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Cavernous angioma presenting as epilepsy 13 years after initial diagnosis
A 22-year-old man presented with tonic-clonic seizure and was admitted to our hospital. He had suffered from frequent headaches, and had been diagnosed with a brain tumour on MRI 13 years ago. However, neither further examination nor follow-up neuroimaging study have been performed. Computed tomogra...
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Published in: | Journal of clinical neuroscience 2004-05, Vol.11 (4), p.430-432 |
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cites | cdi_FETCH-LOGICAL-c352t-22c9d5eb27893cc1d3f23c8a2c3e5e3d2a51f4f1ba1ba105a8417fa85f5c7d673 |
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creator | Murakami, Kensuke Umezawa, Kunihiko Kaimori, Mitsuomi Nishijima, Michiharu |
description | A 22-year-old man presented with tonic-clonic seizure and was admitted to our hospital. He had suffered from frequent headaches, and had been diagnosed with a brain tumour on MRI 13 years ago. However, neither further examination nor follow-up neuroimaging study have been performed. Computed tomography and magnetic resonance imaging demonstrated an intraaxial tumor with granular calcification in the right frontal lobe, attached to the adjacent dura mater, which was enlarged compared with the lesion on CT 13 years before. The lesion was surgically excised through right frontal craniotomy. Histopathological analysis indicated cavernous angioma.
In cavernous angioma in younger children, more aggressive surgical indications than in adults may be favorable both to prevent haemorrhagic complications and to confirm pathologic diagnosis. |
doi_str_mv | 10.1016/j.jocn.2003.05.010 |
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In cavernous angioma in younger children, more aggressive surgical indications than in adults may be favorable both to prevent haemorrhagic complications and to confirm pathologic diagnosis.</description><identifier>ISSN: 0967-5868</identifier><identifier>EISSN: 1532-2653</identifier><identifier>DOI: 10.1016/j.jocn.2003.05.010</identifier><identifier>PMID: 15080966</identifier><language>eng</language><publisher>Scotland: Elsevier Ltd</publisher><subject>Adult ; Brain Neoplasms - diagnosis ; Brain Neoplasms - surgery ; Cavernous angioma ; Epilepsy ; Epilepsy - etiology ; Hemangioma, Cavernous - diagnosis ; Humans ; Magnetic Resonance Imaging - methods ; Male ; Surgery ; Tomography, X-Ray Computed - methods</subject><ispartof>Journal of clinical neuroscience, 2004-05, Vol.11 (4), p.430-432</ispartof><rights>2004 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-22c9d5eb27893cc1d3f23c8a2c3e5e3d2a51f4f1ba1ba105a8417fa85f5c7d673</citedby><cites>FETCH-LOGICAL-c352t-22c9d5eb27893cc1d3f23c8a2c3e5e3d2a51f4f1ba1ba105a8417fa85f5c7d673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15080966$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Murakami, Kensuke</creatorcontrib><creatorcontrib>Umezawa, Kunihiko</creatorcontrib><creatorcontrib>Kaimori, Mitsuomi</creatorcontrib><creatorcontrib>Nishijima, Michiharu</creatorcontrib><title>Cavernous angioma presenting as epilepsy 13 years after initial diagnosis</title><title>Journal of clinical neuroscience</title><addtitle>J Clin Neurosci</addtitle><description>A 22-year-old man presented with tonic-clonic seizure and was admitted to our hospital. He had suffered from frequent headaches, and had been diagnosed with a brain tumour on MRI 13 years ago. However, neither further examination nor follow-up neuroimaging study have been performed. Computed tomography and magnetic resonance imaging demonstrated an intraaxial tumor with granular calcification in the right frontal lobe, attached to the adjacent dura mater, which was enlarged compared with the lesion on CT 13 years before. The lesion was surgically excised through right frontal craniotomy. Histopathological analysis indicated cavernous angioma.
