Neurofibromatosis is an autosomal dominant genetic disease characterized by abnormal growth that involves tissues of mesodermal and neuroectodermal origin. Aneurysms are rarely seen in peripheral arteries. This report presents a case of ruptured arterial aneurysm secondary to neurofibromatosis; the lesion occurred in the profunda femoris artery, a highly unusual location. Treatment of patients with ruptured arterial aneurysm secondary to neurofibromatosis may be interventional or surgical. In this case, a surgical approach was successful. (Tex Heart Inst J 2010;37(3):368-70
Copyright © 2013 Brett Doleman et al. This is an open access article distributed under the Creative ...
A 38-year-old woman with neurofibromatosis type 1 was referred for massive swelling of the left thig...
The authors observed the spontaneous rupture of a dysplastic superficial femoral artery in a 47 year...
Neurofibromatosis is an autosomal dominant genetic disease characterized by abnormal growth that inv...
Neurofibromatosis is an autosomal dominant genetic disease characterized by abnormal growth that inv...
Neurofibromatosis is a dominantly inherited, progressive, generalized dysplasia of meso-dermal and n...
A 38-year-old woman with neurofibromatosis type 1 was referred for massive swelling of the left thig...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...
International audienceNeurofibromatosis type I (NFI), also called Von Recklinghausen disease, is an ...
International audienceNeurofibromatosis type I (NFI), also called Von Recklinghausen disease, is an ...
A 48-year-old woman with neurofibromatosis type 1 (NF1) experienced progressive forearm swelling cou...
Neurofibromatosis is a neurocutaneous genetic condition with dysplasia of the mesodermal and ectoder...
A 31-year-old woman with neurofibromatosis type I (NF-I) came to our hospital with hypotension and a...
Copyright © 2013 Brett Doleman et al. This is an open access article distributed under the Creative ...
A 38-year-old woman with neurofibromatosis type 1 was referred for massive swelling of the left thig...
The authors observed the spontaneous rupture of a dysplastic superficial femoral artery in a 47 year...
Neurofibromatosis is an autosomal dominant genetic disease characterized by abnormal growth that inv...
Neurofibromatosis is an autosomal dominant genetic disease characterized by abnormal growth that inv...
Neurofibromatosis is a dominantly inherited, progressive, generalized dysplasia of meso-dermal and n...
A 38-year-old woman with neurofibromatosis type 1 was referred for massive swelling of the left thig...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...
International audienceNeurofibromatosis type I (NFI), also called Von Recklinghausen disease, is an ...
International audienceNeurofibromatosis type I (NFI), also called Von Recklinghausen disease, is an ...
A 48-year-old woman with neurofibromatosis type 1 (NF1) experienced progressive forearm swelling cou...
Neurofibromatosis is a neurocutaneous genetic condition with dysplasia of the mesodermal and ectoder...
A 31-year-old woman with neurofibromatosis type I (NF-I) came to our hospital with hypotension and a...
Copyright © 2013 Brett Doleman et al. This is an open access article distributed under the Creative ...
A 38-year-old woman with neurofibromatosis type 1 was referred for massive swelling of the left thig...
The authors observed the spontaneous rupture of a dysplastic superficial femoral artery in a 47 year...