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Case report: Sympathetic ophthalmia after vitrectomies in a patient with Von Hippel–Lindau syndrome

BACKGROUND: Sympathetic ophthalmia (SO) is a rare but sight-threatening uveitis, and most observations have been made after typical manifestations occur. This report focuses on the choroidal changes detected by multimodal imaging at the presymptomatic stage of SO, which is implicated in the early re...

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Autores principales: Zhuang, Xiaonan, Gao, Fengjuan, Sun, Zhongcui, Ding, Xinyi, Xu, Gezhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968801/
https://www.ncbi.nlm.nih.gov/pubmed/36860339
http://dx.doi.org/10.3389/fmed.2023.1118913
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author Zhuang, Xiaonan
Gao, Fengjuan
Sun, Zhongcui
Ding, Xinyi
Xu, Gezhi
author_facet Zhuang, Xiaonan
Gao, Fengjuan
Sun, Zhongcui
Ding, Xinyi
Xu, Gezhi
author_sort Zhuang, Xiaonan
collection PubMed
description BACKGROUND: Sympathetic ophthalmia (SO) is a rare but sight-threatening uveitis, and most observations have been made after typical manifestations occur. This report focuses on the choroidal changes detected by multimodal imaging at the presymptomatic stage of SO, which is implicated in the early recognition of SO. CASE PRESENTATION: A 21-year-old woman suffered from decreased vision in the right eye and was diagnosed with retinal capillary hemangioblastomas associated with Von Hippel–Lindau syndrome. The patient underwent two 23-G pars plana vitrectomies (PPVs), soon after which typical signs of SO manifested. SO resolved quickly after the oral administration of prednisone and remained stable during the follow-up of more than 1 year. The retrospective analysis revealed preexisting bilaterally increased choroidal thickness, dots of flow void on the choroid, and choriocapillaris en-face slabs in optical coherence tomography angiography (OCTA) after the first PPV, which were all reversed by corticosteroid treatment. CONCLUSION: The case report highlights the involvement of the choroid and choriocapillaris at the presymptomatic stage of SO after the first inciting event. Abnormally thickened choroid and flow void dots suggested that SO had started and an ensuing surgery would run the risk of exacerbating SO. OCTA scanning of both eyes should be ordered routinely for patients with a history of trauma or intraocular surgeries, especially before the next surgical intervention. The report also suggests that non-human leukocyte antigen gene variation may also regulate the progression of SO, which requires further laboratory investigations.
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spelling pubmed-99688012023-02-28 Case report: Sympathetic ophthalmia after vitrectomies in a patient with Von Hippel–Lindau syndrome Zhuang, Xiaonan Gao, Fengjuan Sun, Zhongcui Ding, Xinyi Xu, Gezhi Front Med (Lausanne) Medicine BACKGROUND: Sympathetic ophthalmia (SO) is a rare but sight-threatening uveitis, and most observations have been made after typical manifestations occur. This report focuses on the choroidal changes detected by multimodal imaging at the presymptomatic stage of SO, which is implicated in the early recognition of SO. CASE PRESENTATION: A 21-year-old woman suffered from decreased vision in the right eye and was diagnosed with retinal capillary hemangioblastomas associated with Von Hippel–Lindau syndrome. The patient underwent two 23-G pars plana vitrectomies (PPVs), soon after which typical signs of SO manifested. SO resolved quickly after the oral administration of prednisone and remained stable during the follow-up of more than 1 year. The retrospective analysis revealed preexisting bilaterally increased choroidal thickness, dots of flow void on the choroid, and choriocapillaris en-face slabs in optical coherence tomography angiography (OCTA) after the first PPV, which were all reversed by corticosteroid treatment. CONCLUSION: The case report highlights the involvement of the choroid and choriocapillaris at the presymptomatic stage of SO after the first inciting event. Abnormally thickened choroid and flow void dots suggested that SO had started and an ensuing surgery would run the risk of exacerbating SO. OCTA scanning of both eyes should be ordered routinely for patients with a history of trauma or intraocular surgeries, especially before the next surgical intervention. The report also suggests that non-human leukocyte antigen gene variation may also regulate the progression of SO, which requires further laboratory investigations. Frontiers Media S.A. 2023-02-13 /pmc/articles/PMC9968801/ /pubmed/36860339 http://dx.doi.org/10.3389/fmed.2023.1118913 Text en Copyright © 2023 Zhuang, Gao, Sun, Ding and Xu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Zhuang, Xiaonan
Gao, Fengjuan
Sun, Zhongcui
Ding, Xinyi
Xu, Gezhi
Case report: Sympathetic ophthalmia after vitrectomies in a patient with Von Hippel–Lindau syndrome
title Case report: Sympathetic ophthalmia after vitrectomies in a patient with Von Hippel–Lindau syndrome
title_full Case report: Sympathetic ophthalmia after vitrectomies in a patient with Von Hippel–Lindau syndrome
title_fullStr Case report: Sympathetic ophthalmia after vitrectomies in a patient with Von Hippel–Lindau syndrome
title_full_unstemmed Case report: Sympathetic ophthalmia after vitrectomies in a patient with Von Hippel–Lindau syndrome
title_short Case report: Sympathetic ophthalmia after vitrectomies in a patient with Von Hippel–Lindau syndrome
title_sort case report: sympathetic ophthalmia after vitrectomies in a patient with von hippel–lindau syndrome
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968801/
https://www.ncbi.nlm.nih.gov/pubmed/36860339
http://dx.doi.org/10.3389/fmed.2023.1118913
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