An IDH1-mutated primary gliosarcoma: case report

Author:

Hsieh Jason K.12,Hong Christopher S.3,Manjila Sunil4,Cohen Mark L.5,Lo Simon167,Rogers Lisa168,Sloan Andrew E.146

Affiliation:

1. Case Western Reserve University School of Medicine, Cleveland;

2. Cleveland Clinic Lerner College of Medicine, Cleveland;

3. The Ohio State University School of Medicine, Columbus;

4. Department of Neurological Surgery, University Hospitals-Case Medical Center, Cleveland;

5. Department of Pathology, and

6. Case Comprehensive Cancer Center, Case Western Reserve University School of Medicine, Cleveland; and

7. Departments of Radiation Oncology and

8. Neurology, University Hospitals-Seidman Cancer Center, Cleveland, Ohio

Abstract

The authors present the case of a primary gliosarcoma with an isocitrate dehydrogenase-1 (IDH1) mutation. A 75-year-old man presented with a 3-day history of multiple focal seizures and was found on MRI to have a 2.2-cm left parietal enhancing mass lesion. Brain MRI for tremor performed 8 years prior to this presentation was normal. En bloc resection revealed a high-grade glioma with sarcomatous components that was immunoreactive for the R132H variant of IDH1 by antibody. Gliosarcoma is a rare variant of glioblastoma that arises most frequently as a primary tumor, and has equal or worse survival and an increased propensity for extracranial metastases compared with other Grade 4 gliomas. In contrast, isocitrate dehydrogenase-1 and -2 mutations are associated with low-grade gliomas with increased survival and less commonly with glioblastoma. To the authors' knowledge, there has been only 1 other published report of a primary gliosarcoma carrying an isocitrate dehydrogenase mutation. This rare genetic-histological combination highlights potential differences between glioblastoma and gliosarcoma and may warrant additional study.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

Genetics,Animal Science and Zoology

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