Features Associated With Foveal Retinal Detachment in Myopic Macular Retinoschisis




Purpose


To determine the retinal features seen on enhanced spectral-domain optical coherence tomography (SD-OCT) associated with foveal retinal detachment in eyes with myopic macular retinoschisis.


Design


Retrospective case series.


Methods


We reviewed fundus photographs and conventional and enhanced SD-OCT images of 21 eyes of 19 patients with myopic macular retinoschisis. Features seen on enhanced SD-OCT images were identified and compared between eyes with and without foveal detachment.


Results


On enhanced SD-OCT images, the retinoschisis in the outer retina was accompanied by splitting in the inner plexiform layer (IPL) in 11 eyes (50.0%) and a detachment of the inner limiting membrane (ILM) in 11 eyes (50.0%) in the superior and/or inferior peripheral macula; 9 eyes (42.9%) had both features. Multiple columnar structures were seen throughout the outer retinoschisis in 20 of 21 eyes (95.2%), and in ILM detachment/IPL retinoschisis in all eyes. Thirteen eyes had or progressed to a foveal detachment; an ILM detachment developed in 10 eyes (76.9%) with a foveal detachment and in 1 eye (12.5%) without a foveal detachment ( P = .008). IPL retinoschisis was detected in 8 eyes (61.5%) with a foveal detachment and 3 eyes (37.5%) without a foveal detachment, but this difference was not significant.


Conclusions


An ILM detachment in the superior and/or inferior peripheral macula was associated with a foveal retinal detachment in highly myopic eyes with macular retinoschisis. This feature may indicate strong tractional forces on the ILM that are transmitted to the outer retina through the dense columnar structures, resulting in a foveal retinal detachment.


Optical coherence tomography (OCT) has shown that myopic macular retinoschisis (also called foveoschisis) is not uncommon in highly myopic eyes. Retinoschisis was detected in 9% to 34% of highly myopic eyes with a posterior staphyloma. Based on the OCT features of untreated and treated eyes, the pathogenesis of myopic macular retinoschisis has been attributed to strong traction on the retina exerted by residual posterior vitreous cortex, an internal limiting membrane (ILM), retinal vessels, or a combination of these. Axial length elongation and/or formation of posterior staphyloma in highly myopic eyes may generate the inward tractional force exerted by these factors. This is strongly supported by the remission of the retinoschisis after vitrectomy combined with ILM peeling, which theoretically releases the tractional forces exerted by the posterior vitreous cortex and the ILM and partly by the retinal vessels in the area from which the ILM was peeled.


Myopic macular retinoschisis progresses to a retinal detachment in 21% to 43% of eyes, whereas this disease is often stable for many years without progression to a retinal detachment in other eyes. Development of a foveal retinal detachment in myopic macular retinoschisis impairs vision more severely. Thus, it is clinically important to identify the risk of progression of macular retinoschisis to a foveal retinal detachment. However, it is difficult to determine which eyes with myopic macular retinoschisis develop a retinal detachment. With more recently developed spectral-domain (SD) OCT technology, macular features can be visualized in great detail. Commercially available SD-OCT instruments acquire images 43 to 133 times faster than time-domain (Stratus) OCT instruments. High-speed imaging allows acquisition of high-definition SD-OCT B-scan images or averaging of multiple OCT B-scans at each location of interest on the retina to reduce speckle noise, thus providing a more detailed view of the macular anatomy. In the current study, we evaluated SD-OCT images enhanced by high definition or reduction of speckle noise obtained from eyes with myopic foveoschisis to differentiate the morphologic characteristics between eyes with and without a retinal detachment.


Methods


Twenty-one highly myopic eyes of 19 patients (3 men, 16 women) with macular retinoschisis who underwent enhanced SD-OCT examinations were included. In this study, eyes with an axial length equal to or greater than 26.00 mm were defined as highly myopic.


All patients underwent comprehensive ophthalmologic examinations, including autorefractometry, uncorrected and best-corrected visual acuity measurements using the 5-meter Landolt chart, axial length measurement using the IOL Master (Carl Zeiss Meditec, Dublin, California, USA), slit-lamp examinations, intraocular pressure measurements using Goldmann applanation tonometry, dilated indirect slit-lamp biomicroscopy, and color fundus photography.


