Successful Management of Familial Exudative Vitreoretinopathy with a Large Macular Hole Using Inverted Internal Limiting Membrane Flap Technique
Abstract Introduction: This case report aims to shed light on a rare presentation of familial exudative vitreoretinopathy (FEVR) co-existing with a large full-thickness macular hole (FTMH) in a 16-year-old male and discuss its successful surgical management, thereby adding to the limited existing kn...
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Published in | Case reports in ophthalmology Vol. 15; no. 1; pp. 129 - 135 |
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Language | English |
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Basel, Switzerland
S. Karger AG
06.02.2024
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Introduction: This case report aims to shed light on a rare presentation of familial exudative vitreoretinopathy (FEVR) co-existing with a large full-thickness macular hole (FTMH) in a 16-year-old male and discuss its successful surgical management, thereby adding to the limited existing knowledge on this topic. Case Presentation: Over an 8-month period, the patient had experienced progressively worsening visual blurring and distortion in his left eye. Following a comprehensive examination, diagnosis confirmed FEVR and an accompanying large FTMH. It was hypothesized that this unusual manifestation resulted from the tractional forces exerted by a thick posterior vitreous membrane and a thin epiretinal membrane – a distinctive attribute of FEVR. The patient underwent surgical intervention, which included pars plana vitrectomy (PPV), internal limiting membrane (ILM) peeling, gas tamponade, and the inverted ILM flap technique. Postoperative outcomes were favorable, with the FTMH successfully closed and substantial improvement observed in the patient’s visual acuity at the 3-month follow-up visit. Conclusion: This case report highlights a rare association of FEVR with FTMH, thereby broadening our understanding of potential complications in patients with FEVR. The successful surgical intervention reinforces the utility of the PPV and the inverted ILM flap technique in managing such complications. It underscores the need for clinicians to maintain vigilance for such atypical manifestations in FEVR patients. |
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AbstractList | This case report aims to shed light on a rare presentation of familial exudative vitreoretinopathy (FEVR) co-existing with a large full-thickness macular hole (FTMH) in a 16-year-old male and discuss its successful surgical management, thereby adding to the limited existing knowledge on this topic.
Over an 8-month period, the patient had experienced progressively worsening visual blurring and distortion in his left eye. Following a comprehensive examination, diagnosis confirmed FEVR and an accompanying large FTMH. It was hypothesized that this unusual manifestation resulted from the tractional forces exerted by a thick posterior vitreous membrane and a thin epiretinal membrane - a distinctive attribute of FEVR. The patient underwent surgical intervention, which included pars plana vitrectomy (PPV), internal limiting membrane (ILM) peeling, gas tamponade, and the inverted ILM flap technique. Postoperative outcomes were favorable, with the FTMH successfully closed and substantial improvement observed in the patient's visual acuity at the 3-month follow-up visit.
This case report highlights a rare association of FEVR with FTMH, thereby broadening our understanding of potential complications in patients with FEVR. The successful surgical intervention reinforces the utility of the PPV and the inverted ILM flap technique in managing such complications. It underscores the need for clinicians to maintain vigilance for such atypical manifestations in FEVR patients. There was no relevant medical history reported among his immediate family members, including his parents and younger brother. Optical coherence tomography angiography and fluorescein angiography of the left eye revealed the presence of linearized retinal vessels and an avascular area accompanied by exudative changes, predominantly located on the temporal side (Fig. 3).Fig. Preoperative optical coherence tomography (OCT) images of the patient's left eye. a and b display horizontal and vertical scans, respectively, showing the presence of a full-thickness macular hole (FTMH). c depicts a wide-field OCT image, clearly demonstrating the thick posterior vitreous membrane (PVM) attached to the edge of the FTMH and the optic disc.Fig. 2. a Preoperative fundus photography of the left eye, demonstrating FTMH (white arrow), accompanied by proliferative vitreoretinopathy and linearized retinal vessels, indicative of familial