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Solitary Osteochondroma of the Scapula in a Young Male: A Case Report
INTRODUCTION: Osteochondroma is a type of cartilaginous tumor. It is the most common benign tumor of axial skeleton usually arising around the knee, proximal humerus, and pelvis. Solitary osteochondroma of the scapula is relatively rare and usually incidental finding accompanied by pain and dysfunct...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Indian Orthopaedic Research Group
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826679/ https://www.ncbi.nlm.nih.gov/pubmed/36659891 http://dx.doi.org/10.13107/jocr.2022.v12.i07.2906 |
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author | Jindal, Vasu Khandekar, Anil Gupta, Parag Binyala, Shrey |
author_facet | Jindal, Vasu Khandekar, Anil Gupta, Parag Binyala, Shrey |
author_sort | Jindal, Vasu |
collection | PubMed |
description | INTRODUCTION: Osteochondroma is a type of cartilaginous tumor. It is the most common benign tumor of axial skeleton usually arising around the knee, proximal humerus, and pelvis. Solitary osteochondroma of the scapula is relatively rare and usually incidental finding accompanied by pain and dysfunction. These lesions can easily be followed radiographically with plain radiograph. Computed tomography (CT) is used to determine the precise location and its relationship with the surrounding soft tissues and enable accurate surgical removal. CASE REPORT: In this report, we present a rare case of a symptomatic scapular osteochondroma in a 18-year-old male who presented with the complaints of swelling over the left scapula. X-ray showed a bony outgrowth along the posteromedial border of the left scapula. CT scan was done to know extent of the growth. MRI was performed to rule out soft-tissue involvement. Despite the young age of the patient, surgical excision was performed. The outcome was good, the patient noticed disappearance of swelling and a normal profile of the scapula was gained. CONCLUSION: We have described a rare case of scapular osteochondroma associated with different signs, symptoms, and positive radiological findings. This lesion was removed surgically, and a follow-up indicated complete symptom relief with no history of recurrence. By reporting this case, we aim to increase the awareness of unusual manifestations of osteochondroma, particularly in terms of site, age of onset, and atypical presenting signs and symptoms. |
format | Online Article Text |
id | pubmed-9826679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Indian Orthopaedic Research Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-98266792023-01-18 Solitary Osteochondroma of the Scapula in a Young Male: A Case Report Jindal, Vasu Khandekar, Anil Gupta, Parag Binyala, Shrey J Orthop Case Rep Case Report INTRODUCTION: Osteochondroma is a type of cartilaginous tumor. It is the most common benign tumor of axial skeleton usually arising around the knee, proximal humerus, and pelvis. Solitary osteochondroma of the scapula is relatively rare and usually incidental finding accompanied by pain and dysfunction. These lesions can easily be followed radiographically with plain radiograph. Computed tomography (CT) is used to determine the precise location and its relationship with the surrounding soft tissues and enable accurate surgical removal. CASE REPORT: In this report, we present a rare case of a symptomatic scapular osteochondroma in a 18-year-old male who presented with the complaints of swelling over the left scapula. X-ray showed a bony outgrowth along the posteromedial border of the left scapula. CT scan was done to know extent of the growth. MRI was performed to rule out soft-tissue involvement. Despite the young age of the patient, surgical excision was performed. The outcome was good, the patient noticed disappearance of swelling and a normal profile of the scapula was gained. CONCLUSION: We have described a rare case of scapular osteochondroma associated with different signs, symptoms, and positive radiological findings. This lesion was removed surgically, and a follow-up indicated complete symptom relief with no history of recurrence. By reporting this case, we aim to increase the awareness of unusual manifestations of osteochondroma, particularly in terms of site, age of onset, and atypical presenting signs and symptoms. Indian Orthopaedic Research Group 2022-07 2022-07 /pmc/articles/PMC9826679/ /pubmed/36659891 http://dx.doi.org/10.13107/jocr.2022.v12.i07.2906 Text en Copyright: © Indian Orthopaedic Research Group https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Jindal, Vasu Khandekar, Anil Gupta, Parag Binyala, Shrey Solitary Osteochondroma of the Scapula in a Young Male: A Case Report |
title | Solitary Osteochondroma of the Scapula in a Young Male: A Case Report |
title_full | Solitary Osteochondroma of the Scapula in a Young Male: A Case Report |
title_fullStr | Solitary Osteochondroma of the Scapula in a Young Male: A Case Report |
title_full_unstemmed | Solitary Osteochondroma of the Scapula in a Young Male: A Case Report |
title_short | Solitary Osteochondroma of the Scapula in a Young Male: A Case Report |
title_sort | solitary osteochondroma of the scapula in a young male: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826679/ https://www.ncbi.nlm.nih.gov/pubmed/36659891 http://dx.doi.org/10.13107/jocr.2022.v12.i07.2906 |
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