Neurofibromatosis type 1 (NF1) is a tumor predisposition disease. Multiple neurofibromas are among the characteristic tumors of NF1. The report describes the diagnosis and treatment of a large spinal neurofibroma in a NF1 patient. The tumor showed a striking pigmentation and was diagnosed as pigmented (melanotic) neurofibroma. The distinction between this rare tumor variant and other pigmented tumors, especially malignant melanoma, is of primary importance.Die Neurofibromatose Typ 1 (NF1) ist eine Tumor-Prädispositionserkrankung. Multiple Neurofibrome zählen zu den charakteristischen Tumoren der NF1. Der Bericht beschreibt Diagnose und Behandlung eines ausgedehnten Neurofibroms des Rückens bei einem NF1 Patienten. Intraoperativ zeigte sich ...
Neurofibromatosis 1 (NF1) is an autosomal dominant disease. Neurofibromas, benign tumours that devel...
Neurofibromatosis is a genetic disorder of neural crest-derived cells that primarily affect growth o...
The common embryonic origin of neuroid and melanocytic cells justifies the simultaneous presence of ...
Neurofibromatoses (NF) are a group of genetic multiple tumor growing predisposition diseases: neurof...
Neurofibromatoses (NF) are a group of genetic multiple tumor growing predisposition diseases: neurof...
Neurofibromatosis type 1 (NF1) or Von Recklinghausen's disease is a dominantly inherited genetic, mu...
Neurofibromatosis (NF) belongs to the group of phakomatoses characterized by benign tumors of periph...
In the spectrum of neurofibromas, pigmented tumors are rare variants usually showing only faint, mac...
Neurofibromatosis type 1 (NF1) is an autosomal dominant neurocutaneous disorder, affecting approxima...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder, characterized by the development of benig...
Neurofibromatosis 1 (NF1) occurs in 1:2000 births. The main diagnostic signs are visible on the sk...
Neurofibromatosis type 1 (NF1) is a neurocutaneous condition with an autosomal dominant pattern of i...
Brief Introduction Neurofibromatosis type 1 (NF-1) is a multisystem neurocutaneous disorder resultin...
SummaryNeurofibromatosis type 1 is a relatively common inherited disorder. Patients have a high pred...
Neurofibromatosis type 1 is an autosomal dominant disease affecting one in 3000 to one in 4000 peopl...
Neurofibromatosis 1 (NF1) is an autosomal dominant disease. Neurofibromas, benign tumours that devel...
Neurofibromatosis is a genetic disorder of neural crest-derived cells that primarily affect growth o...
The common embryonic origin of neuroid and melanocytic cells justifies the simultaneous presence of ...
Neurofibromatoses (NF) are a group of genetic multiple tumor growing predisposition diseases: neurof...
Neurofibromatoses (NF) are a group of genetic multiple tumor growing predisposition diseases: neurof...
Neurofibromatosis type 1 (NF1) or Von Recklinghausen's disease is a dominantly inherited genetic, mu...
Neurofibromatosis (NF) belongs to the group of phakomatoses characterized by benign tumors of periph...
In the spectrum of neurofibromas, pigmented tumors are rare variants usually showing only faint, mac...
Neurofibromatosis type 1 (NF1) is an autosomal dominant neurocutaneous disorder, affecting approxima...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder, characterized by the development of benig...
Neurofibromatosis 1 (NF1) occurs in 1:2000 births. The main diagnostic signs are visible on the sk...
Neurofibromatosis type 1 (NF1) is a neurocutaneous condition with an autosomal dominant pattern of i...
Brief Introduction Neurofibromatosis type 1 (NF-1) is a multisystem neurocutaneous disorder resultin...
SummaryNeurofibromatosis type 1 is a relatively common inherited disorder. Patients have a high pred...
Neurofibromatosis type 1 is an autosomal dominant disease affecting one in 3000 to one in 4000 peopl...
Neurofibromatosis 1 (NF1) is an autosomal dominant disease. Neurofibromas, benign tumours that devel...
Neurofibromatosis is a genetic disorder of neural crest-derived cells that primarily affect growth o...
The common embryonic origin of neuroid and melanocytic cells justifies the simultaneous presence of ...