A case of subretinal neovascularization treated with intravitreal ranibizumab in a patient with idiopathic juxtafoveal retinal telangiectasis
Clinical Interventions in Aging downloaded from https://www.dovepress.com/ by 37.59.46.207 on 13-Jul-2018
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C A S E R E P O RT
A case of subretinal neovascularization treated
with intravitreal ranibizumab in a patient
with idiopathic juxtafoveal retinal telangiectasis
Dimitrios Karagiannis 1
Ilias Georgalas 2
Ioannis Ladas 2
Parikakis Eustratios 1
Panagiotis Mitropoulos 1
Second Department of
Ophthalmiatrion Eye Hospital ,NHS,
Athens, Greece; 2 Department of
Ophthalmology, “G.Genimatas”
General Hospital, Athens, Greece
1
Abstract: A 65-year-old lady presented with decreased vision in her left eye (LE). Best corrected
visual acuity (BCVA) was 1/20. Complete examination showed idiopathic juxtafoveal retinal
telangiectasis associated with subretinal neovascularization and she was treated with intravitreal
ranibizumab every month for three months in the LE. After four months, her BCVA increased to
3/10. Fluorescein angiography (FA) showed minimal leakage and optical coherence tomography
(OCT) confirmed absence of intra- or subretinal fluid in the macula. Examinations were repeated
monthly for another 12 months and showed no recurrence. Intravitreal ranibizumab showed
promising results for subretinal neovascularization due to idiopathic juxtafoveal retinal telangiectasis. A prospective study with large series of patients and controls may be necessary in
order to determine the effectiveness of this treatment.
Keywords: idiopathic juxtafoveal retinal telangiectasis, ranibizumab, subretinal
neovascularization
Introduction
Gass and Blodi1 defined bilateral acquired retinal telangiectasis or perifoveal telangiectasia or type 2A telangiectasis as a rare retinal disease characterized by retinal
thickening temporal to the fovea, right-angle venules, retinal pigment epithelial (RPE)
hyperplastic plaques, and crystalline deposits. Bilateral acquired retinal telangiectasis
can be divided into five stages. The disease is usually becoming symptomatic through
the sixth decade of life when complicated by subretinal neovascularization which is
localized mostly subfoveally in stage 5 of the disease.1–3
We report the outcome of treatment with 0.5 mg intravitreal ranibizumab in a
patient with a subretinal neovascular membrane secondary to idiopathic juxtafoveal
retinal telangiectasis.
Case history
Correspondence: Ilias Georgalas
Consultant Ophthalmic Surgeon,
59 Chrysanthemon Str., Psychico 15452,
Athens, Greece
Tel +30 21 0776 8374
Fax +30 21 0776 8374
Email
A 65-year-old Caucasian lady presented to our clinic complaining of decreased vision
in her left eye (LE). On presentation, best-corrected visual acuity (BCVA) was 10/10
in the right eye (RE) and 1/20 LE. Anterior segment examination was unremarkable in
both eyes and intraocular pressures were within normal limits. Fundus biomicroscopy
revealed in the right macula, slightly dilated right-angle veins with RPE hyperplasia
beneath them (Figure 1A). In addition to these findings, in the left macula there was
subretinal hemorrhage (Figure 1B). The clinical appearance of the macular area
of the LE was consistent with idiopathic juxtafoveal retinal telangiectasis complicated by subretinal neovascularization. Fluorescein angiography (FA) and optical
coherence tomography (OCT) were performed and confirmed the above diagnosis
(Figures 1C–D, 2, 3A). OCT of the LE revealed the characteristic appearance of outer
and inner retina having similar reflectivity and an area temporal to the fovea with high
Clinical Interventions in Aging 2009:4 63–65
63
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Clinical Interventions in Aging downloaded from https://www.dovepress.com/ by 37.59.46.207 on 13-Jul-2018
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Karagiannis et al
Figure 1A) Right eye: Color fundus picture showing slightly dilated right-angle
veins with retinal pigment epithelium hyperplasia beneath them. B) Left eye: Color
fundus picture showing subretinal hemorrhage inferior and temporal to the fovea.
C) Venous phase of FA of the LE depicts early hyperfluorescence corresponding to
the neovascular membrane and hypofluorescence inferior to the membrane corresponding to the subretinal hemorrhage. D) Late phase of FA showing leakage from
the neovascular membrane.
Figure 2 Oblique section of OCT of the LE.
Abbreviations: LE, left eye; OCT, optical coherence tomography.
Abbreviations: FA, fluorescein angiography; LE, left eye; OCT, optical
coherence tomography.
reflectivity corresponding to the temporal area of choroidal
neovascularization (CNV) (Figure 3A), which was observed
in the angiogram. After a discussion outlining the possible
risks and benefits of the treatment, the patient was started
on 0.5 mg intravitreal ranibizumab in the LE. Based on the
findings of FA and OCT which were performed monthly, the
patient underwent three intravitreal injections of ranibizumab
every month for three months. Following these injections,
BCVA increased to 3/10 and both clinical and angiographic
appearances showed significant improvement with minimal
leakage in FA and absence of intra- or subretinal fluid in
OCT and significant reduction in retinal thickness; the RPE
remained thickened (Figures 3B, 4A–B). Examinations
were repeated monthly for another 12 months and showed
no recurrence of CNV.
Figure 3A) Oblique section of OCT of the LE revealing the characteristic
appearance of outer and inner retina having similar reflectivity and an area temporal
to the fovea with high reflectivity corresponding to the temporal area of choroidal
neovascularization observed in the angiogram. B) OCT of the same section of LE
revealing significant reduction in retinal thickness. The RPE remains thickened.
Abbreviations: LE, left eye; OCT, optical coherence tomography; RPE, retinal
pigment epithelium.
near the fovea and visible telangiectasis only in FA.
In stage 3, FA shows capillary dilatation and staining.
Stage 4 reveals migrating RPE cells appearing as stellate
foci along the right-angle venules. Stage 5, according to
Gass and Blodi, or the proliferative stage according to
Discussion
Bilateral acquired retinal telangiectasis or retinal
telangiectasis type 2A, according to Gass and Blodi,
or type 2 perifoveal telangiectasia according to the
classification by Yannuzzi is a symmetrical disease.1,3
The area involved is usually less than a disc diameter
and is typically temporal to the fovea.1 Gas and Blodi
divided the development of group 2A telangiectasis into
five stages.1 Stage 1 is found on FA on the asymptomatic
fellow eye as staining at the level of the RPE. Stage 2
is characterized by the loss of transparency of the retina
64
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Figure 4 A) Left eye: Color fundus picture following ranibizumab treatment revealing significant improvement with no subretinal hemorrhag (...truncated)