Combined Oligodendroglioma/Pleomorphic Xanthoastrocytoma: A Probable Collision Tumor: Case Report

Author:

Perry Arie1,Scheithauer Bernd W.2,Szczesniak David M.3,Atkinson John L.D.4,Wald John T.3,Hammak Julie E.5

Affiliation:

1. Division of Neuropathology Washington University School of Medicine, St. Louis, Missouri

2. Divisions of Neuropathology Mayo Clinic, Rochester, Minnesota

3. Neurosurgery Mayo Clinic, Rochester, Minnesota

4. Neuroradiology Mayo Clinic, Rochester, Minnesota

5. Neuro-Oncology Mayo Clinic, Rochester, Minnesota

Abstract

Abstract OBJECTIVE AND IMPORTANCE We report the first case of combined oligodendroglioma and pleomorphic xanthoastrocytoma. CLINICAL PRESENTATION A female college student and competitive cross-country runner presented to the Mayo Clinic at age 18 years with complaints of progressive headache and visual disturbances. Neuroimaging revealed a heavily calcified left parieto-occipital mass with focal enhancement and remodeling of the overlying calvarium. INTERVENTION A histological examination of the nearly gross total resection specimen disclosed a low-grade oligodendroglioma discretely abutting a superficially situated focus of pleomorphic xanthoastrocytoma. Ten months thereafter, a recurrence was suspected on the basis of the detection of a new focus of nodular enhancement. This lesion stabilized after radiation therapy, and the patient is well, without apparent residual disease 2.8 years after surgery. CONCLUSION This unique neoplasm is presumed to represent a collision tumor, its biological behavior being similar to that of oligodendroglioma alone. However, the possibility of an unusual, mixed oligoastrocytoma with pleomorphic xanthoastrocytoma as the astrocytic component cannot be excluded entirely. Potentially, both components have the capacity for recurrence and anaplastic transformation.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Clinical Neurology,Surgery

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