Neurofibromatosis (NF) is a relatively common disorder characterized by cutaneous pigmented maculas, multiple neurofibromas and Lisch nodules (pigmented iris hamartomas). This disorder is retained being a neurocristopathy. Melanocytes are neural crest derivates too. Twenty-six patients with neurofibromatosis associated to cutaneous malignant melanoma have been reported till now, but data on association between these two pathologies are lacking. One more case of malignant cutaneous melanoma in a patient with neurofibromatosis is reported and the hypothesis of a more frequent association than usually believed of these two pathologies is discussed
Neurofibromatosis I (NF I), an autosomal dominant disorder is associated with increased risk of beni...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder, characterized by the development of benig...
Neurofibromatosis-1 (NF1) is one of the most common hereditary multisystemic disorders. The disease ...
Neurofibromatosis type 1 (NF1) is an autosomal dominant neurocutaneous disorder, affecting approxima...
Neurofibromatosis type 1 (NF1) is a tumor predisposition disease. Multiple neurofibromas are among t...
The common embryonic origin of neuroid and melanocytic cells justifies the simultaneous presence of ...
Neurofibromatosis 1 (NF1) occurs in 1:2000 births. The main diagnostic signs are visible on the sk...
Objective. To better understand the real prevalence of cutaneous manifestations, in Neurofibromatosi...
peer reviewedMajor syndromes in which cutaneous and extracutaneous nervous neoplasms are frequently ...
Background: Neurofibromatosis type 1 (NF1) is a cancer syndrome associated with many different cance...
An unusual case of melanotic neurofibroma which involves subcutaneous tissue and dura in the occipit...
In the spectrum of neurofibromas, pigmented tumors are rare variants usually showing only faint, mac...
Neurofibromatosis-1 (NF-1) is a neuroectodermal abnormality characterized by multiple neurofibromas,...
In the spectrum of neurofibromas, pigmented tumors are rare variants usually showing only faint, mac...
Neurofibromatosis type 1 (NF1) is a common genetic disease whose dermatological lesions are at the f...
Neurofibromatosis I (NF I), an autosomal dominant disorder is associated with increased risk of beni...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder, characterized by the development of benig...
Neurofibromatosis-1 (NF1) is one of the most common hereditary multisystemic disorders. The disease ...
Neurofibromatosis type 1 (NF1) is an autosomal dominant neurocutaneous disorder, affecting approxima...
Neurofibromatosis type 1 (NF1) is a tumor predisposition disease. Multiple neurofibromas are among t...
The common embryonic origin of neuroid and melanocytic cells justifies the simultaneous presence of ...
Neurofibromatosis 1 (NF1) occurs in 1:2000 births. The main diagnostic signs are visible on the sk...
Objective. To better understand the real prevalence of cutaneous manifestations, in Neurofibromatosi...
peer reviewedMajor syndromes in which cutaneous and extracutaneous nervous neoplasms are frequently ...
Background: Neurofibromatosis type 1 (NF1) is a cancer syndrome associated with many different cance...
An unusual case of melanotic neurofibroma which involves subcutaneous tissue and dura in the occipit...
In the spectrum of neurofibromas, pigmented tumors are rare variants usually showing only faint, mac...
Neurofibromatosis-1 (NF-1) is a neuroectodermal abnormality characterized by multiple neurofibromas,...
In the spectrum of neurofibromas, pigmented tumors are rare variants usually showing only faint, mac...
Neurofibromatosis type 1 (NF1) is a common genetic disease whose dermatological lesions are at the f...
Neurofibromatosis I (NF I), an autosomal dominant disorder is associated with increased risk of beni...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder, characterized by the development of benig...
Neurofibromatosis-1 (NF1) is one of the most common hereditary multisystemic disorders. The disease ...