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- W3030106801 abstract "Objective To explore and summarize the clinical manifestations,iconographic characterizations,diagnosis and treatment principles of the type Ⅰ orbital neurofibromatosis.Methods Retrospectively reviewed the clinical features and imaging features including B-scan ultrasonography,Color doppler ultrasound (CDI),computed tomography (CT) and magnetic resonance imaging (MRI) of 43 patients with type Ⅰ neurofibromatosis,who were treated in our department from 2000 to 2010.Results Clinical features of the orbital type Ⅰ neurofibromatosis were often present at birth.The swelling of blepharon,ptosis,Lisch nodular and cafe-au-lait spots were the most common features.CT can showed the characteristic change of bones,such as the defects or dysplasia of the sphenoid,the enlargement of the orbital cavity and superior orbital fissure; MRI could better show the spread of tumor from the orbit to brain.Current treatment was heteropathy and operation was the main method.Conclusions The clinical features of the orbital type Ⅰ neurofibromatosis are various,the imaging examinations are useful for the differential diagnosis.Key words: Orbit; Neurofibromatosis; Clinical feature; Iconography" @default.
- W3030106801 created "2020-06-05" @default.
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- W3030106801 date "2012-12-10" @default.
- W3030106801 modified "2023-09-24" @default.
- W3030106801 title "Clinical analysis of the type I orbital neurofibromatosis" @default.
- W3030106801 doi "https://doi.org/10.3760/cma.j.issn.1006-4443.2012.12.026" @default.
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