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Hemolacria due to possible idiopathic intracranial hypertension: A case report
Background Hemolacria, the excretion of blood-tinged tears, merges biological oddity with mysticism. This report discusses a unique case of hemolacria in a patient with possible idiopathic intracranial hypertension without papilledema (IIHWOP), resolving after acetazolamide treatment, exploring a po...
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Published in: | Cephalalgia reports 2024-08, Vol.7 |
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creator | Braca, Simone Russo, Cinzia Valeria Stornaiuolo, Antonio Miele, Angelo Cretella, Gennaro Giannini, Caterina De Simone, Roberto |
description | Background
Hemolacria, the excretion of blood-tinged tears, merges biological oddity with mysticism. This report discusses a unique case of hemolacria in a patient with possible idiopathic intracranial hypertension without papilledema (IIHWOP), resolving after acetazolamide treatment, exploring a potential pathogenic link.
Case Presentation
A 50-year-old male experienced daily hemolacria for three months along with occasional epistaxis and otorrhagia. He also suffered from chronic migraine, often accompanied with blurred vision and vertigo, and primary stabbing headache. Systemic and neurological assessments, along with computed tomography (CT) brain scans, ophthalmological and hematological tests revealed no underlying diseases. Brain magnetic resonance imaging (MRI) along with magnetic resonance venography, indicated left transverse sinus aplasia, bilateral ocular bulb flattening and enlargement of optic nerve sheaths, suggesting increased intracranial pressure. The patient began acetazolamide treatment. In the next three months, he experienced only four bleeding episodes and a dramatic reduction of monthly migraine days.
Discussion
Our report first associates hemolacria with possible IIHWOP, proposing a new pathogenic pathway. A derangement in the glymphatic system, implicated in idiopathic intracranial hypertension pathophysiology, could explain its ocular symptoms, including hemolacria. Our findings may contribute to understanding IIHWOP and the glympathic system's role in ocular physiology. |
doi_str_mv | 10.1177/25158163241267322 |
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Hemolacria, the excretion of blood-tinged tears, merges biological oddity with mysticism. This report discusses a unique case of hemolacria in a patient with possible idiopathic intracranial hypertension without papilledema (IIHWOP), resolving after acetazolamide treatment, exploring a potential pathogenic link.
Case Presentation
A 50-year-old male experienced daily hemolacria for three months along with occasional epistaxis and otorrhagia. He also suffered from chronic migraine, often accompanied with blurred vision and vertigo, and primary stabbing headache. Systemic and neurological assessments, along with computed tomography (CT) brain scans, ophthalmological and hematological tests revealed no underlying diseases. Brain magnetic resonance imaging (MRI) along with magnetic resonance venography, indicated left transverse sinus aplasia, bilateral ocular bulb flattening and enlargement of optic nerve sheaths, suggesting increased intracranial pressure. The patient began acetazolamide treatment. In the next three months, he experienced only four bleeding episodes and a dramatic reduction of monthly migraine days.
