Cargando…
Pregnancy-induced hypertension-related chorioretinitis resembling uveal effusion syndrome: A case report
RATIONALE: Pregnancy-induced hypertension (PIH) is a major cause of maternal and fetal mortality. Hypertensive choroidopathy is a preliminary sign of vasogenic edema in the choroid, and is associated with PIH. Here, we report a post-natal case of PIH-related chorioretinitis with bilateral severe ser...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078765/ https://www.ncbi.nlm.nih.gov/pubmed/30045283 http://dx.doi.org/10.1097/MD.0000000000011572 |
_version_ | 1783345147999682560 |
---|---|
author | Sato, Tomohito Takeuchi, Masaru |
author_facet | Sato, Tomohito Takeuchi, Masaru |
author_sort | Sato, Tomohito |
collection | PubMed |
description | RATIONALE: Pregnancy-induced hypertension (PIH) is a major cause of maternal and fetal mortality. Hypertensive choroidopathy is a preliminary sign of vasogenic edema in the choroid, and is associated with PIH. Here, we report a post-natal case of PIH-related chorioretinitis with bilateral severe serous retinal detachment (SRD) resembling uveal effusion syndrome. PATIENT CONCERNS: A 35-year-old woman was diagnosed with severe PIH at 37 weeks of pregnancy. She underwent an emergency cesarean delivery. Four days after delivery, she perceived a sudden decrease of vision. At presentation, fundus examination demonstrated bullous SRD and multiple white mottles in the posterior poles of both eyes. Optical coherence tomography (OCT) showed macula edema and retinal pigment epithelium (RPE) folds. Indocyanine green angiography (ICGA) demonstrated delayed filling of choroidal circulation in the early phase and multiple hyperfluorescent spots in the mid phase. DIAGNOSES: PIH. INTERVENTIONS: Antihypertension treatment alone resulted in gradual resolution of the SRD. OUTCOMES: At 463 days after delivery, fundus photographs of both eyes showed leopard spots corresponding to hyperautofluorescent spots with dark rim observed on fundus autofluorescence images. LESSONS: Ophthalmologists should be aware of PIH-related chorioretinitis with similar clinical manifestations as uveal effusion syndrome, and should treat with antihypertensive agents in cooperation with obstetricians. |
format | Online Article Text |
id | pubmed-6078765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-60787652018-08-13 Pregnancy-induced hypertension-related chorioretinitis resembling uveal effusion syndrome: A case report Sato, Tomohito Takeuchi, Masaru Medicine (Baltimore) Research Article RATIONALE: Pregnancy-induced hypertension (PIH) is a major cause of maternal and fetal mortality. Hypertensive choroidopathy is a preliminary sign of vasogenic edema in the choroid, and is associated with PIH. Here, we report a post-natal case of PIH-related chorioretinitis with bilateral severe serous retinal detachment (SRD) resembling uveal effusion syndrome. PATIENT CONCERNS: A 35-year-old woman was diagnosed with severe PIH at 37 weeks of pregnancy. She underwent an emergency cesarean delivery. Four days after delivery, she perceived a sudden decrease of vision. At presentation, fundus examination demonstrated bullous SRD and multiple white mottles in the posterior poles of both eyes. Optical coherence tomography (OCT) showed macula edema and retinal pigment epithelium (RPE) folds. Indocyanine green angiography (ICGA) demonstrated delayed filling of choroidal circulation in the early phase and multiple hyperfluorescent spots in the mid phase. DIAGNOSES: PIH. INTERVENTIONS: Antihypertension treatment alone resulted in gradual resolution of the SRD. OUTCOMES: At 463 days after delivery, fundus photographs of both eyes showed leopard spots corresponding to hyperautofluorescent spots with dark rim observed on fundus autofluorescence images. LESSONS: Ophthalmologists should be aware of PIH-related chorioretinitis with similar clinical manifestations as uveal effusion syndrome, and should treat with antihypertensive agents in cooperation with obstetricians. Wolters Kluwer Health 2018-07-27 /pmc/articles/PMC6078765/ /pubmed/30045283 http://dx.doi.org/10.1097/MD.0000000000011572 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | Research Article Sato, Tomohito Takeuchi, Masaru Pregnancy-induced hypertension-related chorioretinitis resembling uveal effusion syndrome: A case report |
title | Pregnancy-induced hypertension-related chorioretinitis resembling uveal effusion syndrome: A case report |
title_full | Pregnancy-induced hypertension-related chorioretinitis resembling uveal effusion syndrome: A case report |
title_fullStr | Pregnancy-induced hypertension-related chorioretinitis resembling uveal effusion syndrome: A case report |
title_full_unstemmed | Pregnancy-induced hypertension-related chorioretinitis resembling uveal effusion syndrome: A case report |
title_short | Pregnancy-induced hypertension-related chorioretinitis resembling uveal effusion syndrome: A case report |
title_sort | pregnancy-induced hypertension-related chorioretinitis resembling uveal effusion syndrome: a case report |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078765/ https://www.ncbi.nlm.nih.gov/pubmed/30045283 http://dx.doi.org/10.1097/MD.0000000000011572 |
work_keys_str_mv | AT satotomohito pregnancyinducedhypertensionrelatedchorioretinitisresemblinguvealeffusionsyndromeacasereport AT takeuchimasaru pregnancyinducedhypertensionrelatedchorioretinitisresemblinguvealeffusionsyndromeacasereport |