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Neurofibromatosis type 1 adult surveillance form for Austria.
Sunder-Plassmann, Vincent; Azizi, Amedeo A; Farschtschi, Said; Gruber, Robert; Hutterer, Markus; Ladurner, Viktoria; Röhl, Claas; Welponer, Tobias; Bergmeister-Berghoff, Anna-Sophie.
Afiliación
  • Sunder-Plassmann V; Division of Oncology, Department of Medicine I, Medical University of Vienna, Waehringer Gürtel 18-20, 1090, Vienna, Austria. vincent.sunder-plassmann@meduniwien.ac.at.
  • Azizi AA; Christian Doppler Laboratory for Personalized Immunotherapy, Department of Medicine I, Medical University of Vienna, Vienna, Austria. vincent.sunder-plassmann@meduniwien.ac.at.
  • Farschtschi S; Division of Neonatology, Pediatric Intensive Care and Neuropediatrics, Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.
  • Gruber R; Comprehensive Center for Pediatrics, Medical University of Vienna, Vienna, Austria.
  • Hutterer M; Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
  • Ladurner V; International Center for Neurofibromatoses, Department of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg-Eppendorf, Germany.
  • Röhl C; Department of Dermatology, Venereology and Allergy, Medical University of Innsbruck, Innsbruck, Austria.
  • Welponer T; Department of Neurology with Acute Geriatrics, Saint John of God Hospital Linz, Linz, Austria.
  • Bergmeister-Berghoff AS; Department of Neurology, Hospital of Villach, Villach, Austria.
Wien Klin Wochenschr ; 2024 Sep 12.
Article en En | MEDLINE | ID: mdl-39264447
ABSTRACT

BACKGROUND:

Neurofibromatosis type 1 (NF1) is a rare autosomal dominant tumor predisposition syndrome with a birth prevalence of approximately 1 in 2000-3000 individuals. Management of both benign and malignant tumors arising in individuals with NF1 is demanding and tumors may be difficult to treat. Both standardized and individual surveillance programs are therefore highly important to prevent morbidity and mortality in patients with NF1.

METHODS:

The guidelines for the clinical management of NF1 recently proposed by the European Reference Network for Genetic Tumor Risk Syndromes provide the cornerstone of the present surveillance form and were discussed through three rounds of voting and a final consensus meeting involving experts from five Austrian and one German clinical NF1 centers for adults and one patient organization representative. Subsequently, 31 items within 4 categories were integrated into the proposed surveillance form for Austria. All recommendations, unless otherwise specified, pertain to primarily asymptomatic patients in routine follow-up.

RECOMMENDATIONS:

At healthcare transition from pediatric to adult surveillance or the initial visit in adulthood, we suggest a thorough clinical, laboratory and radiological examination to obtain a baseline for future diagnostics. To comply with the general screening recommendations in Austria, we suggest extending the frequency of clinical visits from annual to biennial at 50 years of age. In cases of clinical dynamics, early follow-up is recommended to facilitate early detection of potential complications. Particular emphasis should be placed on preventive patient education.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Wien Klin Wochenschr Año: 2024 Tipo del documento: Article País de afiliación: Austria Pais de publicación: Austria

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Wien Klin Wochenschr Año: 2024 Tipo del documento: Article País de afiliación: Austria Pais de publicación: Austria