Enhanced SD-OCT Examination


Experienced ophthalmologists examined all eyes using primarily SD-OCT instruments. Enhanced SD-OCT imaging was performed with the Spectralis HRA+OCT system (Heidelberg Engineering, Heidelberg, Germany), RTVue-100 (Optovue, Fremont, California, USA), and/or Cirrus HD-OCT (Carl Zeiss Meditec) to investigate the retinal microstructures. Enhancement of the B-scan images was achieved by reducing the speckle noise in Spectralis HRA+OCT and RTVue-100 by averaging 12 to 50 multiple OCT B-scans at each precise location of interest on the retina. Enhancement of the B-scans in Cirrus HD-OCT was achieved by acquisition of high-definition 6-mm B-scans (4096 axial scans/image) in 0.3 second per image.




Results


The demographic data from all the patients (16 women, 3 men) are shown in Table 1 . The ages of the patients ranged from 37 to 77 years (mean ± SD, 65.9 ± 6.6 years). The axial lengths ranged from 26.8 to 34.2 mm (mean ± SD, 29.7 ± 2.0 mm). Of the 21 eyes, 20 (95.2%) had posterior staphyloma.



TABLE 1

Demographics and Tomographic Features of Patients with Myopic Macular Retinoschisis






















































































































































































































































Case Age (Years)/ Gender R/L Axial Length (mm) Posterior Staphyloma Foveal RD Columnar Structure ILM Detachment Schisis in IPL PHM
1 74/F R 27.05 + + + + +
2 71/F R 28.20 + + +
3 54/F R 28.42 + + + +
4 72/F R 29.33 + + + + +
5 60/F R 29.37 + + +
6 54/F L 29.45 + + + + +
7 66/F L 30.11 + + + + +
8 64/M R 30.70 + +
9 63/M L 33.45 + + + + +
10 64/M L 28.22 + + + +
11 65/F L 28.45 + + + + +
12 37/F L 26.83 + + + + +
13 78/F R 28.72 + + + + +
14 70/F R 30.66 + + +
15 77/F L 33.00 + +
16 70/F R 30.61 + +
L 27.73 + +
17 74/F R 28.78 + + + +
18 60/F R 34.17 + + +
19 68/F R 29.64 + + +
L 30.10 + + +

+ = present; − = absent; F = female; ILM = inner limiting membrane; IPL = inner plexiform layer; L = left; M = male; PHM = posterior hyaloid membrane; R = right; RD = retinal detachment.


On OCT images, myopic macular retinoschisis in the outer retina was seen in all eyes. On enhanced SD-OCT images, splitting of the outer retina appeared to be present between the outer plexiform layer and the outer nuclear layer, because in all eyes the highly reflective layer representing the inner plexiform layer and 2 highly reflective lines representing the external limiting membrane (ELM) and the photoreceptor inner and outer segment junction (IS/OS) were seen in the anterior and posterior borders of the retinoschisis, respectively ( Figures 1, 2, 3 , and 4 ). In 20 of 21 eyes (95.2%), multiple columnar structures were seen widely within the retinoschisis as long, straight, highly reflective lines at the fovea and throughout the retinoschisis. In 6 eyes (28.6%) in which progression to a foveal retinal detachment was observed during follow-up, the columnar structures within the area of the retinal detachment shortened markedly and lost the columnar shape as if they shrank ( Figure 3 ). In addition to the retinoschisis in the outer retina, there were 2 other intraretinal separations on the SD-OCT images. Retinoschisis was found at the level of the inner plexiform layer (IPL; termed IPL schisis in this study) in 11 eyes (50.0%), an inner limiting membrane (ILM) detachment was seen in 11 eyes (52.4%), and both the features were found in 9 eyes (42.9%). In the space beneath the ILM and within the IPL retinoschisis, multiple columnar structures were observed similar to those seen in the retinoschisis in the outer retina ( Figures 1 and 2 ). The ILM detachment was in the superior and/or inferior peripheral macula on vertical B-scans in all 11 eyes, but it was seen in only 2 eyes on the horizontal B-scans. A comparison with simultaneously obtained infrared images indicated that the retinal vessels were present in the area of the ILM detachments in all eyes ( Figures 1 and 2 ). Microfolds were seen in 2 of the 21 eyes (9.5%), which corresponded to a retinal vessel; 1 was seen within an area with an ILM detachment and IPL retinoschisis ( Figure 2 ) and the other was not associated with these features ( Figure 3 ). A posterior hyaloid membrane was seen in only 3 eyes (14.3%) ( Figure 4 ).




