE PRESENTATION

We report on the 3-year management with clinical and radiological follow-ups of a central giant cell granuloma and a neurofibroma in the mandible of a patient with NF1 who underwent examinations with brain MRIs. A review of the mandible in the patient's MRIs disclosed lesions with clear differences in progression rates.

CONCLUSION

NF1-related jaw pathologies may be detected in the early stages if the depicted parts of the jaws are included in the assessment of the imaging of NF1 patients with intracranial findings. This could impact the treatment of eventual pathologies before lesion progression and further damage to the vicinity.

摘要

背景

磁共振成像(MRI)常用于神经纤维瘤病 1 型(NF1)患者,以检测和随访颅内病变。此外,NF1 相关病变也可能出现在颌骨中。本病例研究旨在探讨在有颅内病变的 NF1 患者的影像学检查中评估颌骨的相关部位是否有助于在早期发现颌骨病变。

病例介绍

我们报告了一例 NF1 患者,其下颌中存在中央性巨细胞瘤和神经纤维瘤,通过脑部 MRI 检查进行了 3 年的临床和影像学随访。对患者 MRI 中下颌骨的回顾显示,病变的进展速度有明显差异。

结论

如果在评估有颅内病变的 NF1 患者的影像学检查时包括颌骨的相关部位,则可能在早期发现 NF1 相关的颌骨病变。这可能会影响对潜在病变的治疗,避免病变进展和周围组织进一步受损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/09d7716a1098/12903_2024_4543_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/a1ad497ee28f/12903_2024_4543_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/0144c55d05ce/12903_2024_4543_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/5e03977a8cf1/12903_2024_4543_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/cbb93d43b9f6/12903_2024_4543_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/91bf504dae52/12903_2024_4543_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/3d7794407a66/12903_2024_4543_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/09d7716a1098/12903_2024_4543_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/a1ad497ee28f/12903_2024_4543_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/0144c55d05ce/12903_2024_4543_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/5e03977a8cf1/12903_2024_4543_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/cbb93d43b9f6/12903_2024_4543_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/91bf504dae52/12903_2024_4543_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/3d7794407a66/12903_2024_4543_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60f6/11247863/09d7716a1098/12903_2024_4543_Fig7_HTML.jpg

相似文献

1
Giant cell granuloma and neurofibroma in the mandible of a patient with neurofibromatosis type 1: a long-term follow-up case report with radiological and surgical aspects and a review of the literature.患者患有 1 型神经纤维瘤病,其下颌骨中存在巨细胞性肉芽肿和神经纤维瘤:具有放射学和外科方面的长期随访病例报告,并进行文献复习。
BMC Oral Health. 2024 Jul 14;24(1):792. doi: 10.1186/s12903-024-04543-9.
2
Neurofibromatosis type 1 associated with bilateral central giant cell granuloma of the mandible.神经纤维瘤病 1 型合并下颌骨双侧中央性巨细胞肉芽肿。
J Craniomaxillofac Surg. 2011 Oct;39(7):538-43. doi: 10.1016/j.jcms.2010.10.014. Epub 2010 Nov 11.
3
Recurrent multilocular mandibular giant cell granuloma in neurofibromatosis type 1: Evidence for second hit mutation of NF1 gene in the jaw lesion and treatment with curettage and bone substitute materials.1型神经纤维瘤病中的复发性多房性下颌骨巨细胞肉芽肿:颌骨病变中NF1基因二次打击突变的证据及刮除术和骨替代材料治疗
J Craniomaxillofac Surg. 2016 Aug;44(8):1054-60. doi: 10.1016/j.jcms.2016.05.010. Epub 2016 May 15.
4
A combination of skeletal deformations of the dorsal mandible and temporomandibular region detected in orthopantomograms of patients with neurofibromatosis type 1 indicates an associated ipsilateral plexiform neurofibroma.在 1 型神经纤维瘤病患者的全景片中检测到的下颌骨背侧和颞下颌区域的骨骼畸形组合表明存在同侧丛状神经纤维瘤。
J Craniomaxillofac Surg. 2018 Jul;46(7):1091-1104. doi: 10.1016/j.jcms.2018.04.018. Epub 2018 Apr 26.
5
Idiopathic bilateral central giant cell reparative granuloma of jaws: a case report and literature review.特发性双侧颌骨中央巨细胞修复性肉芽肿:一例报告及文献复习
Int J Pediatr Otorhinolaryngol. 2010 May;74(5):547-52. doi: 10.1016/j.ijporl.2010.02.006. Epub 2010 Mar 12.
6
An aggressive central giant cell granuloma in a pediatric patient: case report and review of literature.儿童患者侵袭性中央性骨巨细胞瘤:病例报告及文献复习。
J Otolaryngol Head Neck Surg. 2019 Jul 18;48(1):32. doi: 10.1186/s40463-019-0356-5.
7
Non-odontogenic Intraosseous Radiolucent Lesions of the Mandibular Body Are Rare Findings on Panoramic Views of Patients With Neurofibromatosis Type 1.1型神经纤维瘤病患者全景片中,下颌骨体部非牙源性骨内透射性病变是罕见表现。
Anticancer Res. 2019 Apr;39(4):1971-1985. doi: 10.21873/anticanres.13308.
8
A fortuitous discovery of a neurofibroma in a female patient with type 1 neurofibromatosis: a case report.一名 1 型神经纤维瘤病女性患者偶然发现神经纤维瘤:病例报告。
J Int Med Res. 2022 Dec;50(12):3000605221139716. doi: 10.1177/03000605221139716.
9
Giant cell reparative granuloma of the mandible with an aggressive radiological appearance.下颌骨巨细胞修复性肉芽肿,具有侵袭性影像学表现。
Ann R Coll Surg Engl. 2020 Mar;102(3):e75-e76. doi: 10.1308/rcsann.2019.0174. Epub 2019 Dec 18.
10
Combined central odontogenic fibroma and giant cell granuloma-like lesion of the mandible: report of a case and review of the literature.下颌骨中央性牙源性纤维瘤合并巨细胞肉芽肿样病变:1例报告及文献复习
J Oral Maxillofac Surg. 1999 Oct;57(10):1258-62. doi: 10.1016/s0278-2391(99)90500-1.

