Osteochondroma of the Proximal Tibia in a 12-Year-Old Male: A Case Report

Case Report

Authors

  • Fachrizal Arfani Prawiragara Faculty of Medicine, Universitas Pembangunan Nasional Veteran Jawa Timur, Surabaya, Indonesia
  • Leonardo Tedjaprasadja Faculty of Medicine, Universitas Pembangunan Nasional Veteran Jawa Timur, Surabaya, Indonesia

DOI:

https://doi.org/10.55175/cdk.v53i08.2057

Keywords:

Case report, osteochondroma, pediatric bone tumor, proximal tibia, skeletal immaturity

Abstract

Introduction: Osteochondroma is the most common benign bone tumor, commonly occurring in the metaphyseal region of long bones during the second and third decades of life. Although frequently asymptomatic, osteochondroma arising from the proximal tibia in a skeletally immature patient is uncommon and may present challenges due to its proximity to the growth plate. This case highlights the diagnostic and surgical considerations in pediatric patient required to preserve skeletal growth while achieving complete tumor removal. Case: A 12-yearold boy presented with a painless swelling over the proximal region of the right tibia that had progressively developed over two months. Physical examination revealed a firm, immobile bony mass measuring approximately 2 × 2.5 cm, no tenderness and without neurovascular impairment. Radiographic evaluation demonstrated a pedunculated osteochondroma with continuity of the cortex and medulla with the host bone, showing growth away from the epiphysis and a positive neck sign. Surgical excision was performed with careful preservation of surrounding neurovascular structures. Histopathological examination confirmed the diagnosis of conventional osteochondroma without malignant features. Conclusion: This case represents an uncommon presentation of proximal tibial osteochondroma in a skeletally immature patient. Early recognition, appropriate imaging assessment, and meticulous surgical planning are essential to prevent complications and maintain normal limb function. At follow-up, the patient showed no recurrence and returned to normal activities.

Downloads

Download data is not yet available.

References

Fowler J, Takayanagi A, Fiani B, Cathel A, Sarhadi KJ, Arshad M, et al. Diagnosis, management, and treatment options: a cervical spine osteochondroma meta-analysis. World Neurosurg. 2021;149:215–25.e6. doi: 10.1016/j.wneu.2021.01.148.

Luo Z, Ye C, Sang HX. Osteosarcoma in the coracoid process that mimicked an osteochondroma: a case report. Medicine (Baltimore). 2017;96(46):e8608. doi: 10.1097/MD.0000000000008608.

Veeravagu A, Li A, Shuer LM, Desai AM. Cervical osteochondroma causing myelopathy in adults: management considerations and literature review. World Neurosurg. 2017;97:752.e5–752.e13. doi: 10.1016/j.wneu.2016.10.061.

Wu JS, Hochman MG. Bone tumors: a practical guide to imaging. German (Berlin): Springer; 2012.

Tong K, Liu H, Wang X, Zhong Z, Cao S, Zhong X, et al. Osteochondroma: review of 431 patients from one medical institution in South China. J Bone Oncol. 2017;30:23–9. doi: 10.1016/j.jbo.2017.08.002.

Kushner BH, Roberts SS, Friedman DN, Kuk D, Ostrovnaya I, Modak S, et al. Osteochondroma in long-term survivors of high-risk neuroblastoma. Cancer. 2015;121:2090–6. doi: 10.1002/cncr.29316.

Raswan US, Bhat AR, Tanki H, Samoon N, Kirmani AR. A solitary osteochondroma of the cervical spine: a case report and review of literature. Childs Nerv Syst. 2017;33(6):1019–22. doi: 10.1007/s00381-017-3394-1.

Lin GX, Wu HJ, Chen CM, Rui G, Hu BS. Osteochondroma arising from the inferior articular process of the lumbar spine in a geriatric patient: a case report and literature review. Geriatr Orthop Surg Rehabil. 2022;13:21514593211073028. doi: 10.1177/21514593211073028.

Hakim DN, Pelly T, Kulendran M, Caris JA. Benign tumours of the bone: a review. J Bone Oncol. 2015;4(2):37–41. doi: 10.1016/j.jbo.2015.02.001.

Ali S, Kaplan S, Kaufman T, Fenerty S, Kozin S, Zlotolow DA. Madelung deformity and Madelung-type deformities: a review of the clinical and radiological characteristics. Pediatr Radiol. 2015;45(12):1856–63. doi: 10.1007/s00247-015-3390-0.

Tepelenis K, Papathanakos G, Kitsouli A, Troupis T, Barbouti A, Vlachos K, et al. Osteochondromas: an updated review of epidemiology, pathogenesis, clinical presentation, radiological features and treatment options. In Vivo. 2021;35(2):681–91. doi: 10.21873/invivo.12308.

Gavanier M, Blum A. Imaging of benign complications of exostoses of the shoulder, pelvic girdles and appendicular skeleton. Diagn Interv Imaging. 2017;98(1):21–8. doi: 10.1016/j.diii.2015.11.021.

Hari A, Kavar B. Rare case of malignant transformation of a solitary spinal osteochondroma into recurrent metastatic chondrosarcoma. J Clin Neurosci. 2019;67:280–8. doi: 10.1016/j.jocn.2019.05.045.

Joshi G, Bhatta OP, Chand H, Mudbhari B, Dangol N, Bhetwal P. A solitary osteochondroma of the sixth cervical spine: A case report. Int J Surg Case Rep. 2023;110:108729. doi: 10.1016/j.ijscr.2023.108729.

Yakkanti R, Onyekwelu I, Carreon LY, Dimar JR II. Solitary osteochondroma of the spine: a case series and review of solitary osteochondroma with myelopathic symptoms. Global Spine J. 2018;8(4):323–39. doi: 10.1177/2192568217701096.

Downloads

Published

15-08-2026

How to Cite

Prawiragara, F. A., & Tedjaprasadja, L. (2026). Osteochondroma of the Proximal Tibia in a 12-Year-Old Male: A Case Report: Case Report. Cermin Dunia Kedokteran, 53(08), 542–546. https://doi.org/10.55175/cdk.v53i08.2057