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DOI: 10.1055/a-2227-4037
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Effective Focal Laser Photocoagulation for Persistent Central Serous Chorioretinopathy: A Forgotten Technique

Effektive fokale Laser-Photokoagulation bei persistierender zentraler seröser Chorioretinopathie: eine vergessene Technik
Peter Kiraly
1   Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom of Great Britain and Northern Ireland
2   Nuffield Laboratory of Ophthalmology, University of Oxford Nuffield Laboratory of Ophthalmology, Oxford, United Kingdom of Great Britain and Northern Ireland
› Author Affiliations
 

Introduction

Central serous chorioretinopathy (CSC) ranks as the fourth most prevalent nonsurgical maculopathy. It is characterized by a thickened choroid, pigment epithelium (RPE) irregularities, and accumulation of subretinal fluid (SRF) [1], [2]. In acute CSC cases, visual impairment is typically confined to the area of SRF accumulation and improves once the SRF resolves [3]. In chronic CSC, where SRF fluids persists for at least 6 months, vision loss can become irreversible, potentially leading to severe visual impairment or even legal blindness [4]. Currently, there is no consensus on the duration of SRF persistence required to cause irreversible vision loss. The first treatment modality described for CSC was focal laser photocoagulation (FLP), targeting the site of focal leakage observed during fluorescein angiography (FA) [5], [6]. FLP involves utilizing a green or yellow laser beam to induce coagulation of tissue at and around the leaking area, effectively sealing the site of leakage [5]. Burumcek et al. demonstrated that CSC patients treated with focal FLP experienced faster resorption of SRF and improved visual acuity (VA) compared to those following a natural course [5]. A significant disadvantage of focal FLP is the possibility of treating only extrafoveal areas of leakage [7]. Moreover, scotoma and secondary choroidal neovascularization (CNV) have been described in CSC patients following treatment with FLP [8]. With the emergence of new treatment modalities, such as half-dose/fluence photodynamic therapy (PDT) [9], subthreshold micropulse laser (SML) treatment [9], and oral spironolactone/eplerenone treatment [10], FLP has largely fallen out of use. Large multicenter trials have compared half-dose PDT, SML, and mineralocorticoid receptor antagonists against each other [9], [11], demonstrating the superiority of PDT. Moreover, a study showed that eplerenone was not superior over a placebo in chronic CSC following a 12-month treatment period [12]. However, FLP has not been directly compared to alternative treatment modalities in big multicenter prospective trials. Although half-dose/fluence PDT is unequivocally the most effective treatment modality for chronic CSC, it is associated with high costs and limited availability due to a worldwide shortage of verteporfin [13], [14]. In the absence of any other effective treatment and with limited PDT availability, patients are often merely observed, experiencing fluctuating SRF and a steady, yet progressively irreversible, worsening of vision. In our case report, we present a patient with persistent CSC and extrafoveal pigment epithelial detachment (PED), who was on the waiting list to receive half-dose PDT treatment. Due to the extended waiting time, he opted for FLP treatment, which resulted in complete resolution of SRF and vision improvement within 1 month after the treatment.


