A case of meningioangiomatosis without von Recklinghausen's disease: report of a case and review of 13 cases
Meningioangiomatosis is rare disease and is classified as hamartoma in central neurofibromatosis. Unlike most cases of meningioangiomatosis, the very rare case reported here was not associated with von Recklinghausen's disease. We could find only 12 previous cases reported in the literature. A...
Gespeichert in:
| Veröffentlicht in: | Child's nervous system 1994-03, Vol.10 (2), p.126-130 |
|---|---|
| Hauptverfasser: | , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 130 |
|---|---|
| container_issue | 2 |
| container_start_page | 126 |
| container_title | Child's nervous system |
| container_volume | 10 |
| creator | HARADA, K INAGAWA, T NAGASAKO, R |
| description | Meningioangiomatosis is rare disease and is classified as hamartoma in central neurofibromatosis. Unlike most cases of meningioangiomatosis, the very rare case reported here was not associated with von Recklinghausen's disease. We could find only 12 previous cases reported in the literature. A review was carried out of the clinical features, imaging characteristics, and histopathological findings in those 12 plus ours for a total 13 cases. Several types of convulsion were identified as clinical symptoms in 11 of the 13 cases. They were treated surgically. Prognosis was satisfactory in most cases. Proliferation of small blood vessels accompanied by endothelial cells with glial tissue as background and proliferation of fibroblasts or meningothelial cells in the perivascular space were observed to be the most frequent histopathological features. |
| doi_str_mv | 10.1007/BF00302777 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_76605284</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>76605284</sourcerecordid><originalsourceid>FETCH-LOGICAL-c270t-d53bcc52056ceb58931ee42cf0ee8bc21cf0ec4c5d0246c8881b316393fc346f3</originalsourceid><addsrcrecordid>eNpFkE1LxDAQhoMouq5evAs9iIJQnXy1XW-r-AULgui5pOlUo22zdtpd_Pe2btFLEt558sC8jB1xuOAA8eX1HYAEEcfxFptwJWUIUsM2m4DQURiDgj22T_QBwHUiZrtsNwEpecQnrJwH1hAGvggqrF395rwZjsq0nhwFa9e--64NVr4OntF-lj3ybjrC-oyC3BH2n6-CBpe-aQeJ2ehMnffhyuF6CLn8TemA7RSmJDwc7yl7vbt9uXkIF0_3jzfzRWhFDG2Ya5lZqwXoyGKmk5nkiErYAhCTzAo-vKyyOgehIpskCc_6beRMFlaqqJBTdrrxLhv_1SG1aeXIYlmaGn1HaRxFoEWievB8A9rGEzVYpMvGVab5TjmkQ7Xpf7U9fDxau6zC_A8du-znJ-PckDVl0ZjaOvrDVK9TcSR_AKCtgA0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>76605284</pqid></control><display><type>article</type><title>A case of meningioangiomatosis without von Recklinghausen's disease: report of a case and review of 13 cases</title><source>MEDLINE</source><source>SpringerNature Journals</source><creator>HARADA, K ; INAGAWA, T ; NAGASAKO, R</creator><creatorcontrib>HARADA, K ; INAGAWA, T ; NAGASAKO, R</creatorcontrib><description>Meningioangiomatosis is rare disease and is classified as hamartoma in central neurofibromatosis. Unlike most cases of meningioangiomatosis, the very rare case reported here was not associated with von Recklinghausen's disease. We could find only 12 previous cases reported in the literature. A review was carried out of the clinical features, imaging characteristics, and histopathological findings in those 12 plus ours for a total 13 cases. Several types of convulsion were identified as clinical symptoms in 11 of the 13 cases. They were treated surgically. Prognosis was satisfactory in most cases. Proliferation of small blood vessels accompanied by endothelial cells with glial tissue as background and proliferation of fibroblasts or meningothelial cells in the perivascular space were observed to be the most frequent histopathological features.</description><identifier>ISSN: 0256-7040</identifier><identifier>EISSN: 1433-0350</identifier><identifier>DOI: 10.1007/BF00302777</identifier><identifier>PMID: 8033161</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Adolescent ; Biological and medical sciences ; Biomarkers, Tumor - analysis ; Craniotomy ; Frontal Lobe - pathology ; Frontal Lobe - surgery ; Humans ; Male ; Medical sciences ; Meningioma - diagnosis ; Meningioma - pathology ; Meningioma - surgery ; Neurofibromatosis 1 - diagnosis ; Neurofibromatosis 1 - pathology ; Neurofibromatosis 1 - surgery ; Neuroglia - pathology ; Neurologic Examination ; Neurology ; Neurons - pathology ; Phosphopyruvate Hydratase - analysis ; S100 Proteins - analysis ; Tumors of the nervous system. Phacomatoses</subject><ispartof>Child's nervous system, 1994-03, Vol.10 (2), p.126-130</ispartof><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c270t-d53bcc52056ceb58931ee42cf0ee8bc21cf0ec4c5d0246c8881b316393fc346f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4007476$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8033161$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HARADA, K</creatorcontrib><creatorcontrib>INAGAWA, T</creatorcontrib><creatorcontrib>NAGASAKO, R</creatorcontrib><title>A case of meningioangiomatosis without von Recklinghausen's disease: report of a case and review of 13 cases</title><title>Child's nervous system</title><addtitle>Childs Nerv Syst</addtitle><description>Meningioangiomatosis is rare disease and is classified as hamartoma in central neurofibromatosis. Unlike most cases of meningioangiomatosis, the very rare case reported here was not associated with von Recklinghausen's disease. We could find only 12 previous cases reported in the literature. A review was carried out of the clinical features, imaging characteristics, and histopathological findings in those 12 plus ours for a total 13 cases. Several types of convulsion were identified as clinical symptoms in 11 of the 13 cases. They were treated surgically. Prognosis was satisfactory in most cases. Proliferation of small blood vessels accompanied by endothelial cells with glial tissue as background and proliferation of fibroblasts or meningothelial cells in the perivascular space were observed to be the most frequent histopathological features.</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Craniotomy</subject><subject>Frontal Lobe - pathology</subject><subject>Frontal Lobe - surgery</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Meningioma - diagnosis</subject><subject>Meningioma - pathology</subject><subject>Meningioma - surgery</subject><subject>Neurofibromatosis 1 - diagnosis</subject><subject>Neurofibromatosis 1 - pathology</subject><subject>Neurofibromatosis 1 - surgery</subject><subject>Neuroglia - pathology</subject><subject>Neurologic Examination</subject><subject>Neurology</subject><subject>Neurons - pathology</subject><subject>Phosphopyruvate Hydratase - analysis</subject><subject>S100 Proteins - analysis</subject><subject>Tumors of the nervous system. Phacomatoses</subject><issn>0256-7040</issn><issn>1433-0350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1LxDAQhoMouq5evAs9iIJQnXy1XW-r-AULgui5pOlUo22zdtpd_Pe2btFLEt558sC8jB1xuOAA8eX1HYAEEcfxFptwJWUIUsM2m4DQURiDgj22T_QBwHUiZrtsNwEpecQnrJwH1hAGvggqrF395rwZjsq0nhwFa9e--64NVr4OntF-lj3ybjrC-oyC3BH2n6-CBpe-aQeJ2ehMnffhyuF6CLn8TemA7RSmJDwc7yl7vbt9uXkIF0_3jzfzRWhFDG2Ya5lZqwXoyGKmk5nkiErYAhCTzAo-vKyyOgehIpskCc_6beRMFlaqqJBTdrrxLhv_1SG1aeXIYlmaGn1HaRxFoEWievB8A9rGEzVYpMvGVab5TjmkQ7Xpf7U9fDxau6zC_A8du-znJ-PckDVl0ZjaOvrDVK9TcSR_AKCtgA0</recordid><startdate>19940301</startdate><enddate>19940301</enddate><creator>HARADA, K</creator><creator>INAGAWA, T</creator><creator>NAGASAKO, R</creator><general>Springer</general><scope>IQODW</scope><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>19940301</creationdate><title>A case of meningioangiomatosis without von Recklinghausen's disease: report of a case and review of 13 cases</title><author>HARADA, K ; INAGAWA, T ; NAGASAKO, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c270t-d53bcc52056ceb58931ee42cf0ee8bc21cf0ec4c5d0246c8881b316393fc346f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Craniotomy</topic><topic>Frontal Lobe - pathology</topic><topic>Frontal Lobe - surgery</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Meningioma - diagnosis</topic><topic>Meningioma - pathology</topic><topic>Meningioma - surgery</topic><topic>Neurofibromatosis 1 - diagnosis</topic><topic>Neurofibromatosis 1 - pathology</topic><topic>Neurofibromatosis 1 - surgery</topic><topic>Neuroglia - pathology</topic><topic>Neurologic Examination</topic><topic>Neurology</topic><topic>Neurons - pathology</topic><topic>Phosphopyruvate Hydratase - analysis</topic><topic>S100 Proteins - analysis</topic><topic>Tumors of the nervous system. Phacomatoses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HARADA, K</creatorcontrib><creatorcontrib>INAGAWA, T</creatorcontrib><creatorcontrib>NAGASAKO, R</creatorcontrib><collection>Pascal-Francis</collection><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>Child's nervous system</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HARADA, K</au><au>INAGAWA, T</au><au>NAGASAKO, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A case of meningioangiomatosis without von Recklinghausen's disease: report of a case and review of 13 cases</atitle><jtitle>Child's nervous system</jtitle><addtitle>Childs Nerv Syst</addtitle><date>1994-03-01</date><risdate>1994</risdate><volume>10</volume><issue>2</issue><spage>126</spage><epage>130</epage><pages>126-130</pages><issn>0256-7040</issn><eissn>1433-0350</eissn><abstract>Meningioangiomatosis is rare disease and is classified as hamartoma in central neurofibromatosis. Unlike most cases of meningioangiomatosis, the very rare case reported here was not associated with von Recklinghausen's disease. We could find only 12 previous cases reported in the literature. A review was carried out of the clinical features, imaging characteristics, and histopathological findings in those 12 plus ours for a total 13 cases. Several types of convulsion were identified as clinical symptoms in 11 of the 13 cases. They were treated surgically. Prognosis was satisfactory in most cases. Proliferation of small blood vessels accompanied by endothelial cells with glial tissue as background and proliferation of fibroblasts or meningothelial cells in the perivascular space were observed to be the most frequent histopathological features.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>8033161</pmid><doi>10.1007/BF00302777</doi><tpages>5</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0256-7040 |
| ispartof | Child's nervous system, 1994-03, Vol.10 (2), p.126-130 |
| issn | 0256-7040 1433-0350 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_76605284 |
| source | MEDLINE; SpringerNature Journals |
| subjects | Adolescent Biological and medical sciences Biomarkers, Tumor - analysis Craniotomy Frontal Lobe - pathology Frontal Lobe - surgery Humans Male Medical sciences Meningioma - diagnosis Meningioma - pathology Meningioma - surgery Neurofibromatosis 1 - diagnosis Neurofibromatosis 1 - pathology Neurofibromatosis 1 - surgery Neuroglia - pathology Neurologic Examination Neurology Neurons - pathology Phosphopyruvate Hydratase - analysis S100 Proteins - analysis Tumors of the nervous system. Phacomatoses |
| title | A case of meningioangiomatosis without von Recklinghausen's disease: report of a case and review of 13 cases |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T17%3A22%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20case%20of%20meningioangiomatosis%20without%20von%20Recklinghausen's%20disease:%20report%20of%20a%20case%20and%20review%20of%2013%20cases&rft.jtitle=Child's%20nervous%20system&rft.au=HARADA,%20K&rft.date=1994-03-01&rft.volume=10&rft.issue=2&rft.spage=126&rft.epage=130&rft.pages=126-130&rft.issn=0256-7040&rft.eissn=1433-0350&rft_id=info:doi/10.1007/BF00302777&rft_dat=%3Cproquest_cross%3E76605284%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=76605284&rft_id=info:pmid/8033161&rfr_iscdi=true |