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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease neurofibroma
Comorbidity C0085113|neurofibromatosis
Sentences 42
PubMedID- 24860683 The plexiform variant of neurofibroma associated with neurofibromatosis i seems to have a significant increased incidence of malignant transformation when compared to other variants [3].
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- 22593502 Vascular wall cells contribute to tumourigenesis in cutaneous neurofibromas of patients with neurofibromatosis type 1.
PubMedID- 24751814 Hybrid perineurioma-neurofibroma in a patient with neurofibromatosis type 1, clinically mimicking malignant peripheral nerve sheath tumor.
PubMedID- 21525187 Different patterns of mast cells distinguish diffuse from encapsulated neurofibromas in patients with neurofibromatosis 1.
PubMedID- 23351479 Although abnormal gag reflexes have been reported in cases of glossopharyngeal schwannoma and neurofibroma in patients with neurofibromatosis-1, a gag reflex has not been reported previously as a complication of im in the head and neck.
PubMedID- 23091673 Subtotal resection was performed in 6 tumors (27.3%), including 3 neurofibromatosis associated with brachial plexus neurofibromas, 1 mpnst and 2 granular cell tumor in one patient.
PubMedID- 24492891 Spontaneous hip dislocation due to intraarticular neurofibroma in patients with neurofibromatosis type 1 is extremely rare.
PubMedID- 24007690 Approximately one-half of malignant peripheral nerve sheath tumors arise from a benign peripheral nerve sheath tumor, which is commonly a neurofibroma in patients with neurofibromatosis type 1.
PubMedID- 26282805 Dermoscopy of cutaneous neurofibromas associated with neurofibromatosis type 1.
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- 22145517 Isolated orbital neurofibroma unassociated with systemic neurofibromatosis is relatively rare and may be difficult to clinically differentiate from other orbital tumors.
PubMedID- 21999966 We present 8 patients (5 m and 3 f) with sporadic or non-familial spinal neurofibromatosis 1 (non-fsnf1) associated with bilateral spinal neurofibromas involving all of the paraspinal nerves.
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- 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).
PubMedID- 23061950 The deformity was caused by a neurofibroma associated with neurofibromatosis type 1, affecting the left ring finger.
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- 24321536 Puberty and plexiform neurofibroma tumor growth in patients with neurofibromatosis type i.
PubMedID- 23099009 Imatinib mesylate for plexiform neurofibromas in patients with neurofibromatosis type 1: a phase 2 trial.
PubMedID- 20520523 Nestin-positive stem cells in neurofibromas from patients with neurofibromatosis type 1-tumorigenic or incidental.
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- 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- 23204034 We report the case of a 33-year-old male with multiple intrascrotal neurofibromas not associated with neurofibromatosis, treated by surgical excision.
PubMedID- 24472086 Cutaneous epithelioid melanocytic neurofibroma arising in a patient with neurofibromatosis-1.
PubMedID- 21750756 neurofibromas are often associated with neurofibromatosis type 1 (nf1) or von recklinghausen disease, and a plexiform neurofibroma of the penis associated with erectile dysfunction has been described [4].
PubMedID- 22593511 Size of tooth crowns and position of teeth concerning the extension of facial plexiform neurofibroma in patients with neurofibromatosis type 1.
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- 24656164 Co-occurrence of choroidal pigmented ganglioneuroma and plexiform neurofibroma in a patient with neurofibromatosis 1.
PubMedID- 20212235 Giant plexiform neurofibroma in neurofibromatosis type 1.
PubMedID- 23853192 Charcot-marie-tooth syndrome and neurofibromatosis type 1 with multiple neurofibromas of the entire spinal nerve roots.
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- 21415691 Resection of plexiform neurofibromas in children with neurofibromatosis type 1.
PubMedID- 23053586 Cervical myelopathy caused by bilateral c1-2 dumbbell ganglioneuromas and c2-3 and c3-4 neurofibromas associated with neurofibromatosis type 1.
PubMedID- 22506209 The histopathology revealed that both cases had undergone malignant transformation from plexiform neurofibroma in patients with neurofibromatosis type 1 (nf1).
PubMedID- 20077367 Cervical segment nervus vagus neurofibroma with associated neurofibromatosis type 1: a case report.
PubMedID- 23922330 Malignant degeneration frequently arises from preexisting plexiform neurofibroma in patients with neurofibromatosis type 1 (nf1).
PubMedID- 22419190 We reviewed and characterized surgically resected cases of intrapulmonary neurofibroma without neurofibromatosis type 1 especially in comparison with cases of endotracheobronchial neurofibroma.
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- 21987445 Atypical neurofibromas in neurofibromatosis type 1 are premalignant tumors.
PubMedID- 26361430 Perforated appendiceal diverticulitis associated with appendiceal neurofibroma in neurofibromatosis type 1.
PubMedID- 20204131 Subcutaneous neurofibromas are usually associated with neurofibromatosis-1.

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