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Jeudi : 8h-18h30
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Attention,
Votre centre de documentation sera fermé ce lundi 26 août.
Également, ce mercredi 28 août il sera fermé de 12 à 13h.
Enfin, ce jeudi 29 août il ouvrira à 14h45.
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Exostoses, enchondromatosis and metachondromatosis; diagnosis and management / John McFarlane in Acta Orthopaedica Belgica, Vol.82/1 (March 2016)
[article]
Titre : Exostoses, enchondromatosis and metachondromatosis; diagnosis and management Type de document : texte imprimé Auteurs : John McFarlane ; Tim Knight ; Anubha Sinha ; [et al...] Année de publication : 2016 Article en page(s) : p. 102-105 Langues : Anglais (eng) Mots-clés : dysplasie osseuse enchondrome métachondromatose malformation osseuse Résumé : We describe a 5 years old girl who presented to the multidisciplinary skeletal dysplasia clinic following excision of two bony lumps from her fingers. Based on clinical examination, radiolographs and histological results an initial diagnosis of hereditary multiple exostosis (HME) was made. Four years later she developed further lumps which had the radiological appearance of enchondromas. The appearance of both exostoses and enchondromas suggested a possible diagnosis of metachondromatosis. Genetic testing revealed a splice site mutation at the end of exon 11 on the PTPN11 gene, confirming the diagnosis of metachondromatosis. While both single or multiple exostoses and enchondromas occur relatively commonly on their own, the appearance of multiple exostoses and enchondromas together is rare and should raise the differential diagnosis of metachondromatosis. Making this diagnosis is important as the lesions in metachondromatosis may spontaneously resolve and therefore surgical intervention is often unnecessary. We discuss the diagnostic findings, genetic causes, treatment and prognosis of this rare condition of which less than thirty cases have previously been reported. Permalink : ./index.php?lvl=notice_display&id=46051
in Acta Orthopaedica Belgica > Vol.82/1 (March 2016) . - p. 102-105[article] Exostoses, enchondromatosis and metachondromatosis; diagnosis and management [texte imprimé] / John McFarlane ; Tim Knight ; Anubha Sinha ; [et al...] . - 2016 . - p. 102-105.
Langues : Anglais (eng)
in Acta Orthopaedica Belgica > Vol.82/1 (March 2016) . - p. 102-105
Mots-clés : dysplasie osseuse enchondrome métachondromatose malformation osseuse Résumé : We describe a 5 years old girl who presented to the multidisciplinary skeletal dysplasia clinic following excision of two bony lumps from her fingers. Based on clinical examination, radiolographs and histological results an initial diagnosis of hereditary multiple exostosis (HME) was made. Four years later she developed further lumps which had the radiological appearance of enchondromas. The appearance of both exostoses and enchondromas suggested a possible diagnosis of metachondromatosis. Genetic testing revealed a splice site mutation at the end of exon 11 on the PTPN11 gene, confirming the diagnosis of metachondromatosis. While both single or multiple exostoses and enchondromas occur relatively commonly on their own, the appearance of multiple exostoses and enchondromas together is rare and should raise the differential diagnosis of metachondromatosis. Making this diagnosis is important as the lesions in metachondromatosis may spontaneously resolve and therefore surgical intervention is often unnecessary. We discuss the diagnostic findings, genetic causes, treatment and prognosis of this rare condition of which less than thirty cases have previously been reported. Permalink : ./index.php?lvl=notice_display&id=46051 Exemplaires (1)
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