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July 1972

Pathological Condition of the Retinal Pigment EpitheliumNeoplasms and Nodular Non-neoplastic Lesions

Author Affiliations

USA, Washington, DC; New Haven, Conn
From the Registry of Ophthalmic Pathology, Armed Forces Institute of Pathology, and the Department of Ophthalmology, the George Washington University Medical Center, Washington, DC (Dr. Tso), and the Section of Ophthalmology, Yale University School of Medicine, New Haven, Conn (Dr. Albert).

Arch Ophthalmol. 1972;88(1):27-38. doi:10.1001/archopht.1972.01000030029007

Eleven primary neoplasms of the retinal pigment epithelium (RPE) were studied histopathologically. These tumors presented a variety of histologic patterns, namely mosaic, tubular, papillary, or a patternless arrangement of vacuolated or anaplastic cells. The tumor with the mosaic pattern was regarded as best differentiated, the anaplastic tumor the least differentiated, and the tumors with vacuolated cells or tubular or papillary patterns in the middle of the spectrum. Such tumors invaded the retina and choroid, but metastasis was not observed. These neoplasms were contrasted with six nodular reactive proliferations of RPE, one of which approached neoplasia. Histologic criteria for differentiation of neoplasia from reactive proliferation are discussed. The available clinical data on tumors of the RPE and on reactive lesions are analyzed and compared.

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