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Case Report

A 33-year-old man presented with scotoma and metamorphopsia in the left eye, persisting for a few days. The patient has experienced 4 episodes of CSC, each resolving spontaneously within 2 – 3 months. He denied any use of exogenous steroids; however, he reported experiencing stress at work and at home due to a newborn baby. Best-corrected visual acuity (BCVA) in the right eye was 6/6, and 6/9 in the left eye; intraocular pressure was within normal limits. The slit lamp examination of the right eye was unremarkable. In the left eye, macular edema and pigmentary changes were observed. Optical coherence tomography (OCT) in the right eye revealed pachyvessels with normal choroidal thickness, with no RPE changes and/or SRF accumulation. OCT in the left eye revealed SRF accumulation under the fovea and superior to it, with small PED extrafoveally superiorly with subretinal hyperreflective material around the PED. Moreover, a thickened choroid with pachyvessels and subretinal and intraretinal hyperreflective foci were noted. Fundus autofluorescence (FAF) of the right eye was unremarkable. In the left eye, hyperautofluorescence was seen superior to the fovea, tracking downwards and resembling an early gravitational track ([Fig. 1 a]). After 3 months of persistent and increasing SRF volume ([Fig. 2 a, b]), BCVA in the left eye dropped to 6/12, and the patient was listed for half-dose PDT in the left eye. However, due to a lack of availability of verteporfin, the patient did not receive the treatment for the next 6 months. Meanwhile, the BCVA in the left eye dropped to 6/30, causing the patient to become very upset due to the worsening of visual function. Consequently, he decided to proceed with FLP. The FLP treatment was conducted using a 577 nm laser (Supra Scan 577; Quantel Medical, Cournon dʼAuvergne, France), applying 3 laser spots on and around the area of the leaking PED (300 mW, 200 µm, 0.1 s) to obtain a greyish response on the retina. One month after the FLP treatment, complete SRF resolution was obtained ([Fig. 2 c, d]), along with significant subjective vision improvement and an objective BCVA improvement to 6/12. On FAF, hypoautofluorescence at the fovea resolved with the resolution of SRF, and an enlarged area of hypoautofluorescence was observed at the site of the FLP treatment ([Fig. 1 b]). Fundus examination in the left eye revealed a tiny area of retinal atrophy where FLP was performed. The patient reported no visual field defects.

Zoom Image
Fig. 1 Fundus autofluorescence images before and after focal laser photocoagulation (FLP) treatment. a FAF prior to treatment shows hyperautofluorescence superior to the fovea, tracking downwards and resembling an early gravitational track. An area of hypoautofluorescence around the fovea corresponds to the subretinal fluid. b FAF captured 1 month post-FLP treatment reveals the resolution of both the subretinal fluid and hypoautofluorescence, with an enlarged area of hypoautofluorescence at the site of the FLP treatment.
Zoom Image
Fig. 2 Optical coherence tomography (OCT) showing subretinal fluid (SRF) accumulation and disruption of the outer retinal layers under the fovea (a), and perifoveal superior pigment epithelium detachment (PED) just before focal laser photocoagulation (b). OCT images taken 1 month after the treatment show complete SRF reabsorption under the fovea (c) and around the leaking PED (d).