exudative vitreoretinopathy (FEVR). b Preoperative ultra-wide field fundus photography of the left eye, demonstrating retinal capillary hemangioma in the lower temporal area (white arrow).Fig. In previous reports, to meet the diagnostic criteria for FEVR, patients have to have all 3 of the following: (1) a lack of peripheral retinal vascular development, (2) birth at full term or premature birth with a progression pattern not consistent with the predictable timeline observed in retinopathy of prematurity, and (3) variable degrees of nonperfusion, vitreoretinal traction, subretinal exudation, or retinal neovascularization occurring at any age [7, 8]. Introduction: This case report aims to shed light on a rare presentation of familial exudative vitreoretinopathy (FEVR) co-existing with a large full-thickness macular hole (FTMH) in a 16-year-old male and discuss its successful surgical management, thereby adding to the limited existing knowledge on this topic. Case Presentation: Over an 8-month period, the patient had experienced progressively worsening visual blurring and distortion in his left eye. Following a comprehensive examination, diagnosis confirmed FEVR and an accompanying large FTMH. It was hypothesized that this unusual manifestation resulted from the tractional forces exerted by a thick posterior vitreous membrane and a thin epiretinal membrane – a distinctive attribute of FEVR. The patient underwent surgical intervention, which included pars plana vitrectomy (PPV), internal limiting membrane (ILM) peeling, gas tamponade, and the inverted ILM flap technique. Postoperative outcomes were favorable, with the FTMH successfully closed and substantial improvement observed in the patient’s visual acuity at the 3-month follow-up visit. Conclusion: This case report highlights a rare association of FEVR with FTMH, thereby broadening our understanding of potential complications in patients with FEVR. The successful surgical intervention reinforces the utility of the PPV and the inverted ILM flap technique in managing such complications. It underscores the need for clinicians to maintain vigilance for such atypical manifestations in FEVR patients. Abstract Introduction: This case report aims to shed light on a rare presentation of familial exudative vitreoretinopathy (FEVR) co-existing with a large full-thickness macular hole (FTMH) in a 16-year-old male and discuss its successful surgical management, thereby adding to the limited existing knowledge on this topic. Case Presentation: Over an 8-month period, the patient had experienced progressively worsening visual blurring and distortion in his left eye. Following a comprehensive examination, diagnosis confirmed FEVR and an accompanying large FTMH. It was hypothesized that this unusual manifestation resulted from the tractional forces exerted by a thick posterior vitreous membrane and a thin epiretinal membrane – a distinctive attribute of FEVR. The patient underwent surgical intervention, which included pars plana vitrectomy (PPV), internal limiting membrane (ILM) peeling, gas tamponade, and the inverted ILM flap technique. Postoperative outcomes were favorable, with the FTMH successfully closed and substantial improvement observed in the patient’s visual acuity at the 3-month follow-up visit. Conclusion: This case report highlights a rare association of FEVR with FTMH, thereby broadening our understanding of potential complications in patients with FEVR. The successful surgical intervention reinforces the utility of the PPV and the inverted ILM flap technique in managing such complications. It underscores the need for clinicians to maintain vigilance for such atypical manifestations in FEVR patients. This case report aims to shed light on a rare presentation of familial exudative vitreoretinopathy (FEVR) co-existing with a large full-thickness macular hole (FTMH) in a 16-year-old male and discuss its successful surgical management, thereby adding to the limited existing knowledge on this topic.IntroductionThis case report aims to shed light on a rare presentation of familial exudative vitreoretinopathy (FEVR) co-existing with a large full-thickness macular hole (FTMH) in a 16-year-old male and discuss its successful surgical management, thereby adding to the limited existing knowledge on this topic.Over an 8-month period, the patient had experienced progressively worsening visual blurring and distortion in his left eye. Following a comprehensive examination, diagnosis confirmed FEVR and an accompanying large FTMH. It was hypothesized that this unusual manifestation resulted from the tractional forces exerted by a thick posterior vitreous membrane and a thin epiretinal membrane - a distinctive attribute of FEVR. The patient underwent surgical intervention, which included