Subfoveal Choroidal Neovascular Membrane Secondary to Idiopathic Intracranial Hypertension
Purpose: To present a rare case of subfoveal choroidal neovascular membrane (CNVM) secondary to idiopathic intracranial hypertension. Methods: A case was evaluated. Results: A 21-year-old woman presented with a 2-week history of painless blurred vision in the right eye. She described initial metamor...
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Veröffentlicht in: | Journal of vitreoretinal diseases (Print) 2024-03, Vol.8 (2), p.192-195 |
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creator | Pereira, Austin Nichani, Prem A.H. Yan, Peng Micieli, Jonathan A. |
description | Purpose: To present a rare case of subfoveal choroidal neovascular membrane (CNVM) secondary to idiopathic intracranial hypertension. Methods: A case was evaluated. Results: A 21-year-old woman presented with a 2-week history of painless blurred vision in the right eye. She described initial metamorphopsia and intermittent bitemporal headaches lasting 30 minutes. She denied pain with eye movements and a history of trauma. Her body mass index was 49 kg/m2. The visual acuity (VA) was 20/320 OD and 20/20 OS; there was no relative afferent pupillary defect. A dilated fundus examination showed bilateral optic disc edema and a subfoveal CNVM in the right eye. The patient was started on oral acetazolamide 500 mg twice daily and treated with 2 intravitreal antivascular endothelial growth factor (anti-VEGF) injections. Three months later, the VA was 20/30 in the right eye and the disc edema had improved. Conclusions: CNVMs in the setting of idiopathic intracranial hypertension–related papilledema may be subfoveal and have an excellent response to anti-VEGF agents. |
doi_str_mv | 10.1177/24741264231218539 |
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Methods: A case was evaluated. Results: A 21-year-old woman presented with a 2-week history of painless blurred vision in the right eye. She described initial metamorphopsia and intermittent bitemporal headaches lasting 30 minutes. She denied pain with eye movements and a history of trauma. Her body mass index was 49 kg/m2. The visual acuity (VA) was 20/320 OD and 20/20 OS; there was no relative afferent pupillary defect. A dilated fundus examination showed bilateral optic disc edema and a subfoveal CNVM in the right eye. The patient was started on oral acetazolamide 500 mg twice daily and treated with 2 intravitreal antivascular endothelial growth factor (anti-VEGF) injections. Three months later, the VA was 20/30 in the right eye and the disc edema had improved. Conclusions: CNVMs in the setting of idiopathic intracranial hypertension–related papilledema may be subfoveal and have an excellent response to anti-VEGF agents.</description><identifier>ISSN: 2474-1264</identifier><identifier>EISSN: 2474-1272</identifier><identifier>DOI: 10.1177/24741264231218539</identifier><identifier>PMID: 38465349</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Case Reports</subject><ispartof>Journal of vitreoretinal diseases (Print), 2024-03, Vol.8 (2), p.192-195</ispartof><rights>The Author(s) 2023</rights><rights>The Author(s) 2023.</rights><rights>The Author(s) 2023 2023 American Society of Retina Specialists</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c358t-5727a512b2e8188389d2560e5bb20da2c4887793f6b0fa4f154a10fa86c3071c3</cites><orcidid>0000-0003-3818-9788</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/24741264231218539$$EPDF$$P50$$Gsage$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/24741264231218539$$EHTML$$P50$$Gsage$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,21799,27903,27904,43600,43601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38465349$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pereira, Austin</creatorcontrib><creatorcontrib>Nichani, Prem A.H.</creatorcontrib><creatorcontrib>Yan, Peng</creatorcontrib><creatorcontrib>Micieli, Jonathan A.