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Discussion

While FLP is not a novel approach and was the initial treatment method for CSC, its efficacy, simplicity, patient friendliness, and good safety profile are often overlooked by clinicians. In our presented case, we successfully treated the patient with FLP in one session with no need for angiography. Our patient experienced 4 previous episodes of CSC, all of which resolved spontaneously within 2 – 3 months. Despite quick spontaneous resolution of SRF, RPE changes observed on FAF were most likely associated with previous CSC episodes ([Fig. 1 a]). Given the history of spontaneous resolution within 2 – 3 months, we initially opted for observation only during the first 3 months. However, in this instance, SRF under the fovea persisted for 9 months and was accompanied by significant objective and subjective vision loss. Therefore, the patient was very keen to proceed with treatment. Regarding its mechanism of action, FLP acts to seal the area that leaks, which is most commonly associated with RPE irregularities and leaking PED [15]. Experimental studies indicate that adjacent RPE cells expand to cover the gaps created by laser treatment, restoring the RPE barrier [16]. When comparing a cohort of CSC patients after FLP treatment to those following the natural course of CSC, the authors observed a more rapid resolution [5], [17], [18] and a lower likelihood of recurrence in the treated patients [19]. Only two small prospective studies have compared FLP and PDT in patients with chronic CSC. These studies showed faster SRF resolution in the PDT cohort but similar long-term morphological and functional outcomes [20], [21]. Both studies involved patients with chronic CSC and diffuse leakage, in which FLP may be less effective than PDT [20], [21]. We believe that since FLP targets the RPE, ideal candidates for effective FLP treatment should have only focal leakage that is at least one disc diameter away from the fovea. On the other hand, because PDT targets choroidal hyperpermeability, it is effective for both focal and diffuse leakage, and can be applied irrespective of whether the leakage is foveal or extrafoveal [7], [9], [11]. Thus, only future studies that include CSC patients with extrafoveal focal leakage will ascertain the efficacy of FLP compared to the natural course or PDT. In our patient, FLP was performed in less than 5 minutes, with 3 laser spots applied on and around the area of the PED, without FA or indocyanine green angiography (ICGA) prior to treatment. Several clues suggested that the treated PED was the source of SRF leakage beneath the neurosensory retina without confirmation with angiography. In CSC, leakage into the subretinal space is typically associated with RPE irregularities and PED, and given our patient had just one PED, it was likely the leakage source. Additionally, the anatomical location of the PED at the upper margin of the neurosensory detachment suggests that gravitational force contributed to the inferior accumulation of SRF. Furthermore, our patient had a pachyvessel beneath the PED and subretinal hyperreflective material surrounding the PED, both of which are also linked to the area of leakage in CSC [1], [22], [23]. Therefore, considering all indirect indicators of leakage, some CSC patients may not require angiography before FLP treatment, streamlining the treatment planning process. In our case, due to previously confirmed CSC episodes, FA and ICGA were not utilized for establishing the diagnosis and treatment planning. Nevertheless, FA and ICGA continue to be important imaging modalities to establish the diagnosis of CSC. In terms of the safety profile, prior studies have reported scotoma and secondary CNV in CSC patients following FLP treatment [1], [7], [15], [24]. Scotoma after FLP develops due to laser photocoagulation of the PED, which leads to focal atrophy of the outer retinal layers ([Fig. 2 d]). A natural history study of PED in CSC indicated that the majority of PEDs spontaneously resolve, with subsequent RPE atrophy developing in 86% of previous PEDs [25]. Hence, CSC patients are likely to develop a scotoma related to outer retinal layer atrophy, whether or not they undergo FLP treatment. Iatrogenic CNV following FLP in CSC is very rare, being reported in only 11 of 1824 treated eyes (0.60%) [26]. Most reports of iatrogenic CNV following FLP in CSC date back a few decades, when treatments were administered using older generations of laser machines, which may have been more susceptible to inducing iatrogenic CNV. Furthermore, those reports did not utilize newer multimodal imaging techniques like OCT and OCT angiography, which can detect subtle CNV before FLP [27]. At the time, it was not widely recognized that secondary CNV is associated with chronic CSC in 24% of cases, as documented by Mrejen et al. [4]. As a result, CNV might have been erroneously attributed to FLP treatment rather than the natural progression in chronic CSC patients. Retinal laser photocoagulation is widely used in everyday medical retina practice, primarily for treating diabetic retinopathy and retinal vein occlusions. Therefore, FLP for selected patients with CSC could potentially be more widely available and cost-effective, as it eliminates the need for drugs required in treatments like PDT. On the other hand, PDT is usually done only in bigger academic centers with a small number of retinal specialists performing it. Moreover, since July 2021, there has been a global shortage of verteporfin, a critical drug used for PDT [14]. Considering global challenges with verteporfin shortages, limited access to PDT-trained centers, and suboptimal outcomes with other modalities, FLP emerges as a promising option for CSC patients with extrafoveal leakage. Unfortunately, CSC patients with extrafoveal leakage, who could be effectively treated with FLP, are frequently just observed by retinal clinicians, with fluctuating SRF and steady but progressive irreversible vision worsening. Despite focal laser photocoagulationʼs historical presence in CSC treatment, our case serves as a pertinent reminder for retinal specialists to reconsider this treatment approach.


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Conflict of Interest

The authors declare that they have no conflict of interest.