pars plana vitrectomy (PPV), internal limiting membrane (ILM) peeling, gas tamponade, and the inverted ILM flap technique. Postoperative outcomes were favorable, with the FTMH successfully closed and substantial improvement observed in the patient's visual acuity at the 3-month follow-up visit.Case PresentationOver an 8-month period, the patient had experienced progressively worsening visual blurring and distortion in his left eye. Following a comprehensive examination, diagnosis confirmed FEVR and an accompanying large FTMH. It was hypothesized that this unusual manifestation resulted from the tractional forces exerted by a thick posterior vitreous membrane and a thin epiretinal membrane - a distinctive attribute of FEVR. The patient underwent surgical intervention, which included pars plana vitrectomy (PPV), internal limiting membrane (ILM) peeling, gas tamponade, and the inverted ILM flap technique. Postoperative outcomes were favorable, with the FTMH successfully closed and substantial improvement observed in the patient's visual acuity at the 3-month follow-up visit.This case report highlights a rare association of FEVR with FTMH, thereby broadening our understanding of potential complications in patients with FEVR. The successful surgical intervention reinforces the utility of the PPV and the inverted ILM flap technique in managing such complications. It underscores the need for clinicians to maintain vigilance for such atypical manifestations in FEVR patients.ConclusionThis case report highlights a rare association of FEVR with FTMH, thereby broadening our understanding of potential complications in patients with FEVR. The successful surgical intervention reinforces the utility of the PPV and the inverted ILM flap technique in managing such complications. It underscores the need for clinicians to maintain vigilance for such atypical manifestations in FEVR patients. |
Author | Akada, Masahiro Tabuchi, Hitoshi Nagasawa, Toshihiko |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38322312$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1016/0002-9394(69)91237-9 10.1016/j.ophtha.2015.07.024 10.1080/08820530701418441 10.3928/23258160-20190129-19 10.1016/j.ophtha.2011.06.020 10.1097/ICB.0000000000000613 10.1016/j.ophtha.2013.08.010 10.1016/j.ophtha.2010.02.011 10.1007/s10792-012-9707-1 10.1016/j.ophtha.2013.07.042 10.2147/OPTH.S89683 10.1097/MD.0000000000011048 |
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Keywords | Familial exudative vitreoretinopathy Pars plana vitrectomy Inverted internal limiting membrane flap technique Full-thickness macular hole |
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References | Kashani AH, Learned D, Nudleman E, Drenser KA, Capone A, Trese MT. High prevalence of peripheral retinal vascular anomalies in family members of patients with familial exudative vitreoretinopathy. Ophthalmology. 2014;121(1):262–8. . Yonekawa Y, Thomas BJ, Drenser KA, Trese MT, CaponeAJr. Familial exudative vitreoretinopathy: spectral-domain optical coherence tomography of the vitreoretinal interface, retina, and choroid. Ophthalmology. 2015;122(11):2270–7. . Kimura D, Kobayashi T, Maruyama E, Oosuka S, Kohmoto R, Fukumoto M, . Familial exudative vitreoretinopathy complicated with full thickness macular hole: a case report. Medicine. 2018;97(23):e11048. . Duker JS, Kaiser PK, Binder S, de Smet MD, Gaudric A, Reichel E, . The International Vitreomacular Traction Study Group classification of vitreomacular adhesion, traction, and macular hole. Ophthalmology. 2013;120(12):2611–9. . Munier FL, Daruich A. Macular hole complicating familial exudative vitreoretinopathy due to LRP5 mutation in an adolescent. Ophthalmic Surg Lasers Imaging Retina. 2019;50(2):e49–51. . Shimouchi A, Takahashi A, Nagaoka T, Ishibazawa A, Yoshida A. Vitreomacular interface in patients with familial exudative vitreoretinopathy. Int Ophthalmol. 2013;33(6):711–5. . Criswick VG, Schepens CL. Familial exudative vitreoretinopathy. Am J Ophthalmol. 1969;68(4):578–94. . Khwarg JW, Bourla D, Gonzales CA, Schwartz SD. Familial exudative vitreoretinopathy and macular hole exhibited in same individual. Semin Ophthalmol. 2007;22(2):85–6. . Bochicchio S, Pellegrini M, Cereda M, Oldani M, Staurenghi G. Macular hole in a young patient affected by familial exudative vitreoretinopathy. Retin Cases Brief Rep. 2020;14(1):6–9. . Ranchod TM, Ho LY, Drenser KA, Capone AJr, TreseMT. Clinical presentation of familial exudative vitreoretinopathy. Ophthalmology. 2011;118(10):2070–5. . Ota A, Tanaka Y, Toyoda F, Shimmura M, Kinoshita N, Takano H, . Relationship between variations in posterior vitreous detachment and visual prognosis in idiopathic epiretinal membranes. Clin Ophthalmol. 2016;10:7–11. . Michalewska Z, Michalewski J, Adelman RA, Nawrocki J. Inverted internal limiting membrane flap technique for large macular holes. Ophthalmology. 2010;117(10):2018–25. . ref8 ref7 ref12 ref9 ref4 ref3 ref6 ref11 ref5 ref10 ref2 ref1 |
