A CASE OF NEUROFIBROMATOSIS TYPE 1

Neurofibromatosis (NF) is a term that has been applied to a variety of related syndromes, characterized by neuroectodermal tumors arising within multiple organs and autosomal-dominant inheritance. Neurofibromatosis type I (NF-1), known as well as Recklinghausen's disease, is the most common typ...

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Main Authors: Valentina Dimitrova (Author), Ivelina Yordanova (Author), Verka Pavlova (Author), Valentin Valtchev (Author), Dimitar Gospodinov (Author), Boryana Parashkevova (Author), Chavdar Balabanov (Author)
Format: Book
Published: Peytchinski Publishing, 2008-10-01T00:00:00Z.
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Summary:Neurofibromatosis (NF) is a term that has been applied to a variety of related syndromes, characterized by neuroectodermal tumors arising within multiple organs and autosomal-dominant inheritance. Neurofibromatosis type I (NF-1), known as well as Recklinghausen's disease, is the most common type of the disease accounting 90% of the cases. We present a case of 52-year-old men with NF-1. The disease started in childhood with the appearance of multiple hyperpigmented skin macules. At the age of 46 a lot of cutaneous tumors appeared and started growing bigger all over the body surface. Because of a vision problem due to an upper left eyelid neurofibroma, the patient came for a clinical examination at the age of 52 years.
Item Description:10.5272/jimab.14-1-2010.63
1312-773X