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   Table of Contents      
BRIEF COMMUNICATION
Year : 2014  |  Volume : 62  |  Issue : 4  |  Page : 513-515

Bilateral foveal retinoschisis accompanying unilateral peripheral retinoschisis


1 Department of Ophthalmology, Dokuz Eylul University School of Medicine, Izmir, Turkey
2 Dr. Behçet Uz Children's Hospital, Izmir, Turkey

Date of Submission06-Apr-2011
Date of Acceptance06-Dec-2014
Date of Web Publication8-May-2014

Correspondence Address:
Nilufer Kocak
Department of Ophthalmology, Dokuz Eylul University School of Medicine, Inciralti, Balçova 35340, Izmir
Turkey
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0301-4738.100005

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  Abstract 

X-linked juvenile retinoschisis is a rare hereditary retinal disease characterized by a tangential splitting of the neurosensory retina which may cause early-onset visual impairment. Existence of the retinal neurosensory layer splitting on cross-sectional images of optical coherance tomography (OCT) and the absence of leakage on fluorescein angiography (FA) help confirming the diagnosis. Such diagnostic tests are also helpful in determining the management of the disease. However, most of the retinoschisis cavities remain stable and rarely extend to the posterior pole, many authors suggest laser prophylaxis to avoid the potential risk of retinal detachment due to holes in the outer retinal layer. Herein, we report a case with bilateral foveal retinoschisis accompanying unilateral peripheral retinoschisis who was evaluated with detailed ophthalmologic examination. Visual acuity, fundoscopy, OCT, and FA remained stable in the second year of follow-up after prophylactic argon laser treatment.

Keywords: Fluorescein angiography, optical coherance tomography, prophylactic argon laser treatment, retinoschisis


How to cite this article:
Kocak N, Ozturk TA, Kaynak S. Bilateral foveal retinoschisis accompanying unilateral peripheral retinoschisis. Indian J Ophthalmol 2014;62:513-5

How to cite this URL:
Kocak N, Ozturk TA, Kaynak S. Bilateral foveal retinoschisis accompanying unilateral peripheral retinoschisis. Indian J Ophthalmol [serial online] 2014 [cited 2019 Dec 6];62:513-5. Available from: http://www.ijo.in/text.asp?2014/62/4/513/100005

Visual deterioration that progresses during the first to second decades of life is the most common symptom of retinoschisis, while amblyopia, strabismus, and nystagmus related with retinal detachment and vitreous hemorrhage may also be seen. [1],[2] The main clinical feature is foveal schisis with cystoid spaces and fine radial striae located in the macula. Peripheral retinoschisis occurs in approximately 50% of affected male patients. Vitreous hemorrhage, retinal detachment, and neovascular glaucoma may also be seen. [3],[4] Although there is no proven theuropeutic approach for this disease, laser photocoagulation, cryotherapy, scleral buckle, and pars plana vitrectomy are considered as the main treatment options for retinoschisis especially complicated with vitreous hemorrhage or retinal detachment. [4],[5],[6],[7],[8]


  Case Report Top


A 11-year-old boy was referred with complaints of bilateral blurred vision. The best corrected visual acuities were 10/20 in the right eye and 20/200 in the fellow eye. Anterior segment examination with slit lamp biomicroscopy was unremarkable. Fundoscopic examination via indirect ophthalmoscopy revealed minimal macular edema in the right eye and diffuse pigmentary changes as well as peripheral retinoschisis in the fellow eye [Figure 1]. Cartwheel-like configurated radial striates as well as fine cystoid changes in macula were seen in fluorescein angiography (FA) of the right eye and diffuse punctate filling defects were revealed in FA of the left eye [Figure 2]. Bilateral foveal retinoschisis was evident on optical coherance tomography (OCT) [Figure 3]. Bilateral subnormal rod responses in scotopic electroretinogram (ERG) and subnormal flicker responses were present; however, they were more pronounced in the left eye. Bilateral negative maximum responses in scotopic ERG were also detected. Besides, a selective decrease in b-wave amplitude on photopic cone responses which is characteristic for retinoschisis was evident for the subject.
Figure 1: Clinical photographs of right (a) and left (b) fundus. Peripheral retinoschisis in the left eye (c); laser spots around the peripheral retinoschisis lesion (d)

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Figure 2: Radial striates and fine cystoid changes of the right eye (a) and diffuse punctate filling defects of the fellow eye (b) in fluorescein angiography

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Figure 3: Foveal retinoschisis in the OCT images of right (a) and left (b) fundus; OCT images of right (c) and left (d) fundus at the second year of follow-up

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In order to avoid the potential risk of retinal detachment, argon laser photocoagulation was performed around the peripheral retinoschisis lesion in the left eye [Figure 1]. After the second year of follow-up visual acuity remained stable, also FA [Figure 3] and OCT [Figure 4] revealed no progression in time.
Figure 4: Fluorescein angiography of right (a) and left (b) fundus at the second year of follow-up. Peripheral retinoschisis lesion at the second year of follow-up (c)