</creatorcontrib><title>Subfoveal Choroidal Neovascular Membrane Secondary to Idiopathic Intracranial Hypertension</title><title>Journal of vitreoretinal diseases (Print)</title><addtitle>J Vitreoretin Dis</addtitle><description>Purpose: To present a rare case of subfoveal choroidal neovascular membrane (CNVM) secondary to idiopathic intracranial hypertension. Methods: A case was evaluated. Results: A 21-year-old woman presented with a 2-week history of painless blurred vision in the right eye. She described initial metamorphopsia and intermittent bitemporal headaches lasting 30 minutes. She denied pain with eye movements and a history of trauma. Her body mass index was 49 kg/m2. The visual acuity (VA) was 20/320 OD and 20/20 OS; there was no relative afferent pupillary defect. A dilated fundus examination showed bilateral optic disc edema and a subfoveal CNVM in the right eye. The patient was started on oral acetazolamide 500 mg twice daily and treated with 2 intravitreal antivascular endothelial growth factor (anti-VEGF) injections. Three months later, the VA was 20/30 in the right eye and the disc edema had improved. Conclusions: CNVMs in the setting of idiopathic intracranial hypertension–related papilledema may be subfoveal and have an excellent response to anti-VEGF agents.</description><subject>Case Reports</subject><issn>2474-1264</issn><issn>2474-1272</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><recordid>eNp9UE1LAzEUDKLYUvsDvMj-ga353GRPIkVtoeqhevESstlsm7LdLMluof_elGpRBE9veG9m3jAAXCM4QYjzW0w5RTijmCCMBCP5GRgedinCHJ-fcEYHYBzCBkKIBSc4w5dgQATNGKH5EHws-6JyO6PqZLp23tkyohfjdirovlY-eTbbwqvGJEujXVMqv086l8xL61rVra1O5k3nlY4UG5WzfWt8Z5pgXXMFLipVBzP-miPw_vjwNp2li9en-fR-kWrCRJcyjrliCBfYCCQEEXmJWQYNKwoMS4U1FYLznFRZAStFK8SoQhGJTBPIkSYjcHf0bftia0ptDoFq2Xq7jWmlU1b-vjR2LVduJxHMMWW5iA7o6KC9C8Gb6iRGUB7Kln_Kjpqbn19Piu9qI2FyJAS1MnLjet_EFv5x_AQWPoig</recordid><startdate>20240301</startdate><enddate>20240301</enddate><creator>Pereira, Austin</creator><creator>Nichani, Prem A.H.</creator><creator>Yan, Peng</creator><creator>Micieli, Jonathan A.</creator><general>SAGE Publications</general><scope>AFRWT</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-3818-9788</orcidid></search><sort><creationdate>20240301</creationdate><title>Subfoveal Choroidal Neovascular Membrane Secondary to Idiopathic Intracranial Hypertension</title><author>Pereira, Austin ; Nichani, Prem A.H. ; Yan, Peng ; Micieli, Jonathan A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-5727a512b2e8188389d2560e5bb20da2c4887793f6b0fa4f154a10fa86c3071c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Case Reports</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pereira, Austin</creatorcontrib><creatorcontrib>Nichani, Prem A.H.</creatorcontrib><creatorcontrib>Yan, Peng</creatorcontrib><creatorcontrib>Micieli, Jonathan A.</creatorcontrib><collection>Sage Journals GOLD Open Access 2024</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of vitreoretinal diseases (Print)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pereira, Austin</au><au>Nichani, Prem A.H.</au><au>Yan, Peng</au><au>Micieli, Jonathan A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Subfoveal Choroidal Neovascular Membrane Secondary to Idiopathic Intracranial Hypertension</atitle><jtitle>Journal of vitreoretinal diseases (Print)</jtitle><addtitle>J Vitreoretin Dis</addtitle><date>2024-03-01</date><risdate>2024</risdate><volume>8</volume><issue>2</issue><spage>192</spage><epage>195</epage><pages>192-195</pages><issn>2474-1264</issn><eissn>2474-1272</eissn><abstract>Purpose: To present a rare case of subfoveal choroidal neovascular membrane (CNVM) secondary to idiopathic intracranial hypertension. Methods: A case was evaluated. Results: A 21-year-old woman presented with a 2-week history of painless blurred vision in the right eye. She described initial metamorphopsia and intermittent bitemporal headaches lasting 30 minutes. She denied pain with eye movements and a history of trauma. Her body mass index was 49 kg/m2. The visual acuity (VA) was 20/320 OD and 20/20 OS; there was no relative afferent pupillary defect. A dilated fundus examination showed bilateral optic disc edema and a subfoveal CNVM in the right eye. The patient was started on oral acetazolamide 500 mg twice daily and treated with 2 intravitreal antivascular endothelial growth factor (anti-VEGF) injections. Three months later, the VA was 20/30 in the right eye and the disc edema had improved. Conclusions: CNVMs in the setting of idiopathic intracranial hypertension–related papilledema may be subfoveal and have an excellent response to anti-VEGF agents.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>38465349</pmid><doi>10.1177/24741264231218539</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0003-3818-9788</orcidid><oa>free_for_read</oa></addata></record> |
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title | Subfoveal Choroidal Neovascular Membrane Secondary to Idiopathic Intracranial Hypertension |
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