Discussion
Our report first associates hemolacria with possible IIHWOP, proposing a new pathogenic pathway. A derangement in the glymphatic system, implicated in idiopathic intracranial hypertension pathophysiology, could explain its ocular symptoms, including hemolacria. Our findings may contribute to understanding IIHWOP and the glympathic system's role in ocular physiology.</description><identifier>ISSN: 2515-8163</identifier><identifier>EISSN: 2515-8163</identifier><identifier>DOI: 10.1177/25158163241267322</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Acetazolamide ; Aplasia ; Computed tomography ; Eye diseases ; Headache ; Hypertension ; Magnetic resonance imaging ; Migraine ; Neuroimaging ; Optic nerve ; Sheaths ; Swelling ; Tears</subject><ispartof>Cephalalgia reports, 2024-08, Vol.7</ispartof><rights>The Author(s) 2024</rights><rights>The Author(s) 2024. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2182-f34dd2aef8de37a2b22b427771234c379dabd03aeffa501ad9f3f1a3d825467e3</cites><orcidid>0000-0002-0954-8668</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/25158163241267322$$EPDF$$P50$$Gsage$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3149765129?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,21966,25753,27853,27924,27925,37012,44590,44945,45333</link.rule.ids></links><search><creatorcontrib>Braca, Simone</creatorcontrib><creatorcontrib>Russo, Cinzia Valeria</creatorcontrib><creatorcontrib>Stornaiuolo, Antonio</creatorcontrib><creatorcontrib>Miele, Angelo</creatorcontrib><creatorcontrib>Cretella, Gennaro</creatorcontrib><creatorcontrib>Giannini, Caterina</creatorcontrib><creatorcontrib>De Simone, Roberto</creatorcontrib><title>Hemolacria due to possible idiopathic intracranial hypertension: A case report</title><title>Cephalalgia reports</title><description>Background
Hemolacria, the excretion of blood-tinged tears, merges biological oddity with mysticism. This report discusses a unique case of hemolacria in a patient with possible idiopathic intracranial hypertension without papilledema (IIHWOP), resolving after acetazolamide treatment, exploring a potential pathogenic link.
Case Presentation
A 50-year-old male experienced daily hemolacria for three months along with occasional epistaxis and otorrhagia. He also suffered from chronic migraine, often accompanied with blurred vision and vertigo, and primary stabbing headache. Systemic and neurological assessments, along with computed tomography (CT) brain scans, ophthalmological and hematological tests revealed no underlying diseases. Brain magnetic resonance imaging (MRI) along with magnetic resonance venography, indicated left transverse sinus aplasia, bilateral ocular bulb flattening and enlargement of optic nerve sheaths, suggesting increased intracranial pressure. The patient began acetazolamide treatment. In the next three months, he experienced only four bleeding episodes and a dramatic reduction of monthly migraine days.
Discussion
Our report first associates hemolacria with possible IIHWOP, proposing a new pathogenic pathway. A derangement in the glymphatic system, implicated in idiopathic intracranial hypertension pathophysiology, could explain its ocular symptoms, including hemolacria. Our findings may contribute to understanding IIHWOP and the glympathic system's role in ocular physiology.</description><subject>Acetazolamide</subject><subject>Aplasia</subject><subject>Computed tomography</subject><subject>Eye diseases</subject><subject>Headache</subject><subject>Hypertension</subject><subject>Magnetic resonance imaging</subject><subject>Migraine</subject><subject>Neuroimaging</subject><subject>Optic nerve</subject><subject>Sheaths</subject><subject>Swelling</subject><subject>Tears</subject><issn>2515-8163</issn><issn>2515-8163</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1UU1LAzEUXETBUvsDvAU8tyYv2c2ut1LUFkQveg5v89GmbDdrsj3037u1ooJ4eo9hZt5jJsuuGZ0xJuUt5CwvWcFBMCgkBzjLRkdsegTPf-2X2SSlLaUUOBM5iFH2vLS70KCOHonZW9IH0oWUfN1Y4o0PHfYbr4lv-ziQsPXYkM2hs7G3bfKhvSNzojFZEm0XYn-VXThskp18zXH29nD_ulhOn14eV4v501QDK2HquDAG0LrSWC4RaoBagJSSAReay8pgbSgfCA5zytBUjjuG3JSQi0JaPs5WJ18TcKu66HcYDyqgV59AiGuFsfe6sYpCzQukeVlrLbgQlXOydnWhKdjKGDZ43Zy8uhje9zb1ahv2sR3eV0NKlSxyBtXAYieWjkM-0brvq4yqYwvqTwuDZnbSJFzbH9f_BR9u4Iac</recordid><startdate>202408</startdate><enddate>202408</enddate><creator>Braca, Simone</creator><creator>Russo, Cinzia