Introduction: Neurofibromatosis type 1 (NF-1) is an autosomal dominant disorder characterized by café-au-lait macules, neurofibromas, and iris hamartomas. Carotid artery aneurysms rarely affect patients with NF-1 but may be associated with rupture. We report the first episode of a ruptured external carotid aneurysm with severe life-threatening airway obstruction in a NF-1 patient. Presentation of case: We report a case of NF-1 32-year-old woman admitted to our department for life-threatening upper airway obstruction caused by spontaneous expanding swelling in the left sided neck. The diagnosis of ruptured aneurysm was suspected clinically and confirmed by computed tomography of the neck. The patient required tracheotomy for breathing diffic...
AbstractIntroductionIntrinsic lesions of the arterial wall are important manifestations of Neurofibr...
A 48-year-old woman with neurofibromatosis type 1 (NF1) experienced progressive forearm swelling cou...
Vasculopathy is a well-recognized abnormality associated with neurofibromatosis type 1(NF1) and may ...
AbstractIntroductionNeurofibromatosis type 1 (NF-1) is an autosomal dominant disorder characterized ...
AbstractIntroductionNeurofibromatosis type 1 (NF-1) is an autosomal dominant disorder characterized ...
SUMMARY: Although neurofibromatosis type 1 (NF-1) is commonly considered neurocutaneous, se-vere art...
Abstract Introduction Intrinsic lesions of the arterial wall are important manifestations of Neurofi...
Introduction: Vasculopathy, such as an aneurysm, stenosis, rupture, or arteriovenous fistula, in pat...
OBJECTIVE AND IMPORTANCE: We are sometimes involved in the care of patients with neurofibromatosis T...
AbstractIntroductionIntrinsic lesions of the arterial wall are important manifestations of Neurofibr...
AbstractINTRODUCTIONRupture of blood vessels associated with neurofibromatosis type 1 (NF-1) is a ra...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Neurofibromatosis is a neurocutaneous genetic condition with dysplasia of the mesodermal and ectoder...
AbstractIntroductionIntrinsic lesions of the arterial wall are important manifestations of Neurofibr...
A 48-year-old woman with neurofibromatosis type 1 (NF1) experienced progressive forearm swelling cou...
Vasculopathy is a well-recognized abnormality associated with neurofibromatosis type 1(NF1) and may ...
AbstractIntroductionNeurofibromatosis type 1 (NF-1) is an autosomal dominant disorder characterized ...
AbstractIntroductionNeurofibromatosis type 1 (NF-1) is an autosomal dominant disorder characterized ...
SUMMARY: Although neurofibromatosis type 1 (NF-1) is commonly considered neurocutaneous, se-vere art...
Abstract Introduction Intrinsic lesions of the arterial wall are important manifestations of Neurofi...
Introduction: Vasculopathy, such as an aneurysm, stenosis, rupture, or arteriovenous fistula, in pat...
OBJECTIVE AND IMPORTANCE: We are sometimes involved in the care of patients with neurofibromatosis T...
AbstractIntroductionIntrinsic lesions of the arterial wall are important manifestations of Neurofibr...
AbstractINTRODUCTIONRupture of blood vessels associated with neurofibromatosis type 1 (NF-1) is a ra...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Neurofibromatosis is a neurocutaneous genetic condition with dysplasia of the mesodermal and ectoder...
AbstractIntroductionIntrinsic lesions of the arterial wall are important manifestations of Neurofibr...
A 48-year-old woman with neurofibromatosis type 1 (NF1) experienced progressive forearm swelling cou...
Vasculopathy is a well-recognized abnormality associated with neurofibromatosis type 1(NF1) and may ...