FIGURE 1


Representative images show an internal limiting membrane (ILM) detachment in the inferior peripheral macula in an eye with a foveal retinal detachment (Patient 1). The best-corrected visual acuity is 0.2. (Top left, and Middle left) Infrared fundus photographs show the green scan lines of the enhanced spectral-domain optical coherence tomography (SD-OCT, Spectralis HRA+OCT) images in Top, and Middle right, respectively. The red and blue arrows indicate the points at which the scan line crosses the retinal vessels, which correspond to the red and blue arrowheads, respectively, in Top right. (Top, and Middle right) Vertical and horizontal 9-mm enhanced SD-OCT B-scans show macular retinoschisis and a foveal retinal detachment. (Top right) The ILM detachment (white arrows) and inner nuclear layer schisis are seen between the red arrowheads in the inferior peripheral macula along the vertical scan. The superior point (blue arrow) corresponding to a retinal arteriole does not show any features such as a retinal microfold or ILM detachment. Multiple columnar structures are seen in the hyporeflective spaces within the ILM detachment and outer retinoschisis. (Bottom) The magnified (2×) view of the area outlined by red dashed lines in the SD-OCT images in Middle right. A hyporeflective space with multiple columnar structures is present between the highly reflective outer plexiform layer (OPL) and highly reflective lines representing the external limiting membrane (ELM) and the photoreceptor inner and outer segment layer junction (IS/OS).



FIGURE 2


Representative images show an internal limiting membrane (ILM) detachment in the inferior and superior peripheral macula in an eye with foveal retinal detachment (Patient 11). The best-corrected visual acuity is 0.1. (Top left) Color fundus photograph. (Middle left) An infrared fundus photograph shows the red scan lines (*, †, and §). (Top, Middle, and Bottom center) Vertical (* and †) and horizontal (§) 6-mm enhanced spectral-domain optical coherence tomography (SD-OCT, Cirrus HD-OCT) images. (Top, Middle, and Bottom right) The magnified (2×) views of the areas outlined by red dashed lines in the SD-OCT images in Top, Middle, and Bottom center, respectively. The red and blue arrows (Middle left) indicate the points at which the scan line crosses the retinal vessels, which are indicated by the red and blue arrowheads (Top, and Middle center, and Middle right), respectively, in the vertical SD-OCT images. The vertical enhanced SD-OCT B-scans show macular retinoschisis and a foveal retinal detachment. The ILM detachment (white arrows) and inner plexiform layer (IPL) schisis are seen in areas including the retinal microfold at the point at which the scan crosses the retinal vessels, as shown by the red arrowhead in the inferior peripheral macula along a vertical scan. The crossing point indicated by the blue arrowhead does not show a retinal microfold. IPL schisis is also seen in the superior macula peripheral to the crossing point. Multiple columnar structures are evident in the hyporeflective spaces within the ILM detachment, IPL retinoschisis, and outer retinoschisis. A hyporeflective space with multiple columnar structures is present between the highly reflective outer plexiform layer (OPL) and highly reflective lines representing the external limiting membrane (ELM) and the photoreceptor inner and outer segment layer junction (IS/OS).



