Suboccipital osteoblastoma: Microsurgical resection of a rare entity

2Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

Background: Osteoblastomas are rare lesions comprising 1% of all bone tumors. The occipital bone is one of the rarest affected bone, with only 11 cases reported during the last 40 years. Case Description: Here, we describe the clinical presentation and the radiological features of a suboccipital osteoblastoma that was successfully resected in a 30-year-old man. A short video shows the microsurgical removal of the lesion. There was no recurrence during a 12-month follow-up. Conclusions: Even if osteoblastomas are benign tumors, a complete removal has to be achieved to reduce the risk of recurrences. This makes necessary an appropriate monitoring of the patient.

Cite

CITATION STYLE

APA

Choque-Velasquez, J., Colasanti, R., Piippo, A., & Niemelä, M. (2017). Suboccipital osteoblastoma: Microsurgical resection of a rare entity. Surgical Neurology International, 8(1). https://doi.org/10.4103/sni.sni_444_16

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free