Valeria</creator><creator>Stornaiuolo, Antonio</creator><creator>Miele, Angelo</creator><creator>Cretella, Gennaro</creator><creator>Giannini, Caterina</creator><creator>De Simone, Roberto</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><general>SAGE Publishing</general><scope>AFRWT</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-0954-8668</orcidid></search><sort><creationdate>202408</creationdate><title>Hemolacria due to possible idiopathic intracranial hypertension: A case report</title><author>Braca, Simone ; Russo, Cinzia Valeria ; Stornaiuolo, Antonio ; Miele, Angelo ; Cretella, Gennaro ; Giannini, Caterina ; De Simone, Roberto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2182-f34dd2aef8de37a2b22b427771234c379dabd03aeffa501ad9f3f1a3d825467e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Acetazolamide</topic><topic>Aplasia</topic><topic>Computed tomography</topic><topic>Eye diseases</topic><topic>Headache</topic><topic>Hypertension</topic><topic>Magnetic resonance imaging</topic><topic>Migraine</topic><topic>Neuroimaging</topic><topic>Optic nerve</topic><topic>Sheaths</topic><topic>Swelling</topic><topic>Tears</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Braca, Simone</creatorcontrib><creatorcontrib>Russo, Cinzia Valeria</creatorcontrib><creatorcontrib>Stornaiuolo, Antonio</creatorcontrib><creatorcontrib>Miele, Angelo</creatorcontrib><creatorcontrib>Cretella, Gennaro</creatorcontrib><creatorcontrib>Giannini, Caterina</creatorcontrib><creatorcontrib>De Simone, Roberto</creatorcontrib><collection>SAGE Open Access Journals</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Directory of Open Access Journals</collection><jtitle>Cephalalgia reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Braca, Simone</au><au>Russo, Cinzia Valeria</au><au>Stornaiuolo, Antonio</au><au>Miele, Angelo</au><au>Cretella, Gennaro</au><au>Giannini, Caterina</au><au>De Simone, Roberto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hemolacria due to possible idiopathic intracranial hypertension: A case report</atitle><jtitle>Cephalalgia reports</jtitle><date>2024-08</date><risdate>2024</risdate><volume>7</volume><issn>2515-8163</issn><eissn>2515-8163</eissn><abstract>Background
Hemolacria, the excretion of blood-tinged tears, merges biological oddity with mysticism. This report discusses a unique case of hemolacria in a patient with possible idiopathic intracranial hypertension without papilledema (IIHWOP), resolving after acetazolamide treatment, exploring a potential pathogenic link.
Case Presentation
A 50-year-old male experienced daily hemolacria for three months along with occasional epistaxis and otorrhagia. He also suffered from chronic migraine, often accompanied with blurred vision and vertigo, and primary stabbing headache. Systemic and neurological assessments, along with computed tomography (CT) brain scans, ophthalmological and hematological tests revealed no underlying diseases. Brain magnetic resonance imaging (MRI) along with magnetic resonance venography, indicated left transverse sinus aplasia, bilateral ocular bulb flattening and enlargement of optic nerve sheaths, suggesting increased intracranial pressure. The patient began acetazolamide treatment. In the next three months, he experienced only four bleeding episodes and a dramatic reduction of monthly migraine days.
Discussion
Our report first associates hemolacria with possible IIHWOP, proposing a new pathogenic pathway. A derangement in the glymphatic system, implicated in idiopathic intracranial hypertension pathophysiology, could explain its ocular symptoms, including hemolacria. Our findings may contribute to understanding IIHWOP and the glympathic system's role in ocular physiology.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><doi>10.1177/25158163241267322</doi><orcidid>https://orcid.org/0000-0002-0954-8668</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acetazolamide Aplasia Computed tomography Eye diseases Headache Hypertension Magnetic resonance imaging Migraine Neuroimaging Optic nerve Sheaths Swelling Tears |
title | Hemolacria due to possible idiopathic intracranial hypertension: A case report |
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