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颧弓骨软骨瘤:一例报告并文献复习

Osteochondroma of the Zygomatic Arch: A Case Report and Review of the Literature.

作者信息

Patel Ryan, Obeid George

机构信息

Department of Oral and Maxillofacial Surgery, MedStar Washington Hospital Center, Washington, DC.

Department of Oral and Maxillofacial Surgery, MedStar Washington Hospital Center, Washington, DC.

出版信息

J Oral Maxillofac Surg. 2018 Sep;76(9):1912-1916. doi: 10.1016/j.joms.2018.03.038. Epub 2018 Mar 31.

DOI:10.1016/j.joms.2018.03.038
PMID:29684307
Abstract

An osteochondroma, when reported in the maxillofacial region, is a benign neoplasm that involves the skull base, maxillary sinus, zygomatic arch, or mandible. Most commonly, the osteochondroma occurs in the coronoid process and the condyle. One rare subtype of osteochondroma reported in the literature, termed Jacob disease, arises from the coronoid process and interferes with the zygomatic arch. This report describes a unique case of an isolated osteochondroma arising from the zygomatic arch and interfering with the coronoid process, which was treated through surgical excision by an intraoral approach. The literature search indicated that this is 1 among only 9 other reported cases since 1964 in which an osteochondroma arose primarily from the zygomatic arch.

摘要

骨软骨瘤发生于颌面部时,是一种累及颅底、上颌窦、颧弓或下颌骨的良性肿瘤。最常见的是,骨软骨瘤发生于冠状突和髁突。文献中报道的一种罕见的骨软骨瘤亚型,称为雅各布病,起源于冠状突并累及颧弓。本报告描述了一例独特的孤立性骨软骨瘤,起源于颧弓并累及冠状突,通过口内入路手术切除进行治疗。文献检索表明,自1964年以来,这是仅有的9例其他报道病例中的1例,其中骨软骨瘤主要起源于颧弓。

相似文献

1
Osteochondroma of the Zygomatic Arch: A Case Report and Review of the Literature.颧弓骨软骨瘤:一例报告并文献复习
J Oral Maxillofac Surg. 2018 Sep;76(9):1912-1916. doi: 10.1016/j.joms.2018.03.038. Epub 2018 Mar 31.
2
Osteochondroma of the right coronoid process (Jacob disease): a case report.右冠突骨软骨瘤(雅各布病):一例报告
Cranio. 2013 Jan;31(1):66-9. doi: 10.1179/crn.2013.010.
3
Joint formation between an osteochondroma of the coronoid process and the zygomatic arch (Jacob disease): report of case and review of literature.冠状突骨软骨瘤与颧弓之间的关节形成(雅各布病):病例报告及文献复习
J Oral Maxillofac Surg. 2000 Feb;58(2):227-32. doi: 10.1016/s0278-2391(00)90345-8.
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Ann Ital Chir. 2015 Nov 3;86:S2239253X15024408.
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Sarcomatous transformation of osteochondroma of the coronoid process forming pseudoarthrosis with zygomatic arch mistaken for Jacob disease.冠状突骨软骨瘤的肉瘤样转变形成假关节并与颧弓相连,误诊为雅各布病。
J Craniofac Surg. 2014;25(2):e101-2. doi: 10.1097/SCS.0000000000000409.
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Coronoid osteochondroma of the mandible: transzygomatic access and autogenous bony reconstruction.下颌骨喙突骨软骨瘤:经颧弓入路及自体骨重建
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A case report of osteochondroma of the frontotemporosphenoidal suture.额颞蝶缝骨软骨瘤病例报告
J Exp Clin Cancer Res. 2004 Mar;23(1):147-51.
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One-stage treatment to osteochondroma of the coronoid process and secondary facial asymmetry with coronoidectomy and reduction malarplasty: a case report and literature review.一期治疗冠状突骨软骨瘤及继发面部不对称的冠状突切除术和颧骨复位成形术:病例报告及文献综述
J Oral Maxillofac Surg. 2014 Sep;72(9):1870.e1-1870.e13. doi: 10.1016/j.joms.2014.04.030. Epub 2014 May 5.
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Imaging and histopathological features of Jacob's disease: a case study.雅各布病的影像学和组织病理学特征:一项病例研究。
Head Neck Pathol. 2012 Mar;6(1):51-3. doi: 10.1007/s12105-011-0324-5. Epub 2011 Dec 22.
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Transzygomatic coronoidectomy through an extended coronal incision for treatment of trismus due to an osteochondroma of the coronoid process of the mandible.通过延长冠状切口行颧弓下喙突切除术治疗下颌骨喙突骨软骨瘤所致牙关紧闭
Ann Plast Surg. 1998 Oct;41(4):425-9. doi: 10.1097/00000637-199810000-00014.

引用本文的文献

1
Osteochondroma of the condyle of the mandible: A case report.下颌骨髁突骨软骨瘤:一例报告。
Natl J Maxillofac Surg. 2025 Jan-Apr;16(1):174-179. doi: 10.4103/njms.njms_137_23. Epub 2025 Apr 28.
2
Osteochondroma below the Infraorbital Rim - A Case Report.眶下缘下方骨软骨瘤——病例报告
Ann Maxillofac Surg. 2024 Jul-Dec;14(2):232-235. doi: 10.4103/ams.ams_199_23. Epub 2024 Aug 30.
3
Jacob's Disease: Case Series, Extensive Literature Review and Classification Proposal.雅各布病:病例系列、广泛文献综述及分类建议
J Clin Med. 2023 Jan 25;12(3):938. doi: 10.3390/jcm12030938.
4
Zygomatico-Coronoid Pseudoarthrosis Due to Osteochandroma of Coronoid Process: A Rare Entity.由于冠状突骨软骨瘤导致的颧突-冠状突假关节:一种罕见病例。
Iran J Otorhinolaryngol. 2021 May;33(116):183-186. doi: 10.22038/ijorl.2021.48888.2617.