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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease neurofibromatosis type 1
Symptom C0027830|neurofibromas
Sentences 26
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- 23035791 Background: to examine the natural growth dynamics of internal plexiform neurofibromas (pns) in patients with neurofibromatosis 1 (nf1).
PubMedID- 25289279 Summary: the resection of neurofibromas in von recklinghausen's disease neurofibromatosis type 1 (nf-1) is frequently complicated due to size, location, hypervascularity, and tissue friability.
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- 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- 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- 24189926 Comparative study of co2- and er:yag laser ablation of multiple cutaneous neurofibromas in von recklinghausen's disease.
PubMedID- 22593502 Vascular wall cells contribute to tumourigenesis in cutaneous neurofibromas of patients with neurofibromatosis type 1.
PubMedID- 21987445 Atypical neurofibromas in neurofibromatosis type 1 are premalignant tumors.
PubMedID- 21738979 To date, fewer than ten cases of subungual neurofibromas unassociated with von recklinghausen's disease have been documented, this being the first case to be reported in brazil and the only report worldwide to have described this condition in a male patient.
PubMedID- 23853192 Charcot-marie-tooth syndrome and neurofibromatosis type 1 with multiple neurofibromas of the entire spinal nerve roots.
PubMedID- 21525187 Different patterns of mast cells distinguish diffuse from encapsulated neurofibromas in patients 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- 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- 22112308 Background: the resection of neurofibromas in von recklinghausen's disease (nf-1) is frequently complicated by potentially life-threatening intraoperative and postoperative hemorrhage, due to the high tumor vascularity and tissue friability.
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- 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- 21999966 Bilateral spinal neurofibromas in patients with neurofibromatosis 1.
PubMedID- 23232267 We herein report the case of neurofibromatosis type 1 (nf-1) patient with bilateral neurofibromas originating from the mediastinal vagus just distal site of the recurrent nerve, who underwent two-staged extirpations that successfully preserved both recurrent nerves.
PubMedID- 23049566 neurofibromatosis type 1 presenting with plexiform neurofibromas in two patients: mri features.
PubMedID- 20010302 neurofibromatosis type 1 patients with plexiform neurofibromas are at risk of developing malignant peripheral nerve sheath tumors.
PubMedID- 23053586 Cervical myelopathy caused by bilateral c1-2 dumbbell ganglioneuromas and c2-3 and c3-4 neurofibromas associated with neurofibromatosis type 1.
PubMedID- 21415691 Resection of plexiform neurofibromas in children 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- 26282805 Dermoscopy of cutaneous neurofibromas associated with neurofibromatosis type 1.
PubMedID- 21621223 Plexiform neurofibromas in children with neurofibromatosis type 1: frequency and associated clinical deficits.

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