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Growing skull hemangioma: first and unique description in a patient with Klippel-Trénaunay-Weber syndrome.
van der Loo, Lars E; Beckervordersandforth, Jan; Colon, Albert J; Schijns, Olaf E M G.
Afiliação
  • van der Loo LE; Department of Neurosurgery, Maastricht University Medical Centre, PO Box 5800, 6202, AZ, Maastricht, The Netherlands.
  • Beckervordersandforth J; Department of Pathology, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Colon AJ; Academic Centre for Epileptology, Kempenhaeghe/Maastricht University Medical Centre, Heeze, Maastricht, The Netherlands.
  • Schijns OE; Department of Neurosurgery, Maastricht University Medical Centre, PO Box 5800, 6202, AZ, Maastricht, The Netherlands. o.schijns@mumc.nl.
Acta Neurochir (Wien) ; 159(2): 397-400, 2017 02.
Article em En | MEDLINE | ID: mdl-27822901
We present the first and unique case of a rapid-growing skull hemangioma in a patient with Klippel-Trénaunay-Weber syndrome. This case report provides evidence that not all rapid-growing, osteolytic skull lesions need to have a malignant character but certainly need a histopathological verification. This material offers insight into the list of rare pathological diagnoses in an infrequent syndrome.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndrome de Klippel-Trenaunay-Weber / Hemangioma Limite: Female / Humans / Middle aged Idioma: En Revista: Acta Neurochir (Wien) Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndrome de Klippel-Trenaunay-Weber / Hemangioma Limite: Female / Humans / Middle aged Idioma: En Revista: Acta Neurochir (Wien) Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda