A Case Of Mac Tel 2 With An Unusual Sub Macular Vitelliform Lesion

A Case Of Mac Tel 2 With An Unusual Sub Macular Vitelliform Lesion

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  A case ofMac Tel 2 with an unusual sub macular vitelliform lesion DR RENUKA SARWATE DR LEKHA T Divyadrishti Lasers, Satara.
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  INTRODUCTION  Macular telangiectasia(Mac Tel 2) or Idiopathic Para Foveal Telangiectasia (PFT) is recognized as a primary neuroretinal degenerative condition with secondary vascular involvement.  It is bilateral symmetrical disease characterized by telangiectasias, refractile deposits in the superficial retina, hyperpigmented RPE plaques and subretinal neovascularization.  Rarely small, round yellow lesions may be seen in the fovea mimicking the vitelliform lesions in Adult onset foveo macular dystrophy(AFMD)  A 71-year-old healthy woman presented to our hospital in September 2010 with a referral diagnosis of choroidal neovascularization (CNV) in the RE
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  On examination RE : LE BCVA6/12 6/9 Fundus Yellowish sub macular lesion of one third disc diameter in size Retinal pigment epithelial(RPE) depigmentation and minimal telangiectasia parafoveally FFA ill defined hyperflourescence subfoveally Temporal parafoveal leakage OCT Subfoveal hyper reflective clump of echoes, discontinuity of the ellipsoid line (IS/OS layer) with intact RPE. Foveal thinning with CFT of 180 microns, multiple lamellar holes, break in the IS/OS layer and intact RPE
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   Figure 1:Fundus photograph at presentation showing sub macular yellowish lesion, one-third disc diameter in size, not associatedwith any vascular changes, pigmentation or CNV in the RE (a), RPE hypo pigmentation over fovea with minimal graying and telangiectasia in the LE (b).  Fluorescein angiography showing ill defined hyper fluorescence sub foveally in the RE (c) and temporal parafoveal leakage in the LE (d).  Spectral domain Optical Coherence Tomography (OCT) of the RE showing hyper reflective clump of echoes sub foveally, normal morphology of all the retinal layers around the lesion and no features of CNV (e). In the LE there is foveal thinning, small sub foveal lamellar hole and internal limiting membrane (ILM) drape with disruption of outer retinal layers temporally (f). Disruption of the ellipsoid line and intact RPE are noted in BE
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   On subsequentvisits her ERG,EOG normal in both eyes.  Arden’s ratio 2.7 in RE and 4.3 in LE.  By December 2011, her BCVA had reduced to 6/24 in the RE and 6/12 in the LE.  Fundus and OCT remained unchanged in the RE, but LE showed increased RPE depigmentation and pigmented plaque along the dilated venule
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   Figure 2:At 15 months follow up the sub retinal lesion in the RE remaining unchanged on fundus (a) and OCT (c)  LE fundus showing increased parafoveal RPE depigmentation and a small pigmented plaque along the right angled venule temporally.  OCT of the LE showing multiple lamellar holes sub foveally increased disruption of the outer retinal layers with hyper reflective echoes temporally suggestive of progression (d).  MfERG recording (e) showing normal response in the RE and diminished amplitudes in the inner rings I n the LE.
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  DISCUSSION  Mac Tel2 is often under diagnosed in the early stages due to subtle fundus changes or misdiagnosed in the late stages as age related macular degeneration resulting in inappropriate treatment.  Yellowish foveal lesion first documented by Gass in eyes with PFT can be mistaken clinically for AFMD.  The OCT features of such lesions include hyper reflective mound of material between the ellipsoid region and RPE with irregular reflectivity and focal loss of the overlying photoreceptor layer and outer limiting membrane .  AFMD is also characterized by similar hyper reflective subretinal lesions resulting from shed photoreceptor outer segments
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   In AFMDthere is obvious reaction to the material with RPE hypertrophy, hyper pigmentation or anterior migration whereas in PFT, RPE remains as a monolayer with minimal reaction, probably due to defective muller cell function.  Full field ERG may be normal in both but mfERG is reduced in the macula and in the periphery in AFMD indicating widespread RPE abnormality
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   Our patientwith typical PFT in the LE showed natural progression over 3 years, whereas the subretinal lesion in the RE remained unchanged both clinically and on OCT.  Based on the analysis of a single eye it is difficult to comment whether such subretinal debris is masking the typical findings or it actually prevening the progression of PFT.
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