Juxtapapillary Retinal Pigment Epithelial Tumor
- 1 March 1971
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Ophthalmology (1950)
- Vol. 85 (3), 299-301
- https://doi.org/10.1001/archopht.1971.00990050301010
Abstract
ADENOCARCINOMAS of the retinal pigment epithelium are among the rarest of intraocular tumors.1,2 They are usually diagnosed by the pathologist after the eye has been enucleated as a suspected malignant melanoma or because of unrelated ocular abnormalities, and must be differentiated from the more common focal mass produced by reactive hyperplasia of the retinal pigment epithelium which is often initiated by trauma or focal inflammation. The histologic differentiation of true neoplasms from reactive hyperplasias of the retinal pigment epithelium is often difficult to discern; even for experienced pathologists.2,3 The report of a case which follows exemplifies this difficulty. Report of a Case A 26-year-old white man was seen by an optometrist on Oct 2, 1969, with complaints of decreased right visual acuity and a superior-temporal visual field defect. An intraocular mass was visualized and the patient referred to the ophthalmology clinic. Five years prior to admission, the patientKeywords
This publication has 2 references indexed in Scilit:
- VAGARIES OF THE RETINAL PIGMENT EPITHELIUMInternational Ophthalmology Clinics, 1962
- Tumors of the Retinal Pigment Epithelium*American Journal of Ophthalmology, 1958