  • References

  • 1 Daruich A, Matet A, Dirani A. et al. Central serous chorioretinopathy: Recent findings and new physiopathology hypothesis. Prog Retin Eye Res 2015; 48: 82-118 DOI: 10.1016/j.preteyeres.2015.05.003.
  • 2 Wang M, Munch IC, Hasler PW. et al. Central serous chorioretinopathy. Acta Ophthalmol 2008; 86: 126-145 DOI: 10.1111/j.1600-0420.2007.00889.x.
  • 3 Kiraly P, Smrekar J, Mekjavić PJ. Visual function during and after an acute central serous chorioretinopathy episode. Doc Ophthalmol 2022; 145: 27-35 DOI: 10.1007/s10633-022-09875-x.
  • 4 Mrejen S, Balaratnasingam C, Kaden TR. et al. Long-term Visual Outcomes and Causes of Vision Loss in Chronic Central Serous Chorioretinopathy. Ophthalmology 2019; 126: 576-588 DOI: 10.1016/j.ophtha.2018.12.048.
  • 5 Burumcek E, Mudun A, Karacorlu S. et al. Laser photocoagulation for persistent central serous retinopathy: results of long-term follow-up. Ophthalmology 1997; 104: 616-622 DOI: 10.1016/s0161-6420(97)30262-0.
  • 6 Slusher MM. Krypton red laser photocoagulation in selected cases of central serous chorioretinopathy. Retina 1986; 6: 81-84 DOI: 10.1097/00006982-198600620-00003.
  • 7 van Rijssen TJ, van Dijk EHC, Yzer S. et al. Central serous chorioretinopathy: Towards an evidence-based treatment guideline. Prog Retin Eye Res 2019; 73: 100770 DOI: 10.1016/j.preteyeres.2019.07.003.
  • 8 Yap EY, Robertson DM. The long-term outcome of central serous chorioretinopathy. Arch Ophthalmol 1996; 114: 689-692 DOI: 10.1001/archopht.1996.01100130681007.
  • 9 van Dijk EHC, Fauser S, Breukink MB. et al. Half-Dose Photodynamic Therapy versus High-Density Subthreshold Micropulse Laser Treatment in Patients with Chronic Central Serous Chorioretinopathy: The PLACE Trial. Ophthalmology 2018; 125: 1547-1555 DOI: 10.1016/j.ophtha.2018.04.021.
  • 10 Bousquet E, Zhao M, Daruich A. et al. Mineralocorticoid antagonists in the treatment of central serous chorioretinopathy: Review of the pre-clinical and clinical evidence. Exp Eye Res 2019; 187: 107754 DOI: 10.1016/j.exer.2019.107754.
  • 11 van Rijssen TJ, van Dijk EHC, Tsonaka R. et al. Half-Dose Photodynamic Therapy Versus Eplerenone in Chronic Central Serous Chorioretinopathy (SPECTRA): A Randomized Controlled Trial. Am J Ophthalmol 2022; 233: 101-110 DOI: 10.1016/j.ajo.2021.06.020.
  • 12 Lotery A, Sivaprasad S, OʼConnell A. et al. Eplerenone for chronic central serous chorioretinopathy in patients with active, previously untreated disease for more than 4 months (VICI): a randomised, double-blind, placebo-controlled trial. Lancet 2020; 395: 294-303 DOI: 10.1016/s0140-6736(19)32981-2.
  • 13 Raizada K, Naik M. Photodynamic Therapy for the Eye. Treasure Island (FL): StatPearls Publishing; 2023
  • 14 Sirks MJ, van Dijk EHC, Rosenberg N. et al. Clinical impact of the worldwide shortage of verteporfin (Visudyne) on ophthalmic care. Acta Ophthalmol 2022; 100: e1522-e1532 DOI: 10.1111/aos.15148.