References_xml | – reference: Ota A, Tanaka Y, Toyoda F, Shimmura M, Kinoshita N, Takano H, . Relationship between variations in posterior vitreous detachment and visual prognosis in idiopathic epiretinal membranes. Clin Ophthalmol. 2016;10:7–11. . – reference: Yonekawa Y, Thomas BJ, Drenser KA, Trese MT, CaponeAJr. Familial exudative vitreoretinopathy: spectral-domain optical coherence tomography of the vitreoretinal interface, retina, and choroid. Ophthalmology. 2015;122(11):2270–7. . – reference: Bochicchio S, Pellegrini M, Cereda M, Oldani M, Staurenghi G. Macular hole in a young patient affected by familial exudative vitreoretinopathy. Retin Cases Brief Rep. 2020;14(1):6–9. . – reference: Ranchod TM, Ho LY, Drenser KA, Capone AJr, TreseMT. Clinical presentation of familial exudative vitreoretinopathy. Ophthalmology. 2011;118(10):2070–5. . – reference: Khwarg JW, Bourla D, Gonzales CA, Schwartz SD. Familial exudative vitreoretinopathy and macular hole exhibited in same individual. Semin Ophthalmol. 2007;22(2):85–6. . – reference: Duker JS, Kaiser PK, Binder S, de Smet MD, Gaudric A, Reichel E, . The International Vitreomacular Traction Study Group classification of vitreomacular adhesion, traction, and macular hole. Ophthalmology. 2013;120(12):2611–9. . – reference: Kimura D, Kobayashi T, Maruyama E, Oosuka S, Kohmoto R, Fukumoto M, . Familial exudative vitreoretinopathy complicated with full thickness macular hole: a case report. Medicine. 2018;97(23):e11048. . – reference: Criswick VG, Schepens CL. Familial exudative vitreoretinopathy. Am J Ophthalmol. 1969;68(4):578–94. . – reference: Kashani AH, Learned D, Nudleman E, Drenser KA, Capone A, Trese MT. High prevalence of peripheral retinal vascular anomalies in family members of patients with familial exudative vitreoretinopathy. Ophthalmology. 2014;121(1):262–8. . – reference: Munier FL, Daruich A. Macular hole complicating familial exudative vitreoretinopathy due to LRP5 mutation in an adolescent. Ophthalmic Surg Lasers Imaging Retina. 2019;50(2):e49–51. . – reference: Shimouchi A, Takahashi A, Nagaoka T, Ishibazawa A, Yoshida A. Vitreomacular interface in patients with familial exudative vitreoretinopathy. Int Ophthalmol. 2013;33(6):711–5. . – reference: Michalewska Z, Michalewski J, Adelman RA, Nawrocki J. Inverted internal limiting membrane flap technique for large macular holes. Ophthalmology. 2010;117(10):2018–25. . – ident: ref1 doi: 10.1016/0002-9394(69)91237-9 – ident: ref2 doi: 10.1016/j.ophtha.2015.07.024 – ident: ref3 doi: 10.1080/08820530701418441 – ident: ref6 doi: 10.3928/23258160-20190129-19 – ident: ref7 doi: 10.1016/j.ophtha.2011.06.020 – ident: ref4 doi: 10.1097/ICB.0000000000000613 – ident: ref8 doi: 10.1016/j.ophtha.2013.08.010 – ident: ref12 doi: 10.1016/j.ophtha.2010.02.011 – ident: ref9 doi: 10.1007/s10792-012-9707-1 – ident: ref10 doi: 10.1016/j.ophtha.2013.07.042 – ident: ref11 doi: 10.2147/OPTH.S89683 – ident: ref5 doi: 10.1097/MD.0000000000011048 |
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Snippet | Abstract
Introduction: This case report aims to shed light on a rare presentation of familial exudative vitreoretinopathy (FEVR) co-existing with a large... Introduction: This case report aims to shed light on a rare presentation of familial exudative vitreoretinopathy (FEVR) co-existing with a large full-thickness... This case report aims to shed light on a rare presentation of familial exudative vitreoretinopathy (FEVR) co-existing with a large full-thickness macular hole... There was no relevant medical history reported among his immediate family members, including his parents and younger brother. Optical coherence tomography... |
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StartPage | 129 |
SubjectTerms | Case Report Case reports familial exudative vitreoretinopathy full-thickness macular hole Hemangioma inverted internal limiting membrane flap technique Medical imaging pars plana vitrectomy Patients Photography Postoperative period Retina Retinal detachment Surgery Tomography Visual acuity |
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Title | Successful Management of Familial Exudative Vitreoretinopathy with a Large Macular Hole Using Inverted Internal Limiting Membrane Flap Technique |
URI | https://karger.com/doi/10.1159/000535714 https://www.ncbi.nlm.nih.gov/pubmed/38322312 https://www.proquest.com/docview/3070509212 https://www.proquest.com/docview/2923326831 https://pubmed.ncbi.nlm.nih.gov/PMC10846875 https://doaj.org/article/a1ba2fe1ca5148fda78b3e4b22c2a1cf |
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