J Neurol Surg B Skull Base 2017; 78(S 01): S1-S156
DOI: 10.1055/s-0037-1600852
Poster Abstracts
Georg Thieme Verlag KG Stuttgart · New York

Primary Intracranial Gliosarcoma with Extensive Invasion of the Skull Base, Brain Parenchyma, Orbit, and Muscles of Mastication

Cody L. Nesvick
1   Mayo Clinic, Rochester, Minnesota, United States
,
Avital Perry
1   Mayo Clinic, Rochester, Minnesota, United States
,
Christopher S. Graffeo
1   Mayo Clinic, Rochester, Minnesota, United States
,
Quoc-Bao D. Nguyen
2   Texas A&M Health Science Center College of Medicine, Bryan, Texas, United States
,
Aditya Raghunathan
1   Mayo Clinic, Rochester, Minnesota, United States
,
Mark E. Jentoft
1   Mayo Clinic, Rochester, Minnesota, United States
,
Brian P. O'Neill
1   Mayo Clinic, Rochester, Minnesota, United States
,
Padraig P. Morris
1   Mayo Clinic, Rochester, Minnesota, United States
,
Jonathan M. Morris
1   Mayo Clinic, Rochester, Minnesota, United States
,
Jamie J. Van Gompel
1   Mayo Clinic, Rochester, Minnesota, United States
› Author Affiliations
Further Information

Publication History

Publication Date:
02 March 2017 (online)

 

Background: Gliosarcoma is an uncommon variant of glioblastoma, which commonly demonstrates dural attachment. However, skull base invasion has is very rarely seen with this entity. We report the first case of a primary intracranial gliosarcoma extensively invading the skull base extracranial compartments including muscles of mastication.

Methods: Case report.

Results: A 44-year-old woman presented to our institution with a three-month history of difficult right jaw opening and retro-orbital pressure, and one week of severe right-sided post-auricular headache. Head CT demonstrated a 6-cm mass with marked bony erosion; Brain MRI at a one-week interval more clearly characterized tumor extension through the right orbit and muscles of mastication, with overall growth to 7-cm and worsening midline shift. The patient underwent a right frontotemporal craniotomy for gross total resection. Pathology confirmed the diagnosis of gliosarcoma, IDH-wildtype (WHO grade IV). Her postoperative course was uneventful and she was discharged at preoperative neurologic baseline.

Conclusion: To our knowledge, this is the first reported case of a primary intracranial gliosarcoma with direct invasion of skull base, brain parenchyma, and extracranial compartment, including temporal bone and surrounding musculature. This case report highlights the rapid aggressiveness of gliosarcomas, and further a prior undescribed radiographic and anatomic finding of skull base invasion with this entity.

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