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C2 Osteoblastoma: Rare Presentation and Management Review

Received: 26 December 2018    Accepted: 21 January 2019    Published: 3 September 2019
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Abstract

Osteoblastoma is a rare and benign osteoid producing primary bone tumor that affect mainly the long bones. Spine account for thirty-six percent of these tumor. The mean age of presentation was 20 years, with a range of 6 months to 75 years. We report about a 12-year-old male child who presented with neck pain. Radiology revealed C2 osteoblatoma. Whole mass was removed in to No recurrence was seen at 1 year follow up. In conclusion, case delineates the difficulty of delayed diagnosis, the challenges and surgical management and also the favourable prognosis.

Published in American Journal of Pediatrics (Volume 5, Issue 3)
DOI 10.11648/j.ajp.20190503.26
Page(s) 175-177
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Osteoblastoma, Neck Pain, Cervical

References
[1] Amirjamshidi A, Abbassioun K: Osteoblastoma of the third cervical vertebra in a 16-year-old boy: case report and review of the literature. Pediatr Neurosurg 2010, 46 (5): 396–401.
[2] Yilmaz C, Civelek E, Caner H, Aydin AE, Gerilmez A, Altinors N. Osteoblastoma of C2 corpus: 4 year follow up. Asian spine journl. 6: 2012; 136-139.
[3] Zileli M, Cagli S, Basdemir G, Ersahin Y. Osteoid 
osteomas and osteoblastomas of the spine. Neurosurg 
Focus 2003; 15: E5.
[4] Koc K, IIik MK. Surgical management of an osteoblastoma involving the entire C2 vertebra and review of literature. Eur Spine J. 2016 May; 25 Suppl 1: 220-3.
[5] Deutsch H, Haid RW, Rodts GE, Mummaneni PV: Post laminectomy cervical deformity. Neurosurg Focus 2003; 15 (3): E5.
[6] Albert TJ, Vacarro A. Postlaminectomy kyphosis. Spine (Phila Pa 1976) 1998; 23 (24): 2738-27454.Zileli M, Cagli S, Basdemir G, Ersahin Y. Osteoid osteomas and osteoblastomas of the spine. Neurosurgical Focus. 2003; 15: E5.
[7] Combalia Aleu A, Popescu D, Pomes J, Palacin A. Long standing pain in a 25- year old patient with a non-diagnosed cervical osteoblastoma: a case report. Arch Orthopaedic Trauma Surg 2008; 128: 567-71.
[8] Camitta B, Wells R, Segura A, Unni KK, Murray K, Dunn D. Osteoblastoma response to chemotherapy. Cancer 1991; 68: 999-1003.
[9] Bhargava P,Singh R,Garg BB. Dorsal spine osteoblastoma. Asian J Neurosurg. 2016; 11 (2): 180-182.
[10] .Rajasekaran S, Kama RM, Kamath V, Shetty AP. Computer navigation-guided excision of cervical osteoblastoma.Eur Spine J. 2010; 19: 1046-1047.
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  • APA Style

    Uday Singh Raswan, Aishwarya Aditya Mehra. (2019). C2 Osteoblastoma: Rare Presentation and Management Review. American Journal of Pediatrics, 5(3), 175-177. https://doi.org/10.11648/j.ajp.20190503.26

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    ACS Style

    Uday Singh Raswan; Aishwarya Aditya Mehra. C2 Osteoblastoma: Rare Presentation and Management Review. Am. J. Pediatr. 2019, 5(3), 175-177. doi: 10.11648/j.ajp.20190503.26

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    AMA Style

    Uday Singh Raswan, Aishwarya Aditya Mehra. C2 Osteoblastoma: Rare Presentation and Management Review. Am J Pediatr. 2019;5(3):175-177. doi: 10.11648/j.ajp.20190503.26

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  • @article{10.11648/j.ajp.20190503.26,
      author = {Uday Singh Raswan and Aishwarya Aditya Mehra},
      title = {C2 Osteoblastoma: Rare Presentation and Management Review},
      journal = {American Journal of Pediatrics},
      volume = {5},
      number = {3},
      pages = {175-177},
      doi = {10.11648/j.ajp.20190503.26},
      url = {https://doi.org/10.11648/j.ajp.20190503.26},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajp.20190503.26},
      abstract = {Osteoblastoma is a rare and benign osteoid producing primary bone tumor that affect mainly the long bones. Spine account for thirty-six percent of these tumor. The mean age of presentation was 20 years, with a range of 6 months to 75 years. We report about a 12-year-old male child who presented with neck pain. Radiology revealed C2 osteoblatoma. Whole mass was removed in to No recurrence was seen at 1 year follow up. In conclusion, case delineates the difficulty of delayed diagnosis, the challenges and surgical management and also the favourable prognosis.},
     year = {2019}
    }
    

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Author Information
  • Department of Neurosurgery, Amandeep Hospital, Amritsar, India

  • Department of Neurosurgery, Amandeep Hospital, Amritsar, India

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