We describe focal choroidal excavation (FCE) in a case of Vogt–Koyanagi–Harada (VKH) disease and compare the findings with different chorioretinal conditions. A 55-year-old man was diagnosed with VKH based on panuveitis and exudative retinal detachments. Spectral-domain optical coherence tomography demonstrated a dome-shaped protrusion with a nonconforming pattern at the fovea, which had been detected as a conforming pattern 1 year before the onset. The FCE pattern returned into a conforming pattern following corticosteroid therapy. These findings suggest that the natively existent FCE could be affected by pathophysiological changes of VKH as well as other chorioretinal conditions

Akiyama, K

Fujinami, K

Nishikawa, Y

Noda, T

Tsunoda, K

Watanabe, K

PubMed

UCL Discovery

© 2014 Nishikawa et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0)  License. The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. Permissions beyond the scope of the License are administered by Dove Medical Press Limited. Information on how to request permission may be found at: http://www.dovepress.com/permissions.phpClinical Ophthalmology 2014:8 2461–2465Clinical Ophthalmology Dovepresssubmit your manuscript | www.dovepress.comDovepress 2461C a s e  s e r i e sopen access to scientific and medical researchOpen access Full Text articlehttp://dx.doi.org/10.2147/OPTH.S75558Clinical course of focal choroidal excavation in Vogt–Koyanagi–Harada diseaseYuko Nishikawa1–3,*Kaoru Fujinami1,2,4,5,*Ken Watanabe1,2Toru Noda1,2Kazushige Tsunoda1,2Kunihiko akiyama1,21Department of Ophthalmology, National Hospital Organization, Tokyo Medical Center, Tokyo, Japan; 2Laboratory of Visual Physiology, National institute of sensory Organs, National Tokyo Medical Center, Tokyo, Japan; 3Department of Ophthalmology, Osaka Medical College, Takatsuki, Osaka, Japan; 4Department of Ophthalmology, Keio University school of Medicine, Tokyo, Japan; 5UCL institute of Ophthalmology, London, UK*These authors contributed equally to this workAbstract: We describe focal choroidal excavation (FCE) in a case of Vogt–Koyanagi–Harada (VKH) disease and compare the findings with different chorioretinal conditions. A 55-year-old man was diagnosed with VKH based on panuveitis and exudative retinal detachments. Spectral-domain optical coherence tomography demonstrated a dome-shaped protrusion with a nonconforming pattern at the fovea, which had been detected as a conforming pattern 1 year before the onset. The FCE pattern returned into a conforming pattern following corticosteroid therapy. These findings suggest that the natively existent FCE could be affected by pathophysi-ological changes of VKH as well as other chorioretinal conditions.Keywords: choroidal excavation, focal choroidal excavation, Vogt–Koyanagi–Harada disease, optical coherence tomographyIntroductionFocal choroidal excavation (FCE) was first described by Jampol et al1 as an anomalous excavation of the choroid; it is typically observed by optical coherence tomography (OCT).1,2 This condition has been associated with several chorioretinal conditions and asymptomatic status, including central serous chorioretinopathy, choroidal neovas-cularization, and best vitelliform macular dystrophy.1–12 However, the mechanisms underlying the formation of FCE remain uncertain.Wakabayashi et al2 described two patterns of FCE: 1) conforming pattern – exca-vations that involved the outer retinal layers up to and including the external limiting membrane; and 2) nonconforming pattern – excavations that involved only the retinal pigment epithelium (RPE).Recently, a case report of FCE associated with Vogt–Koyanagi–Harada (VKH) disease has been published,13 which documented cross-sectional observation. Here we describe a clinical course of FCE associated with VKH before and after treat-ment and compare the morphological findings of FCE in four subjects with different chorioretinal conditions.Case reportA 55-year-old man (subject 1) presented with bilateral metamorphopsia, with decimal visual acuity being 0.8 in the right eye and 1.2 in the left. The clinical diagnosis of VKH was made based on bilateral panuveitis and multifocal exudative retinal detachments at the posterior poles (Figure 1). High-dose corticosteroid therapy with gradual taper-ing was initiated 3 days after presentation. The serous detachments entirely resolved within 9 weeks and visual acuity in the right eye improved to 1.2.Serial spectral-domain OCT (SD-OCT) images obtained at the preuveitic, uveitic, and posttreatment phase are shown in Figure 2. SD-OCT obtained 1 year before Correspondence: Kaoru FujinamiLaboratory of Visual Physiology, National institute of sensory Organs, National Tokyo Medical Center, 2-5-1 Higashigaoka, Meguro-ku, Tokyo 152-8902, JapanTel +81 3 3411 0111Fax +81 3 3411 0185email kfj21kfj21kfj21@kmf.biglobe.ne.jp Journal name: Clinical OphthalmologyArticle Designation: Case SeriesYear: 2014Volume: 8Running head verso: Nishikawa et alRunning head recto: Focal choroidal excavation in Vogt–Koyanagi–Harada diseaseDOI: http://dx.doi.org/10.2147/OPTH.S75558Clinical Ophthalmology 