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雅各布病:病例系列、广泛文献综述及分类建议

Jacob's Disease: Case Series, Extensive Literature Review and Classification Proposal.

作者信息

Raccampo Luca, Panozzo Giorgio, Tel Alessandro, Di Cosola Michele, Colapinto Gianluca, Trevisiol Lorenzo, D'agostino Antonio, Sembronio Salvatore, Robiony Massimo

机构信息

Maxillofacial Surgery Department, Academic Hospital of Udine, Department of Medicine, University of Udine, 33100 Udine, Italy.

Section of Oral and Maxillofacial Surgery, Department of Surgical Sciences, Dentistry, Gynaecology and Paediatrics, University of Verona, 37129 Verona, Italy.

出版信息

J Clin Med. 2023 Jan 25;12(3):938. doi: 10.3390/jcm12030938.

Abstract

Jacob's disease is a rare entity consisting of the formation of a pseudojoint between an abnormal coronoid process of the mandible and the inner surface of the zygomatic bone. First described by Jacob in 1899, its diagnosis and definition have never been entirely univocal. In this paper, we present three emblematic cases and an extensive review of the literature on Jacob's disease. Given the variability observed in the presentation of the disease, we have developed a proposal for the classification, here reported.

摘要

雅各布病是一种罕见病症,表现为下颌骨异常喙突与颧骨内表面之间形成假关节。1899年由雅各布首次描述,其诊断和定义从未完全明确。在本文中,我们展示了三个典型病例,并对有关雅各布病的文献进行了全面综述。鉴于该疾病临床表现的多样性,我们制定了一种分类方案,在此报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a6f/9917974/dcf3cefd4a8f/jcm-12-00938-g001.jpg

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