Association of Lhermitte–Duclos disease and split cord malformation in a child
Abstract Lhermitte–Duclos disease (LDD) or cerebellar gangliocytoma is a rare pathological entity, the etiology of which remains controversial. Numerous developmental anomalies are known to be associated with LDD, but the association between LDD and split cord malformation (SCM) has not been reporte...
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| Veröffentlicht in: | Journal of clinical neuroscience 2014-11, Vol.21 (11), p.1999-2002 |
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| container_end_page | 2002 |
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| container_issue | 11 |
| container_start_page | 1999 |
| container_title | Journal of clinical neuroscience |
| container_volume | 21 |
| creator | Abi Lahoud, Georges Chalouhi, Nohra Zanaty, Mario Rizk, Tony Jabbour, Pascal |
| description | Abstract Lhermitte–Duclos disease (LDD) or cerebellar gangliocytoma is a rare pathological entity, the etiology of which remains controversial. Numerous developmental anomalies are known to be associated with LDD, but the association between LDD and split cord malformation (SCM) has not been reported to our knowledge. We report LDD in a 3-year-old girl in whom repetitive urinary tract infections led to the diagnosis of a neurogenic bladder. Thorough screening revealed a SCM at the thoracic level which was surgically repaired. The pathogenesis of this entity and management strategies are discussed in this paper. |
| doi_str_mv | 10.1016/j.jocn.2014.05.005 |
| format | Article |
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Numerous developmental anomalies are known to be associated with LDD, but the association between LDD and split cord malformation (SCM) has not been reported to our knowledge. We report LDD in a 3-year-old girl in whom repetitive urinary tract infections led to the diagnosis of a neurogenic bladder. Thorough screening revealed a SCM at the thoracic level which was surgically repaired. 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Numerous developmental anomalies are known to be associated with LDD, but the association between LDD and split cord malformation (SCM) has not been reported to our knowledge. We report LDD in a 3-year-old girl in whom repetitive urinary tract infections led to the diagnosis of a neurogenic bladder. Thorough screening revealed a SCM at the thoracic level which was surgically repaired. The pathogenesis of this entity and management strategies are discussed in this paper.</description><subject>Cerebellar Neoplasms - diagnosis</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cowden syndrome</subject><subject>Diagnosis, Differential</subject><subject>Dysplastic cerebellar gangliocytoma</subject><subject>Female</subject><subject>Ganglioneuroma - diagnosis</subject><subject>Hamartoma Syndrome, Multiple - complications</subject><subject>Hamartoma Syndrome, Multiple - diagnosis</subject><subject>Hamartoma Syndrome, Multiple - pathology</subject><subject>Hamartoma Syndrome, Multiple - surgery</subject><subject>Humans</subject><subject>Lhermitte–Duclos disease</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Neurology</subject><subject>Neurosurgical Procedures</subject><subject>Spinal Cord - abnormalities</subject><subject>Spinal Cord - surgery</subject><subject>Split cord malformation</subject><subject>Thoracic Vertebrae</subject><subject>Treatment Outcome</subject><subject>Urinary Bladder, Neurogenic - etiology</subject><subject>Urinary Tract Infections - etiology</subject><subject>Urinary Tract Infections - microbiology</subject><issn>0967-5868</issn><issn>1532-2653</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc2K1UAQhRtRnDujL-BCsnSTWP2Tvt0gwjA6KlxQUNdNp1JhOibpa3cizM538A19EhPu6MKFuKpFfecsvsPYEw4VB66f91UfcaoEcFVBXQHU99iO11KUQtfyPtuB1fuyNtqcsfOcewCwSsJDdiaUlUYatWMfLnOOGPwc4lTErjjcUBrDPNPP7z9eLTjEXLQhk89U-Kkt8nEIc4ExtcXohy6m8ZQMU-ELvAlD-4g96PyQ6fHdvWCfr19_unpbHt6_eXd1eShRCTOXCISkNRkFCHLPFbTS7y0HC2QlqdqYfSOaRvvONusXVWdsRy0ZpE6glhfs2an3mOLXhfLsxpCRhsFPFJfsuJY1CC6M-Q9UWKs1N3xFxQnFFHNO1LljCqNPt46D26S73m3S3SbdQe1W6Wvo6V3_0ozU_on8trwCL04ArUK-BUouY6AJqQ2JcHZtDP_uf_lXHIcwBfTDF7ql3MclTatqx10WDtzHbfZt9VUbCA1K_gJMhahs</recordid><startdate>20141101</startdate><enddate>20141101</enddate><creator>Abi Lahoud, Georges</creator><creator>Chalouhi, Nohra</creator><creator>Zanaty, Mario</creator><creator>Rizk, Tony</creator><creator>Jabbour, Pascal</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><scope>7TK</scope></search><sort><creationdate>20141101</creationdate><title>Association of Lhermitte–Duclos disease and split cord malformation in a child</title><author>Abi Lahoud, Georges ; 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Numerous developmental anomalies are known to be associated with LDD, but the association between LDD and split cord malformation (SCM) has not been reported to our knowledge. We report LDD in a 3-year-old girl in whom repetitive urinary tract infections led to the diagnosis of a neurogenic bladder. Thorough screening revealed a SCM at the thoracic level which was surgically repaired. The pathogenesis of this entity and management strategies are discussed in this paper.</abstract><cop>Scotland</cop><pub>Elsevier Ltd</pub><pmid>24938384</pmid><doi>10.1016/j.jocn.2014.05.005</doi><tpages>4</tpages></addata></record> |
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| subjects | Cerebellar Neoplasms - diagnosis Child Child, Preschool Cowden syndrome Diagnosis, Differential Dysplastic cerebellar gangliocytoma Female Ganglioneuroma - diagnosis Hamartoma Syndrome, Multiple - complications Hamartoma Syndrome, Multiple - diagnosis Hamartoma Syndrome, Multiple - pathology Hamartoma Syndrome, Multiple - surgery Humans Lhermitte–Duclos disease Magnetic Resonance Imaging - methods Neurology Neurosurgical Procedures Spinal Cord - abnormalities Spinal Cord - surgery Split cord malformation Thoracic Vertebrae Treatment Outcome Urinary Bladder, Neurogenic - etiology Urinary Tract Infections - etiology Urinary Tract Infections - microbiology |
| title | Association of Lhermitte–Duclos disease and split cord malformation in a child |
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