A case report of neurofibromatosis
Authors
Abstract:
Introduction:Neurofibromatosis is a genetic disease characterized by multifocal benign tumors of peripheral nerves, called neurofibromas, and pigmented spots on the skin which inherited as autosomal-dominant. The most common form of the disease is neurofibromatosis type 1, also known as von Recklinghausen's disease of the skin. When an individual has small number of lesions in a limited region of the his body, it could be missed by the patient or not acknowledged by the clinicians as a form of neurofibromatosis. We present here, a case of an 18-year-old male with neurofibromatosis type 1who referred to Babol Dental School for a routine dental examination.
similar resources
A Rare Localization of Neurofibromatosis: A Case Report
Bericht einer seltenen Lokalisation der Neurofibromatose von Recklinghausen bei einem 6 jahrigen Madchen. In dieser publikation wurde zunachst die krankheit in kurzem besprochen und anschliesend ein intcressanter Fall mil exzeptionaler Lokalisation namlich Befall oberen Anteils des Mediastinums mit klinischem Bild einer akuten - Luftnot - situation vorgestellt. R·EFERENCES
full textOrbitotemporal Neurofibromatosis: Case Report
Plexiform neurofibromas occur in about 60% of neurofibromatosis type 1(NF-1) patients and can lead to severe morbidity by disfigurement or compression of vital structures. Moreover, these tumors can undergo malignant transformation. Both focal and localized bone abnormalities are part of the phenotypic expression of NF-1. We report a rare case of severe cranioorbital plexiform neurofibromatosis...
full textSegmental Neurofibromatosis Type 1, a Rare Variant of Neurofibromatosis: Report of Two Cases
Segmental neurofibromatosis type I (SNF-I) is a rare variant of neurofibromatosis (NF). It is classified as NF type V and defined as cafe'-au-lait macules and/or neurofibromas in a single ,unilateral segment of the body .We report two cases with SNF-I with striking similar manifestations.
full textA Large Intrathoracic Mass in a Patient with Neurofibromatosis-1: a case report
Abstracts: Dural ectasia is circumferential expansion or dilatation of the dural sac, and has been frequently reported in association with type 1 neurofibromatosis (NF1). It should be differentiated from posterior mediastinal tumors such as neurofibroma, neuroblastoma, and ganglioneuroma because NF-1 has a high risk of tumor formation. In the spinal deformities of NF-1 patients, despite the sco...
full textHypertension and neurofibromatosis. Case report.
A 14-year-old girl with neurofibromatosis presented with severe hypertension. She was subsequently found to have a cerebellar glioblastoma multiforme and vascular lesions producing coarctation of the abdominal aorta and 50% and 95% stenosis of the left and right renal arteries respectively. No evidence of pheochromocytoma was found. After removal of the cerebellar tumor, marked amelioration of ...
full textPrimary prostate solitary neurofibroma without neurofibromatosis-I: a case report and narrative review of the literature
Neurofibroma of the prostate is an extremely rare benign tumor, particularly when it is not associated with neurofibromatosis-I (NF-1). This study aimed to report the case of a 44-year-old man who presented with dysuria for about 4 years. Magnetic resonance imaging (MRI) showed a mass in the prostate with “target sign” on T2-weighted imaging. The mass was surgically excised, and histopathologic...
full textMy Resources
Journal title
volume 3 issue None
pages 47- 51
publication date 2014-03
By following a journal you will be notified via email when a new issue of this journal is published.
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023