Abstract
Immunohistochemical and molecular biologic techniques have done much to advance our understanding of many CNS and non-CNS tumors. Unfortunately, there is no reliable immunohistochemical stain for neoplastic oligodendroglial cells, and recent advances in the molecular biology of these tumors have not yet been parlayed into the diagnostic armementarium of practicing pathologists. Therefore, the oligodendroglioma currently remains a tumor whose diagnosis is based entirely on the “good old H&E.” In addition, we have been provided with a variety of look-alikes serving to constantly challenge, and more than occasionally, humble us. While some of these rather uncommon “oligo-mimics” will be covered below, our usual challenge is separating oligodendroglial tumors from those of astrocytic lineage (1). This is particularly important for three reasons:
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1.
Oligodendroglial tumors, particularly the high-grade ones, respond well to a variety chemotherapeutic regimens, while astrocytic tumors generally do not (2).
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2.
Exclusive of this chemoresponsiveness, oligodendrogliomas are biologically less aggressive than astrocytomas of similar grade.
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3.
Due to their relatively high cellularity, the failure to recognize low-grade oligodendroglial tumors generally leads to diagnoses of high-grade astrocytomas, resulting in unnecessary therapeutic interventions which may cause significant morbidity.
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Prayson, R.A., Cohen, M.L. (2000). Oligodendroglioma. In: Practical Differential Diagnosis in Surgical Neuropathology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-037-7_10
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DOI: https://doi.org/10.1007/978-1-59259-037-7_10
Publisher Name: Humana Press, Totowa, NJ
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