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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease neurofibromatosis
Symptom C0027830|neurofibromas
Sentences 31
PubMedID- 21750756 Only one patient with primary neurofibromas associated with penile neurofibromatosis has been described to date in korea 6.
PubMedID- 22593502 Vascular wall cells contribute to tumourigenesis in cutaneous neurofibromas of patients with neurofibromatosis type 1.
PubMedID- 21415691 Resection of plexiform neurofibromas in children with neurofibromatosis type 1.
PubMedID- 23091673 Subtotal resection was performed with a small residual lesion in 6 tumors (27.3%), including 3 neurofibromatosis associated with brachial plexus neurofibromas, 1 mpnst and 2 granular cell tumor in one patient.
PubMedID- 24649470 The neurofibromas in neurofibromatosis type 1 are easily enhanced in the homogenous pattern.
PubMedID- 26282805 Dermoscopy of cutaneous neurofibromas associated with neurofibromatosis type 1.
PubMedID- 21999966 Bilateral spinal neurofibromas in patients with neurofibromatosis 1.
PubMedID- 22629013 1 solitary scrotal neurofibromas unassociated with neurofibromatosis type i (nf i) are extremely rare and to the best of our knowledge, only 10 cases have been reported in the english literature.
PubMedID- 22407214 The objective of this study was to investigate the predictive value of 18f-fluorodeoxyglucose positron emission tomography (fdg-pet) in detecting malignant transformation of plexiform neurofibromas in children with neurofibromatosis type 1 (nf1).
PubMedID- 24860683 The frequency of isolated neurofibromas unassociated with neurofibromatosis in the oral cavity is uncertain 3.
PubMedID- 22155606 8. eisenbarth, i., beyer, k., krone, w. and assum, g. (2000), 'toward a survey of somatic mutation of the nf1 gene in benign neurofibromas of patients with neurofibromatosis type 1', am.
PubMedID- 21987445 Atypical neurofibromas in neurofibromatosis type 1 are premalignant tumors.
PubMedID- 23862132 Mucosal schwann-cell hamartomas, which have no associations with inherited syndromes, have recently been categorized as a new disease to be distinguished from multiple neurofibromas associated with type-1 neurofibromatosis (nf1) 1.
PubMedID- 21188030 It is not clear exactly how often diffuse neurofibromas are associated with neurofibromatosis, although it has been suggested that about 10% of patients with diffuse neurofibromas have neurofibromatosis 1 (nf1, von recklinghausen’s disease).
PubMedID- 24681606 Malignant peripheral nerve sheath tumors (mpnsts) are soft tissue sarcomas that occur spontaneously, or from benign plexiform neurofibromas, in the context of the genetic disorder neurofibromatosis type 1 (nf1).
PubMedID- 21525187 Different patterns of mast cells distinguish diffuse from encapsulated neurofibromas in patients with neurofibromatosis 1.
PubMedID- 21621223 Plexiform neurofibromas in children with neurofibromatosis type 1: frequency and associated clinical deficits.
PubMedID- 23035791 Background: to examine the natural growth dynamics of internal plexiform neurofibromas (pns) in patients with neurofibromatosis 1 (nf1).
PubMedID- 23855960 Fibroblasts, mast cells and schwann cells were isolated from neurofibromas of patients with neurofibromatosis 1, and their responses to 308-nm excimer light irradiation and/or vitamin d3 or an analog (tacalcitol; 1,24-dihydroxyvitamin d3 ) were examined in vitro.
PubMedID- 22709421 Purpose: on occasion, neurofibromas in neurofibromatosis type 1 may be present on the lid, brow, or face of an infant or child, a circumstance commonly referred to as "orbitofacial neurofibromatosis" (ofnf).
PubMedID- 23598713 Purpose: the aim of this study was to analyze growth rate and identify prognostic factors for progression of postoperative plexiform neurofibromas in patients with neurofibromatosis type 1.
PubMedID- 24293303 In approximately 10 %, neurofibromas may be associated with neurofibromatosis (nf) 1 and 2. nf1 is commonly an autosomal dominant genetic disorder due to mutation of chromosome 17. in up to 50 % of patients, it can be a sporadic mutation.
PubMedID- 23853192 Charcot-marie-tooth syndrome and neurofibromatosis type 1 with multiple neurofibromas of the entire spinal nerve roots.
PubMedID- 25655626 (18)f-fdg pet/ct has shown increased accuracy, compared with morphologic imaging, in differentiating malignant peripheral nerve sheath tumors (mpnsts) from benign neurofibromas (bnfs) in patients with neurofibromatosis type 1 (nf1).
PubMedID- 23053586 Cervical myelopathy caused by bilateral c1-2 dumbbell ganglioneuromas and c2-3 and c3-4 neurofibromas associated with neurofibromatosis type 1.
PubMedID- 20680410 Plexiform neurofibromas commonly found in patients with neurofibromatosis type i (nf1) have a 5% risk of being transformed into malignant peripheral nerve sheath tumors (mpnst).
PubMedID- 20204131 Subcutaneous neurofibromas are usually associated with neurofibromatosis-1.
PubMedID- 23204034 We report the case of a 33-year-old male with multiple intrascrotal neurofibromas not associated with neurofibromatosis, treated by surgical excision.
PubMedID- 20520523 Nestin-positive stem cells in neurofibromas from patients with neurofibromatosis type 1-tumorigenic or incidental.
PubMedID- 23099009 Imatinib mesylate for plexiform neurofibromas in patients with neurofibromatosis type 1: a phase 2 trial.
PubMedID- 26463330 The cure rate of the neurofibromas with neurofibromatosis type 1 (nf1) and the neurofibromas without nf1 were 42.9% and 85.0%, respectively (p = 0.005).

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