An early presentation of osteochondroma: a rare case
Rahul Agola, Parth Shah
Corresponding author: Rahul Agola, Department of Orthopaedics, Datta Meghe Institute of Medical Sciences, Wardha, Maharashtra, India
Received: 30 Jul 2022 - Accepted: 01 Sep 2022 - Published: 02 Sep 2022
Domain: Pediatric oncology, Orthopedic surgery
Keywords: Osteochondroma, benign, bone tumor, childhood
©Rahul Agola et al. PAMJ Clinical Medicine (ISSN: 2707-2797). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Cite this article: Rahul Agola et al. An early presentation of osteochondroma: a rare case. PAMJ Clinical Medicine. 2022;10:2. [doi: 10.11604/pamj-cm.2022.10.2.36582]
Available online at: https://www.clinical-medicine.panafrican-med-journal.com//content/article/10/2/full
An early presentation of osteochondroma: a rare case
&Corresponding author
The most prevalent benign bone tumor, osteochondroma, accounts for 30 to 35% of all benign bone tumors. It most frequently affects teenagers and young adults, with a 1 in 50,000 incidence rate. Osteochondroma only has a 1% chance of developing into a malignant condition like chondrosarcoma. Osteochondroma has an autosomal dominant pattern, and prehypertrophic chondrocytes in the growth plate are affected by the EXT gene mutation. Osteochondroma patients typically have their knee joint affected and typically report painless swelling around major joints. These swellings result from the long bone's metaphysis's excessive development of cartilage and bone. This swelling could result in mechanical symptoms like compression of the neurovascular system. The mother of a 3-year-old kid brought him to the orthopaedics outpatient department with complaints of painless swelling in the right wrist, left scapula, and left ankle that had been reported two months prior. Her 5-year-old sibling has a similar, painless swelling that is only modest in size. The patient is being handled conservatively and recommended to keep regular follow-ups every three months because they currently have no additional complaints. The state and prognosis of the disease have been disclosed to the patient's parents. Operative management needs to wait till the skeleton is fully developed.
Figure 1: child with early presentation of osteochondroma with X-ray; (A) circular swelling coming from the left scapula's lateral surface; (B) swelling on the forearm's distal end; (C) multiple osteochondroma suggestive changes in both lower limb; (D) metaphysical growth from distal end radius