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J GlaucomaMarch 20200 citations

Solitary Free-Floating Iris Cyst Associated With Bilateral Pigment Dispersion Syndrome: Report of a Case.

Bruttini Carlo, Vulpetti Andrea, Riva Ivano, Katsanos Andreas, Oddone Francesco, Quaranta Luciano


AI Summary

This case reports a free-floating iris cyst in a patient with pigment dispersion syndrome. The key finding is this unique association, suggesting a possible link between PDS and dislodged iris pigment cysts, which may influence glaucoma management.

Abstract

Case report: A 27-year-old white man with a 5-year history of pigment dispersion syndrome presented for evaluation. His past ocular history was significant for bilateral intraocular pressure elevation that had required intraocular pressure -lowering medication (beta-blocker-prostaglandin analogue fixed combination). On ophthalmic examination, the visual acuity was 20/20 without correction in both eyes. Anterior chamber slit-lamp examination revealed a pigmented round mass with modest transillumination at 6-o'clock position of the right eye. When asked, the patient reported that he had first noticed a shadow in his right eye during childhood when he was flexing his neck and keeping a face-down position for a few seconds. During a head-flexing test, the mass freely floated in the anterior chamber. When the patient extended the neck, the round mass could be seen in front of the pupil. After a few moments, the mass would slowly fall to the iridocorneal angle at the 6-o'clock position. Ultrasound biomicroscopy and anterior-segment optical coherence tomography confirmed that the lesion was a pigmented cyst without internal reflectivity. Specular microscopy examinations, performed to exclude cyst-induced corneal endothelium compromise, revealed a cell-density of ~3000 cells/mm in both eyes. Gonioscopy showed an open angle with trabecular pigmentation and funduscopy a cup-to-disc ratio of 0.5 bilaterally. Visual fields and optical coherence tomography tests were within normal limits.

Conclusions

The etiology of free-floating iris cysts is unclear, but it is generally agreed that these masses are usually dislodged pigment epithelial cysts. This is the first report of a unilateral free-floating iris cyst associated with bilateral pigment dispersion syndrome.


MeSH Terms

AdultAnterior ChamberCystsGlaucoma, Open-AngleGonioscopyHumansIntraocular PressureIris DiseasesMaleMicroscopy, AcousticSlit Lamp MicroscopyTomography, Optical CoherenceTonometry, OcularVisual Acuity

Key Concepts6

This is the first report of a unilateral free-floating iris cyst associated with bilateral pigment dispersion syndrome.

EpidemiologyCase seriesCase Reportn=1 patient

A 27-year-old white man with a 5-year history of pigment dispersion syndrome presented with bilateral intraocular pressure elevation that required intraocular pressure-lowering medication (beta-blocker-prostaglandin analogue fixed combination).

DiagnosisCase seriesCase Reportn=1 patientCh28

Anterior chamber slit-lamp examination of a 27-year-old white man with pigment dispersion syndrome revealed a pigmented round mass with modest transillumination at the 6-o'clock position of the right eye, which freely floated in the anterior chamber during a head-flexing test.

DiagnosisCase seriesCase Reportn=1 patientCh4

Ultrasound biomicroscopy and anterior-segment optical coherence tomography confirmed that the lesion in the right eye of a 27-year-old white man with pigment dispersion syndrome was a pigmented cyst without internal reflectivity.

DiagnosisCase seriesCase Reportn=1 patientCh4

Specular microscopy examinations performed on a 27-year-old white man with a free-floating iris cyst and bilateral pigment dispersion syndrome revealed a corneal endothelial cell-density of ~3000 cells/mm in both eyes.

DiagnosisCase seriesCase Reportn=1 patientCh4

Gonioscopy showed an open angle with trabecular pigmentation and funduscopy revealed a cup-to-disc ratio of 0.5 bilaterally in a 27-year-old white man with a free-floating iris cyst and bilateral pigment dispersion syndrome.

DiagnosisCase seriesCase Reportn=1 patientCh4Ch5

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