Gliosarcoma associated with bilateral hippocampal sclerosis in a cat presenting complex partial seizures with orofacial involvement: A case report

Author:

Martinez Ana1ORCID,Binks Sophie2,Pumarola Martí3,Hardas Alexandros4,Easton Alistair5,Campo Leticia5,Browne Molly5,Martins Susana5,Garosi Laurent S.6,Di Dona Francesco7,Tauro Anna89ORCID

Affiliation:

1. Queen's Veterinary School University of Cambridge Cambridge UK

2. Oxford Autoimmune Neurology Group University of Oxford Oxford UK

3. Mouse and Comparative Pathology Unit, Department of Animal Medicine and Surgery, Veterinary Faculty, Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER‐BBN), Campus UAB Universitat Autònoma de Barcelona Barcelona Spain

4. Department of Pathobiology and Population Sciences The Royal Veterinary College Hatfield UK

5. Translational Histopathology Laboratory, Department of Oncology University of Oxford Oxford UK

6. Vet Oracle Teleradiology, CVS Limited Norfolk UK

7. Freelance Consultant Naples Italy

8. Chestergates Veterinary Specialists, Units E&F Chester UK

9. College of Veterinary Medicine North Carolina State University Raleigh North Carolina USA

Abstract

Key Clinical MessageGliosarcoma, a rare cerebral neoplasm, has not been linked to hippocampal changes in cats. We report a case of complex partial seizures with orofacial involvement, revealing gliosarcoma concurrent with bilateral hippocampal sclerosis.AbstractA 16‐year‐old neutered female domestic shorthair cat presented with acute inappetence, ataxia, disorientation, and vacant staring. Brain MRI revealed an ill‐defined, round, intra‐axial mass in the right piriform lobe, showing hyperintensity on T2W, T2‐FLAIR, and T2*W, and hypointensity on T1W images. The lesion exhibited mass effect and contrast enhancement in its center. Bilateral hyperintensity on T2‐FLAIR images and contrast enhancement were observed in the hippocampus. Brain histologic and immunohistochemical analysis revealed cerebral gliosarcoma with concurrent hippocampal sclerosis. Feline LGI1‐antibody testing on the serum and/or CSF was not performed due to insufficient biomaterial. Although retrospective testing on brain tissue was considered, it ultimately proved unfeasible, preventing us from ruling out antibody‐associated limbic encephalitis. In conclusion, cerebral gliosarcoma should be included in feline intracranial tumor differentials, warranting brain MRI and feline LGI1‐antibody testing in cats showing complex partial seizures with orofacial involvement. In our case, the prognosis remained poor due to the presence of a high‐grade glioma.

Publisher

Wiley

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