Literature DB >> 9693563

Neurofibromatosis of the orbit and skull base.

L Clauser1, F Carinci, M Galie.   

Abstract

Von Recklinghausen's disease is characterized by multiple neurofibromas