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[Symptomatic tumors in neurofibromatosis type 1: a diagnostic challenge]. / Symptomatische tumoren bij neurofibromatose type 1.
Taal, Walter; van Dijk, Sarah A; Noordhoek, Christine; Broen, Martijn P G; Gijtenbeek, J M M Anja; Oostenbrink, Rianne.
Afiliación
  • Taal W; Erasmus MC Kanker Instituut, ENCORE-NF1 expertise centrum, afd. Neurologie, Rotterdam.
  • van Dijk SA; Contact: Walter Taal (w.taal@erasmusmc.nl).
  • Noordhoek C; Erasmus MC Kanker Instituut, ENCORE-NF1 expertise centrum, afd. Neurologie, Rotterdam.
  • Broen MPG; Erasmus MC Kanker Instituut, ENCORE-NF1 expertise centrum, afd. Neurologie, Rotterdam.
  • Gijtenbeek JMMA; MUMC+, afd. Neurologie, Maastricht.
  • Oostenbrink R; Radboudumc, afd. Neurologie, Nijmegen.
Ned Tijdschr Geneeskd ; 1672023 11 22.
Article en Nl | MEDLINE | ID: mdl-37994710
Neurofibromatosis type 1 (NF1) is a hereditary, progressive and unpredictable disease, which can involve many organs. Benign and malignant tumors arise due to unrestrained cell division and cell growth. Recognizing the symptoms of these tumors and using the correct diagnostics is of great importance. In this clinical lesson we show the disease course of 3 patients with NF1. In all 3, the disease course was complicated by a symptomatic tumor. Characteristic in these patients is the relatively long interval between the onset of symptoms and the final tumor diagnosis. In this clinical lesson we examine the causes of this in more detail and we emphasize the importance of the specific knowledge within the Dutch national NF1 care network.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neurofibromatosis 1 Límite: Humans Idioma: Nl Revista: Ned Tijdschr Geneeskd Año: 2023 Tipo del documento: Article Pais de publicación: Países Bajos
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neurofibromatosis 1 Límite: Humans Idioma: Nl Revista: Ned Tijdschr Geneeskd Año: 2023 Tipo del documento: Article Pais de publicación: Países Bajos