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Washington University Experience | NEOPLASMS (EMBRYONAL) | ATRT - Atypical Teratoid Rhabdoid Tumor | 8A1 ATRT (Case 8) H&E 2X
Case 8 History ---- The patient was a two year old male with a large, enhancing mass with necrosis in the frontal lobe and both lateral ventricles. Operative procedure: Craniotomy for tumor resection. ---- 8A1-6 This is a high grade neoplasm with multifocal necrosis and various morphologies. In some areas, the tumor is composed of sheets of polygonal cells with eccentric nuclei and abundant eosinophilic cytoplasm, imparting a rhabdoid appearance. However, in other areas, the neoplastic cells have oval or elongated hyperchromatic nuclei and indistinct or spindled cytoplasmic processes reminiscent of astrocytes. Other spindled areas appear more mesenchymal and are arranged in intersecting bundled elements with a myxomatous background and mimic chordoma (8A1, arrow). Mitotic figures are readily found.
