Abstract

BackgroundInternal limiting membrane (ILM) drape sign is an important OCT characteristic of Macular telangiectasia type 2 (MacTel 2). Described here is a case where masking of the ILM drape sign occurred with bilateral foveal detachments in a patient with MacTel 2.Case presentationA 64-year old female was diagnosed with MacTel 2, four years prior to the current presentation on the basis of an OCT demonstrating bilateral ILM drape sign. Fluorescein angiography showed bilateral dilated, ectatic capillaries and late phase dye leak. At the current presentation there was bilateral gradual visual impairment over two months due to bilateral foveal detachments. Treatment with intravitreal Bevacizumab resulted in unmasking of the pre-existing ILM drape sign at 12 weeks. Visual acuity was reduced to counting fingers in the left eye with the neovascular membrane as a consequence of sub-retinal fibrosis, while the right eye maintained a vision of 6/12. A difference in the stage of the disease at presentation determined the long-term visual outcome after seven years of observation.ConclusionFoveal detachment can influence the OCT detectability of pre-existing foveal cystoid lesions. Visual prognosis at the final follow up was consistent with the interocular disparity of the disease stage at presentation.

Highlights

  • Internal limiting membrane (ILM) drape sign is an important Optical coherence tomography (OCT) characteristic of Macular telangiectasia type 2 (MacTel 2)

  • It is well recognised that OCT has allowed the detection of a wide range of foveal signs in MacTel not previously identified with other diagnostic modalities

  • An additional diagnosis of left subretinal neovascularization (SRNV) was made on the basis of a half a disc diameter area of sub-retinal hemorrhage temporal to the foveola at three weeks follow-up as shown in Fig. 3 (a,b)

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Summary

Introduction

Internal limiting membrane (ILM) drape sign is an important OCT characteristic of Macular telangiectasia type 2 (MacTel 2). Conclusion: Foveal detachment can influence the OCT detectability of pre-existing foveal cystoid lesions. In a population of 310 patients, Clemons et al described OCT signs in 74% of eyes, which included apparent foveal detachment, inner/outer photoreceptor segment breaks, hyper-reflectivity or loss of the outer nuclear layer, intra-retinal pigment migration, subretinal neovascularization (SRNV)/fibrosis, and foveal cystoid lesions of the inner retinal layers [3].

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