eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | neurofibromatosis type 1 |
| Comorbidity | C0027830|neurofibromas |
| Sentences | 28 |
| 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- 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- 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- 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- 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- 21525187 | Different patterns of mast cells distinguish diffuse from encapsulated neurofibromas in patients with neurofibromatosis 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- 21999966 | Bilateral spinal neurofibromas in patients with neurofibromatosis 1. |
| PubMedID- 26282805 | Dermoscopy of cutaneous neurofibromas associated with neurofibromatosis type 1. |
| 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- 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- 23853192 | Charcot-marie-tooth syndrome and neurofibromatosis type 1 with multiple neurofibromas of the entire spinal nerve roots. |
| PubMedID- 21586963 | These tumors arise from neurofibromas with or without von recklinghausen disease, and most of the remains develop from peripheral nerve trunks. |
| PubMedID- 23049566 | neurofibromatosis type 1 presenting with plexiform neurofibromas in two patients: mri features. |
| 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- 24860683 | The frequency of isolated neurofibromas unassociated with neurofibromatosis in the oral cavity is uncertain [3]. |
| 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- 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- 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- 21415691 | Resection of plexiform neurofibromas in children with neurofibromatosis type 1. |
| 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- 21621223 | Plexiform neurofibromas in children with neurofibromatosis type 1: frequency and associated clinical deficits. |
| 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- 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- 20010302 | neurofibromatosis type 1 patients with plexiform neurofibromas are at risk of developing malignant peripheral nerve sheath tumors. |
| PubMedID- 24189926 | Comparative study of co2- and er:yag laser ablation of multiple cutaneous neurofibromas in von recklinghausen's disease. |
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