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. 2022 Sep;34(5):898-901.
doi: 10.1177/10406387221107898. Epub 2022 Jun 27.

OLIG2 immunolabeling in feline ependymoma

Affiliations

OLIG2 immunolabeling in feline ependymoma

Elena A Demeter et al. J Vet Diagn Invest. 2022 Sep.

Abstract

Ependymoma, one of the most common gliomas in cats, occurs most often in the lateral and third ventricles and has variable histologic patterns that often form rosettes and pseudorosettes. Oligodendrocyte transcription factor (OLIG2) is expressed in oligodendrocyte precursor cells and mature oligodendrocytes. Although widely used as a diagnostic marker for most gliomas, OLIG2 is reported to have minimal immunolabeling in ependymomas. Here we characterize the OLIG2 immunolabeling pattern in 19 cases of feline ependymoma, which occurred predominantly in the lateral and third ventricles. Immunohistochemistry for GFAP was variable in 14 cases and was typically localized in the cytoplasmic processes of the neoplastic ependymal cells, especially in the rosettes and pseudorosettes. Nuclear OLIG2 immunolabeling was present in 17 cases and varied in intensity from weak (4 cases) to strong (13 cases). The distribution of OLIG2 immunolabeling within the neoplasms included none (2 cases), <25% (7 cases), 25-50% (6 cases), 51-75% (2 cases), and >75% (3 cases). OLIG2 immunolabeling intensity and distribution is widespread in feline ependymoma, in contrast to ependymomas in other species, and should not be relied upon as a specific marker for feline oligodendroglioma.

Keywords: OLIG2; ependymoma; feline; glioma; neuropathology.

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Conflict of interest statement

Declaration of conflicting interests: The authors declare no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Figures

Figures 1-6.
Figures 1-6.
Feline ependymoma. Figure 1. Classic feline ependymoma with prominent pseudorosettes and cords of neoplastic ependymal cells; case 3. H&E. Figure 2. Abundant cytoplasmic GFAP immunolabeling of neoplastic ependymal cells forming the pseudorosettes; case 19. Figure 3. OLIG2 immunolabeling is absent in the neoplastic cells; case 14. Figure 4. Weak intranuclear OLIG2 immunolabeling in <25% of the neoplastic cells; case 16. Figure 5. Strong intranuclear OLIG2 immunolabeling in 25–50% of the neoplastic cells; case 7. Figure 6. Strong intranuclear OLIG2 immunolabeling in >75% of the neoplastic cells; case 3.

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Supplementary concepts