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AJNR Awards, New Junior Editors, and more. Read the latest AJNR updates

Case of the Month

Section Editor: Nicholas Stence, MD
Children's Hospital Colorado, Aurora, CO

Submit a Case Previous Cases

April 2014
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Next Case of the Month coming May 6 . . .

Gliosarcoma

  • Gliosarcoma (GSM) is a rare primary CNS neoplasm with reported incidence of 1–8% of all the malignant gliomas. This is a highly vascular tumour exhibiting marked tumor angiogenesis and slight temporal lobes preponderance.
  • Secondary gliosarcoma refers to sarcomatous change in a pre-existent or partially resected/treated glioma.
  • No significant differences are seen with GSM and glioblastoma.
  • GSM can invade meninges and bone. It can metastasize to other body parts.
  • Key Diagnostic Features: GSM is known to present with lobar hemorrhage and can mimic a vascular malformation. If an angiogram is obtained, network of blood vessels and early venous shunting is seen. The extensive vascular nature of the lesion results in increased perfusion. Otherwise, on conventional imaging, the lesion can look similar to glioblastoma. The pathologist remains the final arbiter.
  • DDx: Glioblastoma, metastasis
  • Rx: Surgical excision/debulking and radiation-chemotherapy
  • Prognosis: Very poor

Suggested Reading

  1. Jack Jr CR, Bhansali DT, Chason JL, et al. Angiographic features of gliosarcoma. AJNR Am J Neuroradiol 1987;8:117–22
  2. Zhang B-Y, Hong C, Geng D-Y, et al. Computed tomography and magnetic resonance features of gliosarcoma: a study of 54 cases. J Comput Assist Tomogr 2011;35:667–73, 10.1097/RCT.0b013e3182331128
  3. Kozak KR, Mahadevan A, Moody JS. Adult gliosarcoma: epidemiology, natural history, and factors associated with outcome. Neuro Oncol 2009;11:183–91, 10.1215/15228517-2008-076

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American Journal of Neuroradiology: 46 (7)
American Journal of Neuroradiology
Vol. 46, Issue 7
1 Jul 2025
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