  • 15 Battaglia Parodi M, Arrigo A, Iacono P. et al. Central Serous Chorioretinopathy: Treatment with Laser. Pharmaceuticals (Basel) 2020; 13: 359 DOI: 10.3390/ph13110359.
  • 16 Inomata H. Wound healing after xenon arc photocoagulation in the rabbit retina. Identification of the proliferating cells in the lesion by light and electron microscopic autoradiography using 3 h-tymidine. Ophthalmologica 1975; 170: 462-474 DOI: 10.1159/000307253.
  • 17 Leaver P, Williams C. Argon laser photocoagulation in the treatment of central serous retinopathy. Br J Ophthalmol 1979; 63: 674-677 DOI: 10.1136/bjo.63.10.674.
  • 18 Khosla PK, Rana SS, Tewari HK. et al. Evaluation of visual function following argon laser photocoagulation in central serous retinopathy. Ophthalmic Surg Lasers 1997; 28: 693-697
  • 19 Robertson DM, Ilstrup D. Direct, indirect, and sham laser photocoagulation in the management of central serous chorioretinopathy. Am J Ophthalmol 1983; 95: 457-466 DOI: 10.1016/0002-9394(83)90265-9.
  • 20 Lim JW, Kang SW, Kim YT. et al. Comparative study of patients with central serous chorioretinopathy undergoing focal laser photocoagulation or photodynamic therapy. Br J Ophthalmol 2011; 95: 514-517 DOI: 10.1136/bjo.2010.182121.
  • 21 Russo A, Turano R, Morescalchi F. et al. Comparison of half-dose photodynamic therapy and 689 nm laser treatment in eyes with chronic central serous chorioretinopathy. Graefes Arch Clin Exp Ophthalmol 2017; 255: 1141-1148 DOI: 10.1007/s00417-017-3626-9.
  • 22 van Dijk EHC, Boon CJF. Serous business: Delineating the broad spectrum of diseases with subretinal fluid in the macula. Prog Retin Eye Res 2021; 84: 100955 DOI: 10.1016/j.preteyeres.2021.100955.
  • 23 Fernández-Vigo JI, Rego-Lorca D, Moreno-Morillo FJ. et al. Intervortex Venous Anastomosis in the Macula in Central Serous Chorioretinopathy Imaged by En Face Optical Coherence Tomography. J Clin Med 2023; 12: 2088 DOI: 10.3390/jcm12062088.
  • 24 Singh SR, Goté JT, Chhablani J. Randomized controlled trials in central serous chorioretinopathy: A review. Eye (Lond) 2023; 37: 3306-3312 DOI: 10.1038/s41433-023-02509-9.
  • 25 Mudvari SS, Goff MJ, Fu AD. et al. The natural history of pigment epithelial detachment associated with central serous chorioretinopathy. Retina 2007; 27: 1168-1173 DOI: 10.1097/IAE.0b013e318156db8a.
  • 26 Matsunaga H, Nangoh K, Uyama M. et al. [Occurrence of choroidal neovascularization following photocoagulation treatment for central serous retinopathy]. Nihon Ganka Gakkai Zasshi 1995; 99: 460-468
  • 27 Schatz H, Yannuzzi LA, Gitter KA. Subretinal neovascularization following argon laser photocoagulation treatment for central serous chorioretinopathy: complication or misdiagnosis? 1975. Retina 2012; 32 (Suppl. 1) OP893-OP906 DOI: 10.1097/iae.0b013e318242fa2d.

