PURPOSE: To describe the spectral-domain optical coherence tomography features in a patient with an atypical presentation of hypotonous maculopathy after successful retinal detachment surgery. METHODS: A 64-year-old man underwent scleral buckling with pars plana vitrectomy for the repair of retinal detachment. Postoperatively, the retina was attached but he had poor recovery of vision. Intraocular pressure was recorded to be on the lower side of normal. He underwent posterior segment evaluation by spectral-domain optical coherence tomography. RESULTS: Spectral-domain optical coherence tomography revealed cystoid macular edema and a neurosensory detachment involving the posterior pole. In addition, underneath the neurosensory detachment, spectral-domain optical coherence tomography revealed folds of the retinal pigment epithelium and Bruch membrane, features of hypotonous maculopathy. CONCLUSION: Spectral-domain optical coherence tomography is a useful investigational modality in the diagnosis of ocular hypotony presenting with atypical features.
PURPOSE: To describe the spectral-domain optical coherence tomography features in a patient with an atypical presentation of hypotonous maculopathy after successful retinal detachment surgery. METHODS: A 64-year-old man underwent scleral buckling with pars plana vitrectomy for the repair of retinal detachment. Postoperatively, the retina was attached but he had poor recovery of vision. Intraocular pressure was recorded to be on the lower side of normal. He underwent posterior segment evaluation by spectral-domain optical coherence tomography. RESULTS: Spectral-domain optical coherence tomography revealed cystoid macular edema and a neurosensory detachment involving the posterior pole. In addition, underneath the neurosensory detachment, spectral-domain optical coherence tomography revealed folds of the retinal pigment epithelium and Bruch membrane, features of hypotonous maculopathy. CONCLUSION: Spectral-domain optical coherence tomography is a useful investigational modality in the diagnosis of ocular hypotony presenting with atypical features.