Glyxambi
Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contacts Login 
  • Users Online: 126
  • Home
  • Print this page
  • Email this page


 
   Table of Contents      
PHOTO ESSAY
Year : 2018  |  Volume : 66  |  Issue : 4  |  Page : 570-571

Bilateral multifocal retinal pigment epithelium detachment and pachychoroidopathy


Department of Retina and Vitreous, Aravind Eye Care System, Puducherry, India

Date of Submission01-Nov-2017
Date of Acceptance29-Dec-2017
Date of Web Publication26-Mar-2018

Correspondence Address:
Dr. Chokkahalli K Nagesha
Aravind Eye Care System, Puducherry
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijo.IJO_1070_17

Rights and Permissions
  Abstract 


Keywords: Central serous chorioretinopathy, pachychoroid, pigmented epithelial detachment


How to cite this article:
Nagesha CK, Megbelayin EO. Bilateral multifocal retinal pigment epithelium detachment and pachychoroidopathy. Indian J Ophthalmol 2018;66:570-1

How to cite this URL:
Nagesha CK, Megbelayin EO. Bilateral multifocal retinal pigment epithelium detachment and pachychoroidopathy. Indian J Ophthalmol [serial online] 2018 [cited 2018 Sep 22];66:570-1. Available from: http://www.ijo.in/text.asp?2018/66/4/570/228463



Idiopathic bilateral multifocal retinal pigment epithelial detachment (RPED) is an extremely rare condition and is often observed as an incidental clinical finding. The exact pathophysiology and natural course of this disease is not known. We observed a case of multifocal RPED in otherwise asymptomatic middle-aged female. Multimodal imaging confirmed the diagnosis of RPED associated with pachychoroid features, which were not described before, and foci of central serous chorioretinopathy. The benign nature of this entity and role of multimodal imaging has been emphasized in this case.


  Case Report Top


A 52-year-old woman after presbyopic correction, presented to retina clinic for routine fundus evaluation. The best-corrected visual acuity of both eyes was 20/20 and had no major systemic illness. Fundus examination of both eyes showed multiple retinal pigment epithelial detachments (RPEDs) distributed throughout the fundus and concentrated more in the posterior pole [Figure 1]a and [Figure 1]b which shows hyperautofluorescence on blue reflectance [Figure 1]c and [Figure 1]d. Spectral-domain optical coherence tomography (SD-OCT) revealed serous nature of the PEDs with underlying pachychoroid features [Figure 2]e and [Figure 2]j. A small pocket of subretinal fluid was noted along superior arcade of the right eye, which showed central serous chorioretinopathy (CSR)-like leak on fundus fluorescein angiography (FFA) [Figure 3]. All the PEDs were initially hypofluorescent followed by hyperfluorescent on FFA and varied cyanescence on indocyanine green angiography (ICGA) [Figure 2]a,[Figure 2]b,[Figure 2]c,[Figure 2]d, [Figure 2]f,[Figure 2]g,[Figure 2]h,[Figure 2]i with no evidence of choroidal neovascular membrane (CNVM) or polypoidal choroidal vasculopathy (PCV).
Figure 1: Color fundus photo of right (a) and left (b) eye showing well-circumscribed multiple retinal pigment epithelial detachments throughout the macula, which are hyperautofluorescent (c and d)

Click here to view
Figure 2: Fundus fluorescein angiography of both eyes shows progressive filling of dye in all pigment epithelial detachments (a and d, right eye; e and g, left eye) whereas indocyanine green angiography shows initial hypocyanescence of pigment epithelial detachments and in late phases it shows mixed hypo- and hypercyanescence (c and d, right eye; h and i, left eye). Optical coherence tomography passing through macula shows pigment epithelial detachment with internal hyporeflectivity suggestive of serous nature and the presence of pachyvessels (cross star) (arrow head and arrow show pigment epithelial detachment with hypo- and hypercyanescence at late phase indocyanine green angiography in image d). Subfoveal choroidal thickness OD: 338 μ, OS: 364 μ and pachyvessel diameter: 229 μ

Click here to view
Figure 3: Fundus fluorescein angiography shows central serous chorioretinopathy-like leak along superior arcade (a, early phase; b, late phase) and corresponding indocyanine green angiography shows underlying pachyvessel (c) with leakage at late phase (d) optical coherence tomography passing through that region shows the presence of subretinal fluid (cross star) and underlying pachyvessel (arrowheads)

Click here to view



  Discussion Top


Idiopathic RPED is a rare condition for which pathogenesis and natural course is poorly understood. Widespread primary defect in adhesion between RPE and Bruch's membrane was assumed to be the cause for multiple RPEDs. Gass et al.[1] described the presence of inflammatory infiltrates in the choroidal layer and that of large choroidal vessels in histopathological section. Though majority are asymptomatic, they can develop complications such as hemorrhagic PED,[2] CNVM,[1] and CSR as in our case. The diagnosis is simple and OCT confirms serous nature of PEDs, but other differentials that should be borne in mind but not difficult to diagnose include photoreceptor-RPE diastasis, which predominantly presents as multifocal CSR [3] and nonbest multifocal vitelliform maculopathy in which yellow lesions are located in subretinal space and Doyne's honeycomb dystrophy which is distinguished by temporal distribution of drusen and family history.[4] Evaluation of this condition should include SD-OCT, FFA, and ICGA to rule out the presence of associated treatable conditions such as CNVM, PCV, and CSR.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.


  Conclusion Top


Multifocal RPED can be associated with pachychoroid features and foci of central serous chorioretinopathy. Multimodal imaging helps confirm the diagnosis and rule out simulating conditions.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Gass JD, Bressler SB, Akduman L, Olk J, Caskey PJ, Zimmerman LE, et al. Bilateral idiopathic multifocal retinal pigment epithelium detachments in otherwise healthy middle-aged adults: A clinicopathologic study. Retina 2005;25:304-10.  Back to cited text no. 1
    
2.
Klein ML, Obertynski H, Patz A, Fine SL, Kini M. Follow-up study of detachment of the retinal pigment epithelium. Br J Ophthalmol 1980;64:412-6.  Back to cited text no. 2
[PUBMED]    
3.
Li XQ, Pryds A, Carlsen J, Larsen M. Multifocal central serous chorioretinopathy with photoreceptor-retinal pigment epithelium diastasis in heritable pulmonary arterial hypertension. Retin Cases Brief Rep 2015;9:83-7.  Back to cited text no. 3
[PUBMED]    
4.
Gass JD. Stereoscopic Atlas of Macular Diseases: Diagnosis and Treatment. 4th ed. St. Louis: C.V. Mosby; 2012. p. 292-5.  Back to cited text no. 4
    


    Figures

  [Figure 1], [Figure 2], [Figure 3]



 

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
Abstract
Case Report
Discussion
Conclusion
References
Article Figures

 Article Access Statistics
    Viewed313    
    Printed0    
    Emailed0    
    PDF Downloaded117    
    Comments [Add]    

Recommend this journal