Journal of Orthopedics and Joint Surgery

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VOLUME 5 , ISSUE 1 ( January-June, 2023 ) > List of Articles

CASE REPORT

Osteochondroma at Unusual Sites: A Case Series Report

Ashok Ramanujam, Annamalai Devadoss, Sathish Devadoss, Jayakumar Subbiah, Deepak Chithragar, Balaji Rajendran

Keywords : Benign bone tumor, Capitellum, Exostosis, Osteochondroma, Primary bone tumors, Ribs, Talus, Unusual sites

Citation Information : Ramanujam A, Devadoss A, Devadoss S, Subbiah J, Chithragar D, Rajendran B. Osteochondroma at Unusual Sites: A Case Series Report. 2023; 5 (1):30-32.

DOI: 10.5005/jp-journals-10079-1106

License: CC BY-NC 4.0

Published Online: 03-01-2023

Copyright Statement:  Copyright © 2023; The Author(s).


Abstract

Osteochondroma, the most common benign bone tumor, involves 10–15% of all bone tumors. It can occur frequently either as solitary osteocartilaginous exostosis or rarely as hereditary multiple lesions. The most common sites of occurrence are long bones of the lower arm (50%), usually the lower end of the femur and upper end of the tibia. However, involvement of the small hand and foot bones occurs in 10% of cases, pelvis in 5%, scapulae in 4%, and spine in 2%. Symptoms are not very specific. The authors present a case series of atypical sites of osteochondroma. In the present case series report, we describe a case series of osteochondroma arising from the talus, trochlea, and ribs, respectively.


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  1. Calafiore G1, Calafiore G, Bertone C, et al. [Osteochondroma. Report of a case with atypical localization and symptomatology]. Acta Bio-medica de L'ateneo Parmense: Organo Della Societa di Medicina e Scienze Naturali di Parma 2001;72(5–6):91–96. PMID: 12233271.
  2. Chrisman OD, Goldenberg RR. Untreated solitary osteochondroma. Report of two cases. J Bone Joint Surg Am 1968;50(3):508–512. DOI: 10.2106/00004623-196850030-00009
  3. Kitsoulis P, Galani V, Stefanaki K, et al. Osteochondromas: review of the clinical, radiological and pathological features. In Vivo 2008;22(5):633–646. PMID: 18853760.
  4. Tepelenis K, Papathanakos G, Kitsouli A, et al. Osteochondromas: an updated review of epidemiology, pathogenesis, clinical presentation, radiological features and treatment options. In Vivo 2021;35(2):681–691. DOI: 10.21873/invivo.12308
  5. Garcia RA, Inwards CY, Unni KK. Benign bone tumors—recent developments. Semin Diagn Pathol 2011;28(1):73–85. DOI: 10.1053/j.semdp.2011.02.013
  6. Saglik Y, Altay M, Unal VS, et al. Manifestations and management of osteochondromas: a retrospective analysis of 382 patients. Acta Orthop Belg 2006;72(6):748–755. PMID: 17260614.
  7. Schmale GA, Conrad EU, Raskind WH. The natural history of hereditary multiple exostoses. J Bone Joint Surg Am 1994;6(7):986–992. DOI: 10.2106/00004623-199407000-00005
  8. Gordon SL, Buchanan JR, Ladda RL. Hereditary multiple exostoses: report of a kindred. J Med Genet 1981;18(6):428–430. DOI: 10.1136/jmg.18.6.428
  9. Lee KCY, Davies AM, Cassar-Pullicino VN. Imaging the complications of osteochondromas. Clin Radiol 2002;57(1):18–28. DOI: 10.1053/crad.2001.0719
  10. Suranigi S, Rengasamy K, Najimudeen S, et al. Extensive osteochondroma of talus presenting as tarsal tunnel syndrome: report of a case and literature review. Arch Bone Jt Surg 2016;4(3):269–272. PMCID: PMC4969376; PMID: 27517075.
  11. Shariatzadeh H, Jafari D, Taheri H, et al. Intra-articular osteochondroma of the elbow: a case report. J Shoulder Elbow Surg 2010;19(3):e1–e4. DOI: 10.1016/j.jse.2009.09.013
  12. Maeda K, Watanabe T, Sato K, et al. Two cases of asymptomatic rib exostosis treated by prophylactic surgical excision. J Pediatr Surg Case Reports 2017;20:24–28. DOI: 10.1016/j.epsc.2017.03.004
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