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

Author:

Raccampo Luca1ORCID,Panozzo Giorgio2ORCID,Tel Alessandro1ORCID,Di Cosola Michele3,Colapinto Gianluca4,Trevisiol Lorenzo2ORCID,D’agostino Antonio2,Sembronio Salvatore1,Robiony Massimo1

Affiliation:

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

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

3. Section of Dentistry and Dental Prosthetics, Department of Medicine, University of Foggia, 71122 Foggia, Italy

4. Independent Researcher, 70121 Bari, Italy

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.

Publisher

MDPI AG

Subject

General Medicine

Reference115 articles.

1. Une cause rare de constriction permanente des machoires;Jacob;Bull. Mem. Soc. Anat. Paris,1899

2. Angeborene Kleinert der Unterkiefer;Langenbeck;Langenbecks Arch.,1861

3. Hyperplasia of the mandibular coronoid process: An analysis of 31 cases and a review of the literature;McLoughlin;J. Oral Maxillofac. Surg.,1995

4. Osteochondroma of the coronoid process (Jacob’s disease);Emekli;J. Oral Maxillofac. Surg.,2002

5. Osteochondroma of the Zygomatic Arch: A Case Report and Review of the Literature;Patel;J. Oral Maxillofac. Surg.,2018

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