2014:8submit your manuscript | www.dovepress.comDovepress Dovepress2462Nishikawa et alPreuveitic phase Uveitic phase pretreatmentUveitic phase pretreatmentUveitic phase posttreatment (9 weeks)Uveitic phase pretreatmentA DEBCFigure 1 Fundus photographs, fluorescein angiograms, and indocyanine green angiograms of a case with Vogt–Koyanagi–Harada disease (subject 1).Notes: (A) Fundus photography at preuveitic phase (1 year before the onset of uveitis) showed subtle RPE disturbance at the fovea in the right eye with normal findings in the left eye. (B) at the onset, fundus photography revealed bilateral multifocal exudative retinal detachments throughout the posterior pole in each eye, with the subtle RPE disturbance unchanged in the right eye. (C) Nine weeks after treatment, the exudative detachments had resolved in each eye. (D) Fluorescein angiography at the onset demonstrated multiple punctate hyperfluorescent lesions and multilobular pools of subretinal dye in each eye. (E) Indocyanine green angiography at the onset identified multiple hypofluorescent spots in each eye with a hyperfluorescent lesion at the superior nasal fovea.Abbreviation: rPe, retinal pigment epithelial.the onset of VKH due to symptoms of a floater and visual disturbance demonstrated a dome-shaped posterior protrusion of the RPE and outer retinal layers into the choroidal cavity (ie, conforming FCE) at the fovea in the right eye. SD-OCT at the uveitic phase identified multiple bilateral sensory retinal detachments, with the FCE now involving only the RPE (ie, nonconforming FCE). Nine weeks after the treatment, the nonconforming FCE returned into a conforming pattern.The FCE pattern and its alteration during treatment of the case with VKH were compared to those of four subjects with FCE associated with other chorioretinal conditions (Figure 3). This comparison group consisted of two patients with age-related macular degeneration (AMD; subjects 2 and 3), one subject with a macular hole (MH; subject 4), and one asymptomatic individual (subject 5). Treatment with intravitreal ranibizumab injections and vitrectomy had been performed in the patients with AMD and MH, respectively. A conforming FCE was observed in three patients (subjects 2, 3, and 5) and pattern alteration from nonconforming to conforming FCE was found after treatment in one subject (subject 4). In the two subjects with AMD, a hyperreflective material around the FCE was absorbed, resulting in a well-demarcated conforming FCE after treatment.DiscussionA detailed clinical course of FCE at the fovea was documented in a case with VKH disease. SD-OCT images obtained at the preuveitic, uveitic, and posttreatment phase suggested the preexistence of FCE before the onset of VKH, and the FCE pattern change (from conforming to nonconforming pattern during the period of choroidal inflammation) was observed during the follow-up.The FCE identified at the preuveitic phase in our case supported the congenital/acquired posterior pole Clinical Ophthalmology 2014:8 submit your manuscript | www.dovepress.comDovepress Dovepress2463Focal choroidal excavation in Vogt–Koyanagi–Harada diseasePreuveitic phaseUveitic phase pretreatmentUveitic phase posttreatment (2 weeks)Uveitic phase posttreatment (9 weeks)ABCDFigure 2 Serial spectral-domain optical coherence tomographic images of a case with Vogt–Koyanagi–Harada disease (subject 1).Notes: (A) Spectral-domain optical coherence tomography at the preuveitic phase (1 year before the onset) showed a dome-shaped posterior protrusion of the hyperreflective bands of the RPE and outer retinal layers into the choroidal cavity (ie, conforming pattern of FCE) at the fovea in the right eye, with normal findings in the left eye (FCE asterisked). (B) At the onset, multiple bilateral sensory retinal detachments were demonstrated in each eye, with the FCE involving only the RPE (ie, nonconforming FCE) (FCE asterisked). (C) Two weeks after treatment, the serous detachments had partially resolved, with residual subretinal fluid at the fovea in each eye, with a nonconforming FCE at the right fovea (FCE asterisked). (D) Nine weeks after treatment, the serous detachments had entirely resolved, resulting in the reappearance of a conforming FCE at the right fovea (FCE asterisked).Abbreviations: FCe, focal choroidal excavation; rPe, retinal pigment epithelium.malformation, as previously suggested.1,4,9,11,12 On the other hand, Hashida et al13 speculated that a direct pressure effect on the choroidal layer by subretinal fibrin disrupted the chor-oidal integrity and focal choroidal atrophy/thinning following inflammation and resulted in a formation of FCE in a case with VKH.4,7,13 Although such a remarkable subretinal fibrin was not detected, the association between the FCE formation and choroidal inflammation could not be excluded entirely in our case, considering other possible subclinical inflammatory events prior to this disease history.Clinical Ophthalmology 2014:8submit your manuscript | www.dovepress.comDovepress Dovepress2464Nishikawa et alSubject 2 age-related macular degeneration, pretreatmentSubject 3 