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  Discussion Top


The constant diagnostic feature of XLRS is bilateral foveal retinoschisis, whereas peripheral retinoschisis may be present approximately half of the affected male patients. Tangential splitting of the neurosensory retina caused by the defect of cellular adhesion and cell-cell interactions within the inner nuclear layer is main histopatological appereance. However, disease is commonly presented with reading difficulties due to the foveoschisis in school-age children, it can be diagnosed with nystagmus or strabismus in infancy. Prognosis is poor because of the progressive maculopathy, moreover sudden visual loss due to retinal detachment or intravitreal hemorrhage may be seen in cases with peripheral retinoschisis. [1],[2],[3]

Clinical photographs of retina and cross-sectional images of OCT help confirming the diagnosis and determining the management of the disease. Existence of mild window defects and absence of fluorescein leakage on FA as well as presence of a selective decrease in b-wave amplitude on both scotopic and photopic testing of ERG are also characteristic findings for differential diagnosis. [1],[2],[5],[9] Confirming RS1 gene mutations on genetic molecular testing is an emerging diagnostic parameter for the affected patients without a family history. [3],[10]

However most of the retinoschisis cavities remain stable and rarely extend to the posterior pole, many authors suggest laser prophylaxis. Malagola et al. [7] reported the success of prophylactic argon laser photocoagulation in the asymptomatic stage of bullous retinoschisis with outer layer breaks. Gopal et al. [4] also reported the beneficial effect of prophylactic photocoagulation in collapsing the schisis cavities. Successful treatment with laser photocoagulation in one of three cases of posteriorly situated retinoschisis-retinal detachment was reported by Ambler et al. [8] Jo et al. [5] published the data of the first case of spontaneous regression of retinoschisis as observed by OCT in the literature. On the other hand, some authors do not recommend prophylactic treatment of retinoschisis in the absence of combined retinal detachment; moreover, they stated the increased risk of retinal tears and iatrogenic retinal detachments after the heavy photocoagulation burns. [4],[6],[9] In the present case, we performed prophylactic argon laser photocoagulation to the posterior margin of retinoschisis cavity. At the end of the second year of follow-up, both fundoscopic examination and visual assessment remained stable. Although there is no proven guideline for both the laser prophylaxis and the treatment of retinoschisis, laser photocoagulation, cryotherapy, scleral buckle, and parsplana vitrectomy are considered as the main treatment options especially in cases with vitreous hemorrhage or retinal detachment.


  Acknowledgments Top


The present study was conducted at the Ophthalmology Department in Dokuz Eylul University School of Medicine, Izmir, Turkey.

 
  References Top

1.
Yu J, Ni Y, Keane PA, Jiang C, Wang W, Xu G. Foveomacular schisis in juvenile X-linked retinoschisis: An optical coherence tomography study. Am J Ophthalmol 2010;149:973-8.  Back to cited text no. 1
    
2.
George ND, Yates JR, Moore AT. X linked retinoschisis. Br J Ophthalmol 1995;79:697-702.  Back to cited text no. 2
    
3.
Xu J, Gu M, Ma K, Liu X, Snellingen T, Sun E, et al. R213W mutation in the retinoschisis 1 gene causes X-linked juvenile retinoschisis in a large Chinese family. Mol Vis 2010;16:1593-600.  Back to cited text no. 3
    
4.
Gopal L, Shanmugam MP, Battu RR, Shetty NS. Congenital retinoschisis: Successful collapse with photocoagulation. Indian J Ophthalmol 2001;49:265-6.  Back to cited text no. 4
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5.
Jo YJ, Kim KN, Kim JY. Spontaneous resolution of foveal cysts associated with X-linked retinoschisis as observed by optical coherence tomography. Can J Ophthalmol 2010;45:1-2.  Back to cited text no. 5
    
6.
Johnson DL, Nieto JC, Ip MS. Retinal detachment due to an outer retinal tear following laser prophylaxis for retinoschisis. Arch Ophthalmol 2008;126:1775-6.  Back to cited text no. 6
    
7.
Malagola R, Contestabile MT, Villani GM, De Santis EM, Recupero SM. Outer layer breaks and asymptomatic schisis detachment: Clinical considerations. Ophthalmic Surg Lasers 2002;33:268-72.  Back to cited text no. 7
    
8.
Ambler JS, Gass JD, Gutman FA. Symptomatic retinoschisis-detachment involving the macula. Am J Ophthalmol 1991;112:8-14.  Back to cited text no. 8
    
9.
Sikkink SK, Biswas SB, Parry NR, Stanga PE, Trump D. X-linked retinoschisis: An update. J Med Genet 2007;44:225-32.  Back to cited text no. 9
    
10.
Kim JE, Ruttum MS, Koeberl MJ, Hassemer EL, Sidjanin DJ. Genetics and clinical evaluation of juvenile retinoschisis. J AAPOS 2009;13:215-7.  Back to cited text no. 10
    


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4]



 

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