Neurofibromatosis type 2 (NF2) is an autosomal dominant condition caused by pathogenic variants in the NF2 gene. To date, cytotoxic chemotherapy has no established role in the treatment of NF-2. Historical case reports of malignant schwannomas have documented responses to chemotherapies with cyclophosphamide, vincristine and doxorubicin, in patients who develop pulmonary metastases. Recently, several studies proposed the use of anti-HER2, anti-EGFR, anti-platelet-derived growth factor receptors. As reported in our previous review of the literature, vascular endothelial growth factor (VEGF) and its receptor VEGFR-1 have been detected in schwannomas with the best results. We described the case of a young patient with NF2 treated for long time...
Background: NF2 patients develop multiple nervous system tumors including bilateral vestibular schwa...
Neurofibromatosis Type 1 (NF1) is an autosomal dominant tumor-predisposition disorder that is caused...
Neurofibromatosis type 1 (NF1) is a genetic multisystemic disorder involving the skin, the central a...
Neurofibromatosis type 2 (NF2) is an autosomal dominant condition caused by pathogenic variants in t...
Patients with bilateral vestibular schwannomas associated with neurofibromatosis type 2 (NF2) experi...
Neurofibromatosis type 2 (NF2) is an autoso-mal dominant syndrome with a prevalence of approximately...
Neurofibromatosis type 2 (NF2) patients develop multiple nervous system tumours including bilateral ...
Bevacizumab treatment can result in tumor shrinkage of progressive vestibular schwannomas in some ne...
Neurofibromatosis type 2 (NF2) is a debilitating disease characterized by the formation of bilateral...
Background: Neurofibromatosis type 1 (NF1) and neurofibromatosis type 2 (NF2) are rare tumoral suppr...
Neurofibromatosis type 2 is characterized by bilateral vestibular schwannomas, which are benign tumo...
A patient with neurofibromatosis type 2 (bilateral vestibular schwannomas) was treated with bevacizu...
Neurofibromatosis type 2 (NF2), a multiple neoplasia syndrome, is a manifestation of an impaired exp...
Neurofibromatosis type 1 (NF1) is a genetic disorder that carries a higher risk of tumor development...
Unlike adult neurofibromatosis type 2 (NF2), which presents with symptoms related to bilateral vesti...
Background: NF2 patients develop multiple nervous system tumors including bilateral vestibular schwa...
Neurofibromatosis Type 1 (NF1) is an autosomal dominant tumor-predisposition disorder that is caused...
Neurofibromatosis type 1 (NF1) is a genetic multisystemic disorder involving the skin, the central a...
Neurofibromatosis type 2 (NF2) is an autosomal dominant condition caused by pathogenic variants in t...
Patients with bilateral vestibular schwannomas associated with neurofibromatosis type 2 (NF2) experi...
Neurofibromatosis type 2 (NF2) is an autoso-mal dominant syndrome with a prevalence of approximately...
Neurofibromatosis type 2 (NF2) patients develop multiple nervous system tumours including bilateral ...
Bevacizumab treatment can result in tumor shrinkage of progressive vestibular schwannomas in some ne...
Neurofibromatosis type 2 (NF2) is a debilitating disease characterized by the formation of bilateral...
Background: Neurofibromatosis type 1 (NF1) and neurofibromatosis type 2 (NF2) are rare tumoral suppr...
Neurofibromatosis type 2 is characterized by bilateral vestibular schwannomas, which are benign tumo...
A patient with neurofibromatosis type 2 (bilateral vestibular schwannomas) was treated with bevacizu...
Neurofibromatosis type 2 (NF2), a multiple neoplasia syndrome, is a manifestation of an impaired exp...
Neurofibromatosis type 1 (NF1) is a genetic disorder that carries a higher risk of tumor development...
Unlike adult neurofibromatosis type 2 (NF2), which presents with symptoms related to bilateral vesti...
Background: NF2 patients develop multiple nervous system tumors including bilateral vestibular schwa...
Neurofibromatosis Type 1 (NF1) is an autosomal dominant tumor-predisposition disorder that is caused...
Neurofibromatosis type 1 (NF1) is a genetic multisystemic disorder involving the skin, the central a...