Sir,
Descemet's membrane detachment (DMD) was once a common occurrence during cataract surgery.1 Most peripheral and localized detachments resolve spontaneously.2 However, large and persistent detachments impair vision and require treatment.We report the successful attachment of DMD diagnosed 14 months after phacoemulsification.
Case report
A 65-year-old male presented to our centre, 14 months after uneventful phacoemulsification. A moderate postoperative visual gain was attributed by the primary surgeon to corneal oedema and was managed conservatively with topical steroids and antibiotics. Three months following surgery, topical acyclovir was added to the existing medication. There was no improvement even after more than 12 months of therapy.
On presentation to us, his best-corrected visual acuity was 20/125 in the right eye (RE) and 20/20 in the left eye (LE). Slit-lamp biomicroscopy revealed increased corneal thickness mostly distributed in the centre and inferior half of the cornea. The examination was remarkable for the absence of corneal vascularization, keratic precipitates, and cellular reaction in the anterior chamber. A shallow central Descemet's membrane detachment (DMD) was observed following instillation of 10% anhydrous glycerine (Figure 1a). It was continuous with the inferior side-port incision.
The DMD was successfully repaired with intracameral injection of perfluoropropane gas (14%). Corneal oedema resolved and visual acuity improved to 20/30 over a period of 7 days (Figure 1b). Confocal microscopy performed after re-attachment revealed an endothelial density of 1880 cells/mm2 in RE and 2112 cells/mm2 in the fellow pseudophakic eye (Figure 2a and b).
Comment
Localized, non-vision disturbing, DMD is not uncommon and tends to undergo spontaneous re-attachment.2 Larger DMDs present as a significant visual handicap.3, 4 Shah et al 5 reported successful attachment of late DMDs in three patients using perfluoropropane gas. In all three cases, the DMDs were detected 2–3 weeks after surgery. To the best of our knowledge, there is no published report on successful management of DMD diagnosed 14 months after surgery.
Our case highlights two important features. Firstly, DMD should be considered as a differential diagnosis for corneal oedema even in the late postoperative period. Secondly, despite a prolonged period of detachment, the DMD is amenable to surgical repair with good structural and functional outcome.
References
Aust W, Wernhard U . Defects of Descemet's membrane as a complication in cataract extraction with lens implantation. Dev Ophthalmol 1987; 13: 20–29.
Minkovitz JB, Schrenk LC, Pepose JS . Spontaneous resolution of an extensive detachment of Descemet's membrane following phacoemulsification. Arch Ophthalmol 1994; 112: 551–552.
Potter J, Zalatimo N . Descemet's membrane detachment after cataract extraction. Optometry 2005; 76: 720–724.
Mackool RJ, Holtz SJ . Descemet's membrane detachment. Arch Ophthalmol 1977; 95: 459–463.
Shah M, Bathia J, Kothari K . Repair of late Descemet's membrane detachment with perfluoropropane gas. J Cataract Refract Surg 2003; 29: 1242–1244.
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Vinekar, A., Sukhija, J., Brar, G. et al. ‘Late’ functionally successful repair of Descemet's membrane detachment following phacoemulsification. Eye 21, 555–556 (2007). https://doi.org/10.1038/sj.eye.6702638
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DOI: https://doi.org/10.1038/sj.eye.6702638