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Combined exfoliation and pigment dispersion: an overlap syndrome Mudumbai R; Liebmann JM; Ritch RTrans Am Ophthalmol Soc 1999[]; 97 (ä): 297-314; discussion 314-21PURPOSE: To describe a series of patients with combined pigment dispersion syndrome (PDS) and exfoliation syndrome (XFS) and to introduce a concept, the overlap syndrome, to aid in assessing multiple risk factors for glaucomatous damage. METHODS: A retrospective review of the records of all patients on our database who carried a diagnosis of both PDS/pigmentary glaucoma (PG) and XFS/exfoliative glaucoma (XFG). RESULTS: We identified 26 patients as having both XFS/XFG and PDS/PG. The average age was 64.3 +/- 9.8 years and 19 of 26 were men. All patients had bilateral PDS/PG. Bilateral XFS/XFG was present in 9 of 26 patients, and of the 17 patients with unilateral involvement, the left eye was affected in 13. CONCLUSION: Both XFS and PDS are common. Middle-aged patients with known PDS/PG should be suspected of having the onset of XFS if 1 eye escapes intraocular pressure control. Patients presenting with unilateral XFG may also have signs of PDS/PG, often remitted. We define an overlap syndrome as the appearance of a new co-morbidity for glaucomatous damage in a patient with a pre-existing risk factor, which then changes the course, and prognosis of the disease. This concept should be particularly useful in dealing with secondary and normal-tension glaucoma.|Exfoliation Syndrome/*complications/diagnosis[MESH]|Female[MESH]|Glaucoma, Open-Angle/etiology[MESH]|Humans[MESH]|Intraocular Pressure[MESH]|Iris/*pathology[MESH]|Male[MESH]|Middle Aged[MESH]|Pigment Epithelium of Eye/*pathology[MESH]|Prognosis[MESH]|Retrospective Studies[MESH]|Risk Factors[MESH] |