In cavernous angioma in younger children, more aggressive surgical indications than in adults may be favorable both to prevent haemorrhagic complications and to confirm pathologic diagnosis.</description><subject>Adult</subject><subject>Brain Neoplasms - diagnosis</subject><subject>Brain Neoplasms - surgery</subject><subject>Cavernous angioma</subject><subject>Epilepsy</subject><subject>Epilepsy - etiology</subject><subject>Hemangioma, Cavernous - diagnosis</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Surgery</subject><subject>Tomography, X-Ray Computed - methods</subject><issn>0967-5868</issn><issn>1532-2653</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEQhoMotlb_gAfZk7ddJ0mzH-BFih-Fghc9hzSZlCy72TXZFvrv3aUFb8LAHOZ5X5iHkHsKGQWaP9VZ3WmfMQCegciAwgWZU8FZynLBL8kcqrxIRZmXM3ITYw0A1ZLDNZlRAeV4zOdkvVIHDL7bx0T5netalfQBI_rB-V2iYoK9a7CPx4Ty5IgqjJwdMCTOu8GpJjFO7XwXXbwlV1Y1Ee_Oe0G-316_Vh_p5vN9vXrZpJoLNqSM6coI3LKirLjW1HDLuC4V0xwFcsOUoHZp6VZNA0KVS1pYVQordGHygi_I46m3D93PHuMgWxc1No3yOL4hC1oy4IyPIDuBOnQxBrSyD65V4SgpyEmgrOUkUE4CJQg5ChxDD-f2_bZF8xc5GxuB5xOA448Hh0FG7dBrNC6gHqTp3H_9v-68giE</recordid><startdate>20040501</startdate><enddate>20040501</enddate><creator>Murakami, Kensuke</creator><creator>Umezawa, Kunihiko</creator><creator>Kaimori, Mitsuomi</creator><creator>Nishijima, Michiharu</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20040501</creationdate><title>Cavernous angioma presenting as epilepsy 13 years after initial diagnosis</title><author>Murakami, Kensuke ; Umezawa, Kunihiko ; Kaimori, Mitsuomi ; Nishijima, Michiharu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-22c9d5eb27893cc1d3f23c8a2c3e5e3d2a51f4f1ba1ba105a8417fa85f5c7d673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Brain Neoplasms - diagnosis</topic><topic>Brain Neoplasms - surgery</topic><topic>Cavernous angioma</topic><topic>Epilepsy</topic><topic>Epilepsy - etiology</topic><topic>Hemangioma, Cavernous - diagnosis</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Surgery</topic><topic>Tomography, X-Ray Computed - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Murakami, Kensuke</creatorcontrib><creatorcontrib>Umezawa, Kunihiko</creatorcontrib><creatorcontrib>Kaimori, Mitsuomi</creatorcontrib><creatorcontrib>Nishijima, Michiharu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Murakami, Kensuke</au><au>Umezawa, Kunihiko</au><au>Kaimori, Mitsuomi</au><au>Nishijima, Michiharu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cavernous angioma presenting as epilepsy 13 years after initial diagnosis</atitle><jtitle>Journal of clinical neuroscience</jtitle><addtitle>J Clin Neurosci</addtitle><date>2004-05-01</date><risdate>2004</risdate><volume>11</volume><issue>4</issue><spage>430</spage><epage>432</epage><pages>430-432</pages><issn>0967-5868</issn><eissn>1532-2653</eissn><abstract>A 22-year-old man presented with tonic-clonic seizure and was admitted to our hospital. He had suffered from frequent headaches, and had been diagnosed with a brain tumour on MRI 13 years ago. However, neither further examination nor follow-up neuroimaging study have been performed. Computed tomography and magnetic resonance imaging demonstrated an intraaxial tumor with granular calcification in the right frontal lobe, attached to the adjacent dura mater, which was enlarged compared with the lesion on CT 13 years before. The lesion was surgically excised through right frontal craniotomy. Histopathological analysis indicated cavernous angioma.
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subjects | Adult Brain Neoplasms - diagnosis Brain Neoplasms - surgery Cavernous angioma Epilepsy Epilepsy - etiology Hemangioma, Cavernous - diagnosis Humans Magnetic Resonance Imaging - methods Male Surgery Tomography, X-Ray Computed - methods |
title | Cavernous angioma presenting as epilepsy 13 years after initial diagnosis |
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