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Article
September 1991

Poorly Differentiated Primary Orbital Sarcoma (Presumed Malignant Rhabdoid Tumor)Radiologic and Histopathologic Correlation

Author Affiliations

From the Neuro-Ophthalmology Division, Mason Institute of Ophthalmology, University of Missouri-Columbia (Dr Johnson); and the Departments of Pathology (Dr Sexton) and Ophthalmology (Dr Goldberg), Penn State University, Hershey, Pa. Dr Sexton is now with the University of Florida, Gainesville.

Arch Ophthalmol. 1991;109(9):1275-1278. doi:10.1001/archopht.1991.01080090101031
Abstract

• A 47-year-old man presented with acquired hyperopia and gaze-evoked visual loss. Computed tomography and magnetic resonance imaging demonstrated a well-circumscribed intraconal tumor. Histopathologic studies indicated that the tumor was a poorly differentiated primary orbital sarcoma compatible with malignant fibrous histiocytoma or malignant rhabdoid tumor. To our knowledge, no case of primary orbital malignant rhabdoid tumor has been previously described in an adult.

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