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Lhermitte-Duclos Disease Associated with Neurofibromatosis Type-1 and Non-Ossifying Fibroma
Lhermitte-Duclos disease (LDD) is a rare cerebellar disorder of uncertain pathogenesis characterized by enlargement of cerebellar folia. Magnetic resonance imaging is the diagnostic modality of choice and usually distinguishes the LDD by its characteristic "striated or laminated pattern" a...
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Published in: | Acta radiologica (1987) 2005-02, Vol.46 (1), p.97-100 |
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container_title | Acta radiologica (1987) |
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creator | Yesilda, A. Baykal, B. Ayata, A. Kerman, G. Koroglu, M. Olgar, S. Oyar, O. |
description | Lhermitte-Duclos disease (LDD) is a rare cerebellar disorder of uncertain pathogenesis characterized by enlargement of cerebellar folia. Magnetic resonance imaging is the diagnostic modality of choice and usually distinguishes the LDD by its characteristic "striated or laminated pattern" appearance. Various additional abnormalities have been reported in association with LDD. We report a case of LDD coexisting with neurofibromatosis type 1 (NF-1) and non-ossifying fibroma. |
doi_str_mv | 10.1080/02841850510020932 |
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Magnetic resonance imaging is the diagnostic modality of choice and usually distinguishes the LDD by its characteristic "striated or laminated pattern" appearance. Various additional abnormalities have been reported in association with LDD. We report a case of LDD coexisting with neurofibromatosis type 1 (NF-1) and non-ossifying fibroma.</description><identifier>ISSN: 0284-1851</identifier><identifier>EISSN: 1600-0455</identifier><identifier>DOI: 10.1080/02841850510020932</identifier><identifier>PMID: 15841746</identifier><identifier>CODEN: ACRAE3</identifier><language>eng</language><publisher>London, England: Informa UK Ltd</publisher><subject>Biological and medical sciences ; Bone Neoplasms - complications ; Bone Neoplasms - diagnosis ; Cerebellar Neoplasms - complications ; Cerebellar Neoplasms - diagnosis ; Child ; Fibroma - complications ; Fibroma - diagnosis ; Ganglioneuroma - complications ; Ganglioneuroma - diagnosis ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Neurofibromatosis 1 - complications ; Neurofibromatosis 1 - diagnosis ; Neurology ; Tibia ; Tumors of the nervous system. Phacomatoses</subject><ispartof>Acta radiologica (1987), 2005-02, Vol.46 (1), p.97-100</ispartof><rights>2005 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2005</rights><rights>2005 Taylor & Francis</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-a1a915c289a9256fee4542bf7c1eb6e48efa25e6420fa70963053a80fad4bd463</citedby><cites>FETCH-LOGICAL-c420t-a1a915c289a9256fee4542bf7c1eb6e48efa25e6420fa70963053a80fad4bd463</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925,79364</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16479980$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15841746$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yesilda, A.</creatorcontrib><creatorcontrib>Baykal, B.</creatorcontrib><creatorcontrib>Ayata, A.</creatorcontrib><creatorcontrib>Kerman, G.</creatorcontrib><creatorcontrib>Koroglu, M.</creatorcontrib><creatorcontrib>Olgar, S.</creatorcontrib><creatorcontrib>Oyar, O.</creatorcontrib><title>Lhermitte-Duclos Disease Associated with Neurofibromatosis Type-1 and Non-Ossifying Fibroma</title><title>Acta radiologica (1987)</title><addtitle>Acta Radiol</addtitle><description>Lhermitte-Duclos disease (LDD) is a rare cerebellar disorder of uncertain pathogenesis characterized by enlargement of cerebellar folia. Magnetic resonance imaging is the diagnostic modality of choice and usually distinguishes the LDD by its characteristic "striated or laminated pattern" appearance. Various additional abnormalities have been reported in association with LDD. We report a case of LDD coexisting with neurofibromatosis type 1 (NF-1) and non-ossifying fibroma.