• Lesions previously diagnosed as gastrointestinal (GI) neurofibromas in the NF1 population
are now recognised histologically to be GI stromal tumours (GISTs). 19, 20 NF1-associated …

Background: Neurofibromatosis type 1 (NF1) is a hereditary cancer predisposition syndrome
characterized by neurologic, dermatologic and orthopedic manifestations. There is a …

11035 Background: NF1 is an inherited autosomal dominant condition characterised by
multifocal neurofibromas, café au lait spots, Lisch nodules, freckling. GISTs are the most …

BACKGROUND Neurofibromatosis type 1 (NF1) is characterized by café-au-lait patches on
the skin and the presence of neurofibromas. Gastrointestinal stromal tumor (GIST) is the …

Neurofibromatosis type 1 is an autosomal dominant neurocutaneous disorder characterized
by a mutation of the neurofibromin 1 (NF1) gene, resulting in increased susceptibility for …

Abstract Background Type 1 neurofibromatosis (NF1) is a genetic tumor predisposing
Rasopathy. NF1 patients have an increased risk for developing benign and malignant …

Abstract Background Type 1 neurofibromatosis (NF1) is a genetic disease characterized by
neoplastic and not neoplastic disorders, involving tissues of neuroectodermal or …

Abstract Neurofibromatosis type 1 (NF1) is a genetic disorder associated with neurofibromin
1 (NF1) gene mutation, which generates an increased risk of variety of tumor types. The …

Abstract Background Neurofibromatosis type I (NF1) predisposes patients to various
neoplasias, including gastrointestinal stromal tumors (GISTs). Little is known about the risk …

Aims. The objectives of this study were (a) to report our experience regarding the
association between neurofibromatosis type 1 (NF1) and gastrointestinal stromal tumors …