Correspondence

PhD Dr. Peter Kiraly
Oxford Eye Hospital
Oxford University Hospitals NHS Foundation Trust
John Radcliffe Hospital, Headley Way
OX3 9DU Oxford
United Kingdom of Great Britain and Northern Ireland   
Phone: + 44 78 21 20 12 05   

Publication History

Received: 19 October 2023

Accepted: 10 December 2023

Accepted Manuscript online:
12 December 2023

Article published online:
14 February 2024

© 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

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Rüdigerstraße 14, 70469 Stuttgart, Germany

  • References

  • 1 Daruich A, Matet A, Dirani A. et al. Central serous chorioretinopathy: Recent findings and new physiopathology hypothesis. Prog Retin Eye Res 2015; 48: 82-118 DOI: 10.1016/j.preteyeres.2015.05.003.
  • 2 Wang M, Munch IC, Hasler PW. et al. Central serous chorioretinopathy. Acta Ophthalmol 2008; 86: 126-145 DOI: 10.1111/j.1600-0420.2007.00889.x.
  • 3 Kiraly P, Smrekar J, Mekjavić PJ. Visual function during and after an acute central serous chorioretinopathy episode. Doc Ophthalmol 2022; 145: 27-35 DOI: 10.1007/s10633-022-09875-x.
  • 4 Mrejen S, Balaratnasingam C, Kaden TR. et al. Long-term Visual Outcomes and Causes of Vision Loss in Chronic Central Serous Chorioretinopathy. Ophthalmology 2019; 126: 576-588 DOI: 10.1016/j.ophtha.2018.12.048.
  • 5 Burumcek E, Mudun A, Karacorlu S. et al. Laser photocoagulation for persistent central serous retinopathy: results of long-term follow-up. Ophthalmology 1997; 104: 616-622 DOI: 10.1016/s0161-6420(97)30262-0.
  • 6 Slusher MM. Krypton red laser photocoagulation in selected cases of central serous chorioretinopathy. Retina 1986; 6: 81-84 DOI: 10.1097/00006982-198600620-00003.
  • 7 van Rijssen TJ, van Dijk EHC, Yzer S. et al. Central serous chorioretinopathy: Towards an evidence-based treatment guideline. Prog Retin Eye Res 2019; 73: 100770 DOI: 10.1016/j.preteyeres.2019.07.003.
  • 8 Yap EY, Robertson DM. The long-term outcome of central serous chorioretinopathy. Arch Ophthalmol 1996; 114: 689-692 DOI: 10.1001/archopht.1996.01100130681007.
  • 9 van Dijk EHC, Fauser S, Breukink MB. et al. Half-Dose Photodynamic Therapy versus High-Density Subthreshold Micropulse Laser Treatment in Patients with Chronic Central Serous Chorioretinopathy: The PLACE Trial. Ophthalmology 2018; 125: 1547-1555 DOI: 10.1016/j.ophtha.2018.04.021.
  • 10 Bousquet E, Zhao M, Daruich A. et al. Mineralocorticoid antagonists in the treatment of central serous chorioretinopathy: Review of the pre-clinical and clinical evidence. Exp Eye Res 2019; 187: 107754 DOI: 10.1016/j.exer.2019.107754.
  • 11 van Rijssen TJ, van Dijk EHC, Tsonaka R. et al. Half-Dose Photodynamic Therapy Versus Eplerenone in Chronic Central Serous Chorioretinopathy (SPECTRA): A Randomized Controlled Trial. Am J Ophthalmol 2022; 233: 101-110 DOI: 10.1016/j.ajo.2021.06.020.
  • 12 Lotery A, Sivaprasad S, OʼConnell A. et al. Eplerenone for chronic central serous chorioretinopathy in patients with active, previously untreated disease for more than 4 months (VICI): a randomised, double-blind, placebo-controlled trial. Lancet 2020; 395: 294-303 DOI: 10.1016/s0140-6736(19)32981-2.
  • 13 Raizada K, Naik M. Photodynamic Therapy for the Eye. Treasure Island (FL): StatPearls Publishing; 2023
  • 14 Sirks MJ, van Dijk EHC, Rosenberg N. et al. Clinical impact of the worldwide shortage of verteporfin (Visudyne) on ophthalmic care. Acta Ophthalmol 2022; 100: e1522-e1532 DOI: 10.1111/aos.15148.
  • 15 Battaglia Parodi M, Arrigo A, Iacono P. et al. Central Serous Chorioretinopathy: Treatment with Laser. Pharmaceuticals (Basel) 2020; 13: 359 DOI: 10.3390/ph13110359.
