CASE REPORT |
|
Year : 2020 | Volume
: 11
| Issue : 2 | Page : 62-68 |
|
Coronoid Hyperplasia (Jacob’s Disease) as a Rare Cause of Restricted Mouth Opening: a Case Report
Mohammad Hasan Samandari1, Milad Etemadi Shalamzari1, Maryam Ghazizadeh2, Hooman Navaei3
1 Department of Oral and Maxillofacial Surgery, Dental Implant Research Center, School of Dentistry, Isfahan University of Medical Science, Isfahan, Iran 2 Department of Oral and Maxillofacial Radiology, School of Dentistry, Kermanshah University of Medical Science, Kermanshah, Iran 3 Department of Oral and Maxillofacial Surgery, School of Dentistry, Isfahan University of Medical Science, Isfahan, Iran
Correspondence Address:
Assistant Professor Maryam Ghazizadeh Department of Oral and Maxillofacial Radiology, School of Dentistry, Kermanshah University of Medical sciences, Kermanshah Iran
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/denthyp.denthyp_61_19
|
|
Introduction: Restricted mouth opening (MO) is associated with the problems in intra/extra-articular components such as trauma to the articular bone component especially at the early ages, chronic displacement of the articular disk, tumors, condylar anomalies, coronoid hyperplasia and hyperactivity of jaw muscles. A pseudo-joint can form between the zygoma and the hyperplastic coronoid process (Jacob’s disease). Pseudo-joint restricts MO, it causes multiple problems for patients, and finally it decreases the quality of their or patients’ lives. Therefore, early diagnosis and treatment are very important. Case Report: Described here is a 28-year-old man that due to trauma in childhood, his coronoid process became hyperplastic. The pseudo-joint formed between coronoid process and zygomatic bone interfere with MO. Discussion: The intraoral approach offers direct access without the risk of facial nerve injury or scars on the face
|
|
|
|
[FULL TEXT] [PDF]* |
|
 |
|