FIGURE 3


Images of an eye that progressed to a foveal retinal detachment without an internal limiting membrane (ILM) detachment (Patient 2). This is an exceptional case in which a foveal retinal detachment developed, but no ILM detachment was found at any time during the progression. The images from this case are shown because the entire process of foveal retinal detachment formation is well documented. (Top left) A color fundus photograph shows the scan lines (white lines) in Second, Third, Fourth, and Fifth row left. (Top center) An infrared fundus photograph shows multiple punctuate lesions corresponding to the columnar structures in the outer retinoschisis. (Top right) An infrared fundus photograph shows the green scan lines in Sixth row, and Bottom. (Second, Fourth, Fifth, and Sixth row left) Horizontal enhanced spectral-domain optical coherence tomography images. (Third row, and Bottom left) Vertical enhanced SD-OCT. (Second to Fifth row left) Six-mm-length B-scans in RTVue-100; (Sixth row, and Bottom left) 9-mm-length B-scans in Spectralis HRA+OCT. (Second, Third, Fourth, Fifth, and Sixth row right) Magnified (2×) views of the areas outlined by red dashed lines on SD-OCT images in Second, Third, Fourth, Fifth, and Sixth row left, respectively. The OCT images were obtained at the initial visit (Second row, and Third row), and 1 month (Fourth row), 2 months (Fifth row), and 5 months (Sixth row, and Bottom) after the initial visit. At the initial visit, the foveal photoreceptor layer appears intact based on the visibility of the highly reflective lines representing the external limiting membrane (ELM) and the photoreceptor inner and outer segment layer junction (IS/OS). At 1 month, a small area in the temporal juxtafovea shows a retinal detachment. At 2 months, the retinal detachment includes the whole fovea. At 5 months, the foveal detachment has enlarged, and consequent disruption of the outer photoreceptor layer is seen. The best-corrected visual acuity was 0.6, 0.6, 0.3, and 0.3 at the initial visit and at 1 month, 2 months, and 5 months after the initial visit, respectively. During progression to a foveal retinal detachment, the columnar structures indicated by white arrows gradually shrank and did not resemble a column. (Top left, and Top right) The red arrows point to where the scan lines cross the retinal vessels, indicated by red arrowheads in the vertical SD-OCT images (Third row, and Bottom). No ILM detachment or microfolds are seen.



FIGURE 4


Images from an eye that did not progress to a foveal retinal detachment for many years without internal limiting membrane detachment (Patient 14). (Top left) A color fundus photograph shows the scan lines (white lines) of optical coherence tomography (OCT) images in Top, Second, Third, and Fourth row right. (Top, Second, and Third row right) Time-domain (TD) OCT (Stratus OCT) B-scan images at the same horizontal scan. (Top right) The initial visit; (Second row right) 6 months after the initial visit; (Third right) 26 months after the initial visit. The white arrows indicate the central edge of the posterior hyaloid membrane detachment. The red arrows indicate the peripheral ends of the retinoschisis in the outer retina. As the posterior hyaloid membrane detachment progressed, the area of the retinoschisis narrowed, and the height of the foveoschisis appeared to increase, but no foveal detachment developed. (Second row left, and Fourth row right) Spectral-domain OCT (SD-OCT, Cirrus OCT) B-scans at the same location and time as the TD-OCT image in Third row right. (Second row left) A magnified (2×) view of the area outlined by red dashed lines in the SD-OCT images in Fourth row right. The highly reflective lines representing the external limiting membrane (ELM) and the photoreceptor inner and outer segment layer junction (IS/OS) is nearly intact. (Bottom left) An infrared image simultaneously obtained with SD-OCT images in (Fifth row, and Bottom right) horizontal (Fifth row right) and vertical (Bottom right) 9-mm length SD-OCT B-scan images (Spectralis HRA+OCT) obtained 33 months after the initial visit. The best-corrected visual acuity was stable during the 33 months (0.7, 0.7, 0.6, and 0.7 at the initial visit and at 6, 26, and 33 months after the initial visit, respectively). (Bottom left) The red and blue arrows indicate the points where the scan lines cross the vessels, indicated by (Bottom right) the red and blue arrowheads, respectively. There is a microfold (red arrowhead) at a point corresponding to the retinal vessel but no ILM detachment.

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Jan 17, 2017 | Posted by in OPHTHALMOLOGY | Comments Off on Features Associated With Foveal Retinal Detachment in Myopic Macular Retinoschisis

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