  • 16 Inomata H. Wound healing after xenon arc photocoagulation in the rabbit retina. Identification of the proliferating cells in the lesion by light and electron microscopic autoradiography using 3 h-tymidine. Ophthalmologica 1975; 170: 462-474 DOI: 10.1159/000307253.
  • 17 Leaver P, Williams C. Argon laser photocoagulation in the treatment of central serous retinopathy. Br J Ophthalmol 1979; 63: 674-677 DOI: 10.1136/bjo.63.10.674.
  • 18 Khosla PK, Rana SS, Tewari HK. et al. Evaluation of visual function following argon laser photocoagulation in central serous retinopathy. Ophthalmic Surg Lasers 1997; 28: 693-697
  • 19 Robertson DM, Ilstrup D. Direct, indirect, and sham laser photocoagulation in the management of central serous chorioretinopathy. Am J Ophthalmol 1983; 95: 457-466 DOI: 10.1016/0002-9394(83)90265-9.
  • 20 Lim JW, Kang SW, Kim YT. et al. Comparative study of patients with central serous chorioretinopathy undergoing focal laser photocoagulation or photodynamic therapy. Br J Ophthalmol 2011; 95: 514-517 DOI: 10.1136/bjo.2010.182121.
  • 21 Russo A, Turano R, Morescalchi F. et al. Comparison of half-dose photodynamic therapy and 689 nm laser treatment in eyes with chronic central serous chorioretinopathy. Graefes Arch Clin Exp Ophthalmol 2017; 255: 1141-1148 DOI: 10.1007/s00417-017-3626-9.
  • 22 van Dijk EHC, Boon CJF. Serous business: Delineating the broad spectrum of diseases with subretinal fluid in the macula. Prog Retin Eye Res 2021; 84: 100955 DOI: 10.1016/j.preteyeres.2021.100955.
  • 23 Fernández-Vigo JI, Rego-Lorca D, Moreno-Morillo FJ. et al. Intervortex Venous Anastomosis in the Macula in Central Serous Chorioretinopathy Imaged by En Face Optical Coherence Tomography. J Clin Med 2023; 12: 2088 DOI: 10.3390/jcm12062088.
  • 24 Singh SR, Goté JT, Chhablani J. Randomized controlled trials in central serous chorioretinopathy: A review. Eye (Lond) 2023; 37: 3306-3312 DOI: 10.1038/s41433-023-02509-9.
  • 25 Mudvari SS, Goff MJ, Fu AD. et al. The natural history of pigment epithelial detachment associated with central serous chorioretinopathy. Retina 2007; 27: 1168-1173 DOI: 10.1097/IAE.0b013e318156db8a.
  • 26 Matsunaga H, Nangoh K, Uyama M. et al. [Occurrence of choroidal neovascularization following photocoagulation treatment for central serous retinopathy]. Nihon Ganka Gakkai Zasshi 1995; 99: 460-468
  • 27 Schatz H, Yannuzzi LA, Gitter KA. Subretinal neovascularization following argon laser photocoagulation treatment for central serous chorioretinopathy: complication or misdiagnosis? 1975. Retina 2012; 32 (Suppl. 1) OP893-OP906 DOI: 10.1097/iae.0b013e318242fa2d.

Zoom Image
Fig. 1 Fundus autofluorescence images before and after focal laser photocoagulation (FLP) treatment. a FAF prior to treatment shows hyperautofluorescence superior to the fovea, tracking downwards and resembling an early gravitational track. An area of hypoautofluorescence around the fovea corresponds to the subretinal fluid. b FAF captured 1 month post-FLP treatment reveals the resolution of both the subretinal fluid and hypoautofluorescence, with an enlarged area of hypoautofluorescence at the site of the FLP treatment.
Zoom Image
Fig. 2 Optical coherence tomography (OCT) showing subretinal fluid (SRF) accumulation and disruption of the outer retinal layers under the fovea (a), and perifoveal superior pigment epithelium detachment (PED) just before focal laser photocoagulation (b). OCT images taken 1 month after the treatment show complete SRF reabsorption under the fovea (c) and around the leaking PED (d).