Pigmentary retinal dystrophy associated with pigmentary glaucoma

• Published in: Graefe's archive for clinical and experimental ophthalmology Vol. 227; no. 4; p. 335
• Main Authors: Piccolino, F C, Calabria, G, Polizzi, A, Fioretto, M
• Format: Journal Article
• Language: English
• Published: Germany 01.01.1989
• Subjects: Adult; Fundus Oculi; Glaucoma, Open-Angle - complications; Humans; Intraocular Pressure; Laser Therapy; Male; Neovascularization, Pathologic - complications; Pigment Epithelium of Eye - pathology; Retina - blood supply; Retinal Degeneration - complications; Retinal Detachment - complications; Retinal Detachment - surgery; Visual Acuity; Visual Field Tests
• ISSN: 0721-832X
• DOI: 10.1007/BF02169408

Two young brothers were bilaterally affected by pigmentary glaucoma and extensive symmetrical changes of the retinal pigment epithelium (RPE). Fundus changes consisted in widespread salt-and-pepper RPE mottling and pigment clumping, sparing only the peripapillary and foveal areas. During the course of 4 years, one of the two patients suffered multiple, recurrent, exudative and hemorrhagic detachments of the RPE that involved the midperiphery and posterior pole. No exudative lesions appeared in the brother. The medical history and systemic laboratory tests were noncontributory in both patients. The ERG was normal and the EOG subnormal. Dark adaptation was delayed and showed an elevation of the scotopic threshold. These cases seem to support the hypothesis that the RPE is also involved in the pigmentary dispersion syndrome. An inherited defect could affect the pigment epithelium in both the anterior and posterior segments of the eye. The multifocal subretinal exudative pattern that occurred in one of our patients has not been previously observed in hereditary disorders of the RPE.