Surgical Treatment of Jacob’s Disease: A Case Report Involving an Osteochondroma of the Coronoid Process
Although it is one of the most common benign tumors of bone in the axial skeleton, the osteochondroma is relatively rare in the maxillofacial region. Its discovery on the coronoid process is even more rare. First described by Jacob in 1899, it remains a rare entity as only a few reported cases have...
Saved in:
Main Authors: | , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2013-01-01
|
Series: | Case Reports in Surgery |
Online Access: | http://dx.doi.org/10.1155/2013/253740 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832552215669112832 |
---|---|
author | Dale E. Stringer Kourt B. Chatelain Rahul Tandon |
author_facet | Dale E. Stringer Kourt B. Chatelain Rahul Tandon |
author_sort | Dale E. Stringer |
collection | DOAJ |
description | Although it is one of the most common benign tumors of bone in the axial skeleton, the osteochondroma is relatively rare in the maxillofacial region. Its discovery on the coronoid process is even more rare. First described by Jacob in 1899, it remains a rare entity as only a few reported cases have been described in the literature. Nevertheless, the symptomatic features remain relatively nonspecific: limited opening, tightness, and slight expansion of the affected area with or without pain. The demographic features are more established, as it affects younger males. Definitive diagnosis is made after histological analysis, post-resection of the growth. We report a 27 year-old male with a history of limited opening and tightness of the mouth. Computed Tomography (CT) imaging revealed a well corticated exophytic protuberance from the left coronoid process. Left coronoidectomy and excision of the exophytic growth was performed, and was confirmed by histologic analysis to be an osteochondroma, demonstrating Jacob’s disease. |
format | Article |
id | doaj-art-386ea490945143d6abfc57b11f0a3f21 |
institution | Kabale University |
issn | 2090-6900 2090-6919 |
language | English |
publishDate | 2013-01-01 |
publisher | Wiley |
record_format | Article |
series | Case Reports in Surgery |
spelling | doaj-art-386ea490945143d6abfc57b11f0a3f212025-02-03T05:59:09ZengWileyCase Reports in Surgery2090-69002090-69192013-01-01201310.1155/2013/253740253740Surgical Treatment of Jacob’s Disease: A Case Report Involving an Osteochondroma of the Coronoid ProcessDale E. Stringer0Kourt B. Chatelain1Rahul Tandon2Department of Oral and Maxillofacial Surgery, Loma Linda University, Loma Linda, CA 92350, USADepartment of Oral and Maxillofacial Surgery, Loma Linda University, Loma Linda, CA 92350, USADepartment of Oral and Maxillofacial Surgery, Loma Linda University, Loma Linda, CA 92350, USAAlthough it is one of the most common benign tumors of bone in the axial skeleton, the osteochondroma is relatively rare in the maxillofacial region. Its discovery on the coronoid process is even more rare. First described by Jacob in 1899, it remains a rare entity as only a few reported cases have been described in the literature. Nevertheless, the symptomatic features remain relatively nonspecific: limited opening, tightness, and slight expansion of the affected area with or without pain. The demographic features are more established, as it affects younger males. Definitive diagnosis is made after histological analysis, post-resection of the growth. We report a 27 year-old male with a history of limited opening and tightness of the mouth. Computed Tomography (CT) imaging revealed a well corticated exophytic protuberance from the left coronoid process. Left coronoidectomy and excision of the exophytic growth was performed, and was confirmed by histologic analysis to be an osteochondroma, demonstrating Jacob’s disease.http://dx.doi.org/10.1155/2013/253740 |
spellingShingle | Dale E. Stringer Kourt B. Chatelain Rahul Tandon Surgical Treatment of Jacob’s Disease: A Case Report Involving an Osteochondroma of the Coronoid Process Case Reports in Surgery |
title | Surgical Treatment of Jacob’s Disease: A Case Report Involving an Osteochondroma of the Coronoid Process |
title_full | Surgical Treatment of Jacob’s Disease: A Case Report Involving an Osteochondroma of the Coronoid Process |
title_fullStr | Surgical Treatment of Jacob’s Disease: A Case Report Involving an Osteochondroma of the Coronoid Process |
title_full_unstemmed | Surgical Treatment of Jacob’s Disease: A Case Report Involving an Osteochondroma of the Coronoid Process |
title_short | Surgical Treatment of Jacob’s Disease: A Case Report Involving an Osteochondroma of the Coronoid Process |
title_sort | surgical treatment of jacob s disease a case report involving an osteochondroma of the coronoid process |
url | http://dx.doi.org/10.1155/2013/253740 |
work_keys_str_mv | AT daleestringer surgicaltreatmentofjacobsdiseaseacasereportinvolvinganosteochondromaofthecoronoidprocess AT kourtbchatelain surgicaltreatmentofjacobsdiseaseacasereportinvolvinganosteochondromaofthecoronoidprocess AT rahultandon surgicaltreatmentofjacobsdiseaseacasereportinvolvinganosteochondromaofthecoronoidprocess |