| Literature DB >> 16549958 |
Omer Onbas1, Cihangir Aliagaoglu, Cagatay Calikoglu, Mecit Kantarci, Mustafa Atasoy, Fatih Alper.
Abstract
Neurofibromatosis type 1 disease is characterized by pigmented cutaneous lesions and generalized tumors of a neural crest origin and it may affect all the systems of the human body. Sphenoid dysplasia is one of the characteristics of this syndrome and it occurs in 5-10% of the cases; further, abnormalities of the sphenoid wings are often considered pathognomonic. However, complete agenesis of a sphenoid wing is very rare. We report here on an unusual case of neurofibromatosis type 1 disease with the associated absence of a sphenoid wing that was diagnosed by using multidetector computed tomography.Entities:
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Year: 2006 PMID: 16549958 PMCID: PMC2667581 DOI: 10.3348/kjr.2006.7.1.70
Source DB: PubMed Journal: Korean J Radiol ISSN: 1229-6929 Impact factor: 3.500