Literature DB >> 24104712

Bilateral central serous chorioretinopathy with retinal pigment epithelium tears following epidural steroid injection.

Sung-Bok Lee1, Jung-Yeul Kim, Woo-Jin Kim, Chul-Bum Cho, Takeshi Iwase, Young-Joon Jo.   

Abstract

The cause of central serous chorioretinopathy (CSC) is mostly idiopathic. Other cause such as stressful event or use of corticosteroid has been associated with severe form of CSC. Atypical presentation of CSC has widespread degeneration of retinal pigment epithelium (RPE) or bullous retinal detachment. In this report, we describe a case of bilateral CSC with RPE tear after epidural steroid injection.

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Year:  2013        PMID: 24104712      PMCID: PMC3831769          DOI: 10.4103/0301-4738.119441

Source DB:  PubMed          Journal:  Indian J Ophthalmol        ISSN: 0301-4738            Impact factor:   1.848


A 79-year-old man visited our clinic with a complain of deterioration in the visual acuity of right eye. Best corrected OD visual acuity was 20/32, and OS was 20/25. Recently, he had had four epidural injections of triamcinolone and dexamethasone for chronic back pain. In fundus examination, dark-gray colored lesions were detected in both eyes that were associated with dome-shape large elevated lesion of retinal pigment epithelium (RPE). Inferior serous retinal detachment was observed in both eyes. On fluorescein angiography (FA), the pigment epithelial detachment (PED) lesion showed round, well-demarcated uniform hypofluorescence in the early phase and pooling in the late phase [Figs. 1 and 2]. In contrast, the late phase of ICGA demonstrated persistent hypofluorescence. RPE tear, which was dark-gray colored lesion, showed hyperfluorescence from the early phase of FA and was still hyperfluorescent with staining into the surrounding tissue in the late phase. On spectral domain-optical coherence tomography (SD-OCT), tear- and rolled-edge of RPE was observed [Fig. 3]. Corticosteroid treatment was discontinued without any treatment. One month later, although the area of serous retinal detachment was decreased, the RPE tear was enlarged inferiorly and the visual acuity in the right eye decreased to 20/100.
Figure 1

Fundus photograph of both eyes showing neurosensory retinal detachment in the macular region. The gray-colored lesions reveal retinal pigment epithelium tear. (a) Right eye, (b) Left eye, and (c) At 1 month after first visit. The lesion is progressing into larger regions

Figure 2

(a, e) Early-phase fluorescein angiography (FA) showing well-demarcated area of hypofluorescence corresponding to the pigment epithelial detachment (PED) and hyperfluorescence due to window defect of retinal pigment epithelium (RPE) tear. (b, f) Late-phase FA revealing hyperfluorescence of PED and strong hyperfluorescence area of RPE tear. (c, d, g, h) Early-phase indocyanine green angiography showing area of hypofluorescence of PED that persisted in the late-phase and hyperfluorescence of the RPE tear lesion, followed by decrease of fluorescence on the late-phase

Figure 3

Spectral domain optical coherence tomography shows serous pigment epithelial detachment with pigment epithelial tears and rolled edge (red arrows)

Fundus photograph of both eyes showing neurosensory retinal detachment in the macular region. The gray-colored lesions reveal retinal pigment epithelium tear. (a) Right eye, (b) Left eye, and (c) At 1 month after first visit. The lesion is progressing into larger regions (a, e) Early-phase fluorescein angiography (FA) showing well-demarcated area of hypofluorescence corresponding to the pigment epithelial detachment (PED) and hyperfluorescence due to window defect of retinal pigment epithelium (RPE) tear. (b, f) Late-phase FA revealing hyperfluorescence of PED and strong hyperfluorescence area of RPE tear. (c, d, g, h) Early-phase indocyanine green angiography showing area of hypofluorescence of PED that persisted in the late-phase and hyperfluorescence of the RPE tear lesion, followed by decrease of fluorescence on the late-phase Spectral domain optical coherence tomography shows serous pigment epithelial detachment with pigment epithelial tears and rolled edge (red arrows)

Discussion

Recent studies have considered steroids as a risk factor for acute central serous chorioretinopathy (CSC).[1] Steroids increase the development of CSC by impeding the healing of RPE injury and increasing the permeability of the choriocapillaris.[234] In most CSC patients, local serous retinal detachment occurs in the neurosensory retina or RPE and, if steroids are used, it is associated with atypical patterns, such as overall diffuse retinal pigment epitheliopathy.[5] We experienced the CSC with large PED and RPE tears after epidural steroid injection and could confirm the diagnosis by sp ecific findings of FA, ICGA, and OCT. These findings may help understand fundus and angiographic findings of the PED and RPE tears in various conditions.
  5 in total

Review 1.  Central serous chorioretinopathy and glucocorticoids.

Authors:  Evrydiki A Bouzas; Panagiotis Karadimas; Constantin J Pournaras
Journal:  Surv Ophthalmol       Date:  2002 Sep-Oct       Impact factor: 6.048

2.  Bilateral serous retinal detachment resembling central serous chorioretinopathy following epidural steroid injection.

Authors:  L Y Kao
Journal:  Retina       Date:  1998       Impact factor: 4.256

3.  Acute bilateral central serous chorioretinopathy following intra-articular injection of corticosteroid.

Authors:  Lakshmi Kanta Mondal; Krishnendu Sarkar; Himadri Datta; Pradip Ranjan Chatterjee
Journal:  Indian J Ophthalmol       Date:  2005-06       Impact factor: 1.848

4.  Central serous chorioretinopathy after epidural corticosteroid injection.

Authors:  T Iida; R F Spaide; S G Negrao; C A Carvalho; L A Yannuzzi
Journal:  Am J Ophthalmol       Date:  2001-09       Impact factor: 5.258

5.  Endogenous cortisol profile in patients with central serous chorioretinopathy.

Authors:  S P Garg; T Dada; D Talwar; N R Biswas
Journal:  Br J Ophthalmol       Date:  1997-11       Impact factor: 4.638

  5 in total
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1.  The giant tear of retinal pigment epithelium following focal laser in central serous chorioretinopathy.

Authors:  Avadhesh Oli; Divya Balakrishnan
Journal:  Rom J Ophthalmol       Date:  2020 Jul-Sep

2.  Retinal pigment epithelial tears in the era of intravitreal pharmacotherapy: risk factors, pathogenesis, prognosis and treatment (an American Ophthalmological Society thesis).

Authors:  David Sarraf; Anthony Joseph; Ehsan Rahimy
Journal:  Trans Am Ophthalmol Soc       Date:  2014-07

3.  Retinal pigment epithelium apertures as a late complication of longstanding serous pigment epithelium detachments in chronic central serous chorioretinopathy.

Authors:  Claudio Iovino; Jay Chhablani; Deepika C Parameswarappa; Marco Pellegrini; Giuseppe Giannaccare; Enrico Peiretti
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4.  Retinal Pigment Epithelium Tear after Immunosuppressive Treatment for Sarcoidosis-related Choroidal Granuloma.

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5.  Temporal Association between Topical Ophthalmic Corticosteroid and the Risk of Central Serous Chorioretinopathy.

Authors:  Yuh-Shin Chang; Shih-Feng Weng; Jhi-Joung Wang; Ren-Long Jan
Journal:  Int J Environ Res Public Health       Date:  2020-12-17       Impact factor: 3.390

6.  Bilateral retinal pigment epithelial tears in acute central serous chorioretinopathy without bullous retinal detachment: A case report.

Authors:  Woo Hyuk Lee; Bum Jun Kim; Yong Seop Han
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  6 in total

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