Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contacts Login 
  • Users Online: 2743
  • Home
  • Print this page
  • Email this page

   Table of Contents      
PHOTO ESSAY
Year : 2020  |  Volume : 68  |  Issue : 3  |  Page : 516-517

Aborted bridge coloboma with scleral fistula


1 Department of Vitreoretina Services, Disha Eye Hospitals, Kolkata, West Bengal, India
2 Department of Ocular Pathology, Uveitis and Neuro-Ophthalmology Services, Sri Sankaradeva Nethralaya, Guwahati, Assam, India

Date of Submission16-Aug-2019
Date of Acceptance12-Sep-2019
Date of Web Publication14-Feb-2020

Correspondence Address:
Dr. Debdulal Chakraborty
Department of Vitreoretina Services, Disha Eye Hospitals, Ghosh Para Road, Barrackpore, Kolkata - - 700 120, West Bengal
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijo.IJO_1503_19

Rights and Permissions

Keywords: Coloboma, scleral fistula, Optos


How to cite this article:
Chakraborty D, Das D. Aborted bridge coloboma with scleral fistula. Indian J Ophthalmol 2020;68:516-7

How to cite this URL:
Chakraborty D, Das D. Aborted bridge coloboma with scleral fistula. Indian J Ophthalmol [serial online] 2020 [cited 2020 Jun 3];68:516-7. Available from: http://www.ijo.in/text.asp?2020/68/3/516/278352



A 66-year-old with best-corrected visual acuity 20/20 in both eyes was detected with retinochoroidal coloboma (RCC) [Figure 1], 1 disc diameter (DD) inferior to disc. The coloboma could be clearly divided into two parts, the superior part showing a scleral fistula. In the central part of the coloboma, there was a bridge of retinal tissue extending from the nasal edge of the coloboma for approximately 3.5DD. The temporal part of the bridge was devoid of any retinal tissue [Figure 1] and [Figure 2]. The remaining fundus was unremarkable. Intraocular pressure (IOP) was 8 mmHg. The axial length was 22.83 mm. “En-face” optical coherence tomography (OCT) [Figure 3] and- B-scan [Figure 4] and Supplementary Video 1] revealed a discontinuity of the sclera in the region of the fistula. The OCT scan [Figure 2] passing through the area of the aborted bridge of retinal tissue showed poorly differentiated retinal tissue in the nasal half and the intercalary membrane with schisis in the center of the bridge, extending toward the temporal periphery of the coloboma. The transitional zone in the temporal periphery showed subclinical retinal detachment. Partially preserved choroid with large choroidal vessels could also be seen in the region of the aborted bridge.
Figure 1: Optos image showing retinochoroidal coloboma with scleral fistula (red arrowhead) and aborted bridge (white arrowhead)

Click here to view
Figure 2: Structural OCT image of the aborted bridge area showing poorly differentiated retinal tissue (white star), the intercalary membrane with schisis (pink star), area of subclinical retinal detachment (pink polygon), sclera (pink arrowhead), and choroidal tissue (yellow arrowhead)

Click here to view
Figure 3: En face OCT and structural OCT showing fistula opening (white star)

Click here to view
Figure 4: Ultrasound B-scan showing the coloboma with fistula (white arrowhead)

Click here to view






  Discussion Top


Ultra-wide-field image of RCC with scleral fistula has never been reported. We could find only two reports[1],[2] of scleral fistula in RCC, both needing treatment for the closure of the fistula. The low IOP noted in this patient did not cause hypotony maculopathy noted by Gupta et al.[1] and inflammation noted by Mori et al.[2] En face OCT showed the fistulous opening that had never been described. In the region of the aborted bridge of retinal tissue, the choroidal layer could be detected on structural OCT. The temporal periphery of the RCC showed a subclinical retinal detachment, which has been described by Gopal et al.[3] B scan ultrasonography showed a well-defined area of retinochoroidal excavation inferior to the disc, with an area of absence of all three coats of the eye, suggestive of scleral fistula.


  Conclusion Top


The use of Optos, OCT, and B-scan together can help us understand and evaluate these patients in a better way.

Acknowledgements

We would like to thank: Mr Sudip Ghosh, Ophthalmic photographer. Disha Eye Hospitals Kolkata, West Bengal, India.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Gupta A, Narang S, Gupta V, Sharma A, Pandav SS, Singh P. Successful closure of spontaneous scleral fistula in retinochoroidal coloboma. Arch Ophthalmol:2001;119:1220-1  Back to cited text no. 1
    
2.
Mori S, Komatsu H, Watari H. Spontaneouspos- terior bulbar perforation of congenital scleral colo- boma and its surgical treatment: A case report. Ophthalmic Surg 1985;16:433-6.  Back to cited text no. 2
    
3.
Gopal L, Khan B, Jain S, Prakash VS. A clinical and optical coherence tomography study of the margins of choroidal colobomas. Ophthalmology 2007;114:571-80.  Back to cited text no. 3
    


    Figures

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



 

Top
 
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
Discussion
Conclusion
References
Article Figures

 Article Access Statistics
    Viewed181    
    Printed0    
    Emailed0    
    PDF Downloaded72    
    Comments [Add]    

Recommend this journal