本文引用的文献

1
Recurrent Mandibular Giant Cell Lesion in Neurofibromatosis Type 1: Second Hit Mutation on the Gene in the Osseous Lesion.1 型神经纤维瘤病中复发性下颌巨大细胞瘤:骨病变中 基因的二次打击突变。
Anticancer Res. 2022 Jun;42(6):2945-2952. doi: 10.21873/anticanres.15777.
2
Epidemiological profile and clinical characteristics of 491 Brazilian patients with neurofibromatosis type 1.491 例巴西神经纤维瘤病 1 型患者的流行病学特征和临床特征。
Brain Behav. 2022 Jun;12(6):e2599. doi: 10.1002/brb3.2599. Epub 2022 May 4.
3
Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Familial Tumor Syndromes.
世界卫生组织头颈部肿瘤分类第五版更新:家族性肿瘤综合征。
Head Neck Pathol. 2022 Mar;16(1):143-157. doi: 10.1007/s12105-022-01414-z. Epub 2022 Mar 21.
4
Non-Oncological Neuroradiological Manifestations in NF1 and Their Clinical Implications.神经纤维瘤病1型的非肿瘤性神经放射学表现及其临床意义
Cancers (Basel). 2021 Apr 12;13(8):1831. doi: 10.3390/cancers13081831.
5
Management of Central Giant Cell Granulomas of the Jaws: An Unusual Case Report with Critical Appraisal of Existing Literature.颌骨中央巨细胞肉芽肿的治疗:一例罕见病例报告及对现有文献的批判性评价
Ann Maxillofac Surg. 2019 Jan-Jun;9(1):37-47. doi: 10.4103/ams.ams_232_18.
6
Non-odontogenic Intraosseous Radiolucent Lesions of the Mandibular Body Are Rare Findings on Panoramic Views of Patients With Neurofibromatosis Type 1.1型神经纤维瘤病患者全景片中,下颌骨体部非牙源性骨内透射性病变是罕见表现。
Anticancer Res. 2019 Apr;39(4):1971-1985. doi: 10.21873/anticanres.13308.
7
Cerebellar radiological abnormalities in children with neurofibromatosis type 1: part 1 - clinical and neuroimaging findings.1型神经纤维瘤病患儿的小脑影像学异常:第1部分 - 临床和神经影像学表现
Cerebellum Ataxias. 2018 Nov 1;5:14. doi: 10.1186/s40673-018-0093-y. eCollection 2018.
8
Cerebellar radiological abnormalities in children with neurofibromatosis type 1: part 2 - a neuroimaging natural history study with clinical correlations.1型神经纤维瘤病患儿的小脑影像学异常:第2部分——一项与临床相关的神经影像学自然史研究
Cerebellum Ataxias. 2018 Oct 30;5:13. doi: 10.1186/s40673-018-0092-z. eCollection 2018.
9
Craniofacial and oral alterations in patients with Neurofibromatosis 1.神经纤维瘤病 1 型患者的颅面和口腔改变。
Orphanet J Rare Dis. 2018 Aug 9;13(1):131. doi: 10.1186/s13023-018-0881-8.
10
Optic Pathway Glioma and Cerebral Focal Abnormal Signal Intensity in Patients with Neurofibromatosis Type 1: Characteristics, Treatment Choices and Follow-up in 134 Affected Individuals and a Brief Review of the Literature.1型神经纤维瘤病患者的视路胶质瘤与脑局灶性异常信号强度:134例患者的特征、治疗选择及随访并文献简要回顾
Anticancer Res. 2016 Aug;36(8):4095-121.