age-related macular degeneration, pretreatmentSubject 4 macular hole, pretreatmentSubject 2 posttreatmentSubject 3 posttreatmentSubject 4 posttreatmentSubject 5 asymptomaticABCDFigure 3 Fundus photographs and spectral-domain optical coherence tomographic images of four cases with focal choroidal excavation (subjects 2, 3, 4, and 5).Notes: (A) Subject 2 (54-year-old man with age-related macular degeneration): Fundus photography at onset showed subtle RPE disturbance at the fovea, and SD-OCT demonstrated an FCE filled with a hyperreflective material (left; FCE asterisked; material arrowed). After treatment with intravitreal ranibizumab injections, a juxtafoveal hypopigmented spot was seen surrounded by RPE disturbance; the hyperreflective material in the FCE had been absorbed and a well-demarcated conforming FCE was observed (right; FCEs asterisked; absorbed material arrowed). (B) Subject 3 (67-year-old man with age-related macular degeneration): Fundus photography at onset revealed subtle RPE disturbance at the fovea surrounded by a hypopigmented area at the macula; SD-OCT detected a FCE and subretinal hyperreflective material above the irregular RPE (left; FCE asterisked; material arrowed). After intravitreal ranibizumab injections, the fundus appearance had not changed and a conforming FCE was clearly observed with the irregular RPE (right; FCE asterisked; absorbed material arrowed). (C) Subject 4 (55-year old woman with macular hole): Fundus photography showed a hyperreflective membrane at the macula with RPE loss at the fovea; SD-OCT demonstrated an impending MH with retinoschisis and a juxtafoveal nonconforming FCE (left; FCE asterisked). After vitrectomy, the MH had sealed following removal of vitreomacular traction and a conforming FCE was observed (left; FCE asterisked). (D) Subject 5 (72-year-old asymptomatic woman): Fundus photography revealed no abnormalities and SD-OCT detected conforming FCEs at the fovea (left; FCEs asterisked).Abbreviations: FCe, focal choroidal excavation; MH, macular hole; rPe, retinal pigment epithelium; sD-OCT, spectral-domain optical coherence tomography.An alteration of the FCE pattern observed in VKH was also found in the comparison group with other chorioretinal conditions. In subject 4 with an MH, the nonconforming FCE at presentation associated with vitreomacular traction changed to conforming FCE after treatment. In two subjects with AMD, a hyperreflective material around the FCE was observed to be absorbed, resulting in a well-demarcated conforming FCE via treatment (subjects 2 and 3). These findings suggest that the cavity within FCE can be filled with subretinal fluid associated with inflammation and exu-dative material generated by choroidal neovascularization. The decreased adhesion within the FCE between RPE and photoreceptor could complicate MHs. Given the proximity between the FCE and the active lesions, the involved retina around the active lesion may well show disorganization of retinal layers in the pathological process; then the conforming pattern is hard to maintain, unsurprisingly. In addition, it is possible that the cavity within FCE may potentially accelerate the pathophysiological changes of chorioretinal disorders.AcknowledgmentsThis research was supported in part by research grants from the Ministry of Health, Labor and Welfare, Japan and Grant-in-Aid for Scientific Research from Japan Society for the Clinical OphthalmologyPublish your work in this journalSubmit your manuscript here: http://www.dovepress.com/clinical-ophthalmology-journalClinical Ophthalmology is an international, peer-reviewed journal covering all subspecialties within ophthalmology. Key topics include: Optometry; Visual science; Pharmacology and drug therapy in eye diseases; Basic Sciences; Primary and Secondary eye care; Patient Safety and Quality of Care Improvements. This journal is indexed on PubMed Central and CAS, and is the official journal of The Society of Clinical Ophthalmology (SCO). The manuscript management system is completely online and includes a very quick and fair peer-review system, which is all easy to use. Visit http://www.dovepress.com/testimonials.php to read real quotes from published authors.Clinical Ophthalmology 2014:8 submit your manuscript | www.dovepress.comDovepress DovepressDovepress2465Focal choroidal excavation in Vogt–Koyanagi–Harada diseasePromotion of Science. KF is supported by a Grant-in-Aid for Young Scientists (B) of the Ministry of Education, Culture, Sports, Science and Technology (Japan). The sponsor or funding organization had no role in the design or conduct of this research.DisclosureThe authors have no proprietary or commercial interest in any materials discussed in this article. The authors report no other conflicts of interest in this work.References1. Jampol LM, Shankle J, Schroeder R, Tornambe P, Spaide RF, Hee MR. Diagnostic and therapeutic challenges. Retina. 2006;26(9):1072–1076.2. 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Clinical course of focal choroidal excavation in Vogt-Koyanagi-Harada disease

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