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Case of catastrophic antiphospholipid syndrome presenting as neuroretinitis and vaso-occlusive retinopathy
BACKGROUND: Ocular involvement in catastrophic antiphospholipid syndrome (CAPS), a rare, life-threatening form of antiphospholipid syndrome (APS) that results in multiorgan failure and a high mortality rate, has rarely been reported. CASE PRESENTATION: A 15-year-old girl presented with sudden vision...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727181/ https://www.ncbi.nlm.nih.gov/pubmed/33298003 http://dx.doi.org/10.1186/s12886-020-01755-9 |
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author | In Yun, Young Kim, Ji Hyun Lim, Seon Hee Ahn, Yo Han Kang, Hee Gyung Ha, Il-Soo Oh, Baek-Lok |
author_facet | In Yun, Young Kim, Ji Hyun Lim, Seon Hee Ahn, Yo Han Kang, Hee Gyung Ha, Il-Soo Oh, Baek-Lok |
author_sort | In Yun, Young |
collection | PubMed |
description | BACKGROUND: Ocular involvement in catastrophic antiphospholipid syndrome (CAPS), a rare, life-threatening form of antiphospholipid syndrome (APS) that results in multiorgan failure and a high mortality rate, has rarely been reported. CASE PRESENTATION: A 15-year-old girl presented with sudden vision blurring in both eyes. She had marked optic disc swelling and macular exudates in the right eye and intra-arterial white plaques, a few retinal blot hemorrhages, and a white ischemic retina in the left eye. Systemic examination revealed she had acute kidney injury with thrombotic microangiopathy (TMA), multiple cerebral infarcts, valvular dysfunction, and a high titer of triple aPL. Thus, she was diagnosed with CAPS involving the brain, eyes, heart, and kidneys. Plasma exchange and the administration of glucocorticoids, immunoglobulin, warfarin, and rituximab brought a sustained recovery of the TMA, visual symptoms, and echocardiographic findings. CONCLUSIONS: Ocular involvement of both vaso-occlusive retinopathy, an APS-related thrombotic microangiopathy, and neuroretinitis, a non-thrombotic microangiopathy, can occur as an initial presentation of CAPS. |
format | Online Article Text |
id | pubmed-7727181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77271812020-12-11 Case of catastrophic antiphospholipid syndrome presenting as neuroretinitis and vaso-occlusive retinopathy In Yun, Young Kim, Ji Hyun Lim, Seon Hee Ahn, Yo Han Kang, Hee Gyung Ha, Il-Soo Oh, Baek-Lok BMC Ophthalmol Case Report BACKGROUND: Ocular involvement in catastrophic antiphospholipid syndrome (CAPS), a rare, life-threatening form of antiphospholipid syndrome (APS) that results in multiorgan failure and a high mortality rate, has rarely been reported. CASE PRESENTATION: A 15-year-old girl presented with sudden vision blurring in both eyes. She had marked optic disc swelling and macular exudates in the right eye and intra-arterial white plaques, a few retinal blot hemorrhages, and a white ischemic retina in the left eye. Systemic examination revealed she had acute kidney injury with thrombotic microangiopathy (TMA), multiple cerebral infarcts, valvular dysfunction, and a high titer of triple aPL. Thus, she was diagnosed with CAPS involving the brain, eyes, heart, and kidneys. Plasma exchange and the administration of glucocorticoids, immunoglobulin, warfarin, and rituximab brought a sustained recovery of the TMA, visual symptoms, and echocardiographic findings. CONCLUSIONS: Ocular involvement of both vaso-occlusive retinopathy, an APS-related thrombotic microangiopathy, and neuroretinitis, a non-thrombotic microangiopathy, can occur as an initial presentation of CAPS. BioMed Central 2020-12-09 /pmc/articles/PMC7727181/ /pubmed/33298003 http://dx.doi.org/10.1186/s12886-020-01755-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report In Yun, Young Kim, Ji Hyun Lim, Seon Hee Ahn, Yo Han Kang, Hee Gyung Ha, Il-Soo Oh, Baek-Lok Case of catastrophic antiphospholipid syndrome presenting as neuroretinitis and vaso-occlusive retinopathy |
title | Case of catastrophic antiphospholipid syndrome presenting as neuroretinitis and vaso-occlusive retinopathy |
title_full | Case of catastrophic antiphospholipid syndrome presenting as neuroretinitis and vaso-occlusive retinopathy |
title_fullStr | Case of catastrophic antiphospholipid syndrome presenting as neuroretinitis and vaso-occlusive retinopathy |
title_full_unstemmed | Case of catastrophic antiphospholipid syndrome presenting as neuroretinitis and vaso-occlusive retinopathy |
title_short | Case of catastrophic antiphospholipid syndrome presenting as neuroretinitis and vaso-occlusive retinopathy |
title_sort | case of catastrophic antiphospholipid syndrome presenting as neuroretinitis and vaso-occlusive retinopathy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727181/ https://www.ncbi.nlm.nih.gov/pubmed/33298003 http://dx.doi.org/10.1186/s12886-020-01755-9 |
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