</description><subject>Biological and medical sciences</subject><subject>Bone Neoplasms - complications</subject><subject>Bone Neoplasms - diagnosis</subject><subject>Cerebellar Neoplasms - complications</subject><subject>Cerebellar Neoplasms - diagnosis</subject><subject>Child</subject><subject>Fibroma - complications</subject><subject>Fibroma - diagnosis</subject><subject>Ganglioneuroma - complications</subject><subject>Ganglioneuroma - diagnosis</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neurofibromatosis 1 - complications</subject><subject>Neurofibromatosis 1 - diagnosis</subject><subject>Neurology</subject><subject>Tibia</subject><subject>Tumors of the nervous system. Phacomatoses</subject><issn>0284-1851</issn><issn>1600-0455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqN0MFq3DAQBmBRWppt2gfopfjS3pyOZEm26SkkTVpYkkt66sGM5VFWwba2Gpuwb18HL-RQCD2JQd8_A78QHyWcSajgK6hKy8qAkQAK6kK9EhtpAXLQxrwWm6f_fAHyRLxjfgCQqjTyrTiRZgmW2m7E7-2O0hCmifLL2fWRs8vAhEzZOXN0ASfqsscw7bIbmlP0oU1xwCly4OzusKdcZjh22U0c81vm4A9hvM-uVvVevPHYM304vqfi19X3u4sf-fb2-ufF-TZ3WsGUo8RaGqeqGmtlrCfSRqvWl05Sa0lX5FEZsgv2WEJtCzAFVsvQ6bbTtjgVX9a9-xT_zMRTMwR21Pc4Upy5sWVpi0rWC5QrdCkyJ_LNPoUB06GR0Dw12vzT6JL5dFw-twN1z4ljhQv4fATIDnufcHSBn53VZV1XsLiz1THeU_MQ5zQupbx4-dsaCKOPacAdYT_tHKb_Sv8FrfedRA</recordid><startdate>20050201</startdate><enddate>20050201</enddate><creator>Yesilda, A.</creator><creator>Baykal, B.</creator><creator>Ayata, A.</creator><creator>Kerman, G.</creator><creator>Koroglu, M.</creator><creator>Olgar, S.</creator><creator>Oyar, O.</creator><general>Informa UK Ltd</general><general>SAGE Publications</general><general>Taylor & Francis</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>20050201</creationdate><title>Lhermitte-Duclos Disease Associated with Neurofibromatosis Type-1 and Non-Ossifying Fibroma</title><author>Yesilda, A. ; Baykal, B. ; Ayata, A. ; Kerman, G. ; Koroglu, M. ; Olgar, S. ; Oyar, O.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-a1a915c289a9256fee4542bf7c1eb6e48efa25e6420fa70963053a80fad4bd463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Biological and medical sciences</topic><topic>Bone Neoplasms - complications</topic><topic>Bone Neoplasms - diagnosis</topic><topic>Cerebellar Neoplasms - complications</topic><topic>Cerebellar Neoplasms - diagnosis</topic><topic>Child</topic><topic>Fibroma - complications</topic><topic>Fibroma - diagnosis</topic><topic>Ganglioneuroma - complications</topic><topic>Ganglioneuroma - diagnosis</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neurofibromatosis 1 - complications</topic><topic>Neurofibromatosis 1 - diagnosis</topic><topic>Neurology</topic><topic>Tibia</topic><topic>Tumors of the nervous system. Phacomatoses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yesilda, A.</creatorcontrib><creatorcontrib>Baykal, B.</creatorcontrib><creatorcontrib>Ayata, A.</creatorcontrib><creatorcontrib>Kerman, G.</creatorcontrib><creatorcontrib>Koroglu, M.</creatorcontrib><creatorcontrib>Olgar, S.</creatorcontrib><creatorcontrib>Oyar, O.</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>Acta radiologica (1987)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yesilda, A.</au><au>Baykal, B.</au><au>Ayata, A.</au><au>Kerman, G.</au><au>Koroglu, M.</au><au>Olgar, S.</au><au>Oyar, O.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lhermitte-Duclos Disease Associated with Neurofibromatosis Type-1 and Non-Ossifying Fibroma</atitle><jtitle>Acta radiologica (1987)</jtitle><addtitle>Acta Radiol</addtitle><date>2005-02-01</date><risdate>2005</risdate><volume>46</volume><issue>1</issue><spage>97</spage><epage>100</epage><pages>97-100</pages><issn>0284-1851</issn><eissn>1600-0455</eissn><coden>ACRAE3</coden><abstract>Lhermitte-Duclos disease (LDD) is a rare cerebellar disorder of uncertain pathogenesis characterized by enlargement of cerebellar folia. Magnetic resonance imaging is the diagnostic modality of choice and usually distinguishes the LDD by its characteristic "striated or laminated pattern" appearance. Various additional abnormalities have been reported in association with LDD. We report a case of LDD coexisting with neurofibromatosis type 1 (NF-1) and non-ossifying fibroma.</abstract><cop>London, England</cop><pub>Informa UK Ltd</pub><pmid>15841746</pmid><doi>10.1080/02841850510020932</doi><tpages>4</tpages></addata></record> |
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subjects | Biological and medical sciences Bone Neoplasms - complications Bone Neoplasms - diagnosis Cerebellar Neoplasms - complications Cerebellar Neoplasms - diagnosis Child Fibroma - complications Fibroma - diagnosis Ganglioneuroma - complications Ganglioneuroma - diagnosis Humans Investigative techniques, diagnostic techniques (general aspects) Male Medical sciences Neurofibromatosis 1 - complications Neurofibromatosis 1 - diagnosis Neurology Tibia Tumors of the nervous system. Phacomatoses |
title | Lhermitte-Duclos Disease Associated with Neurofibromatosis Type-1 and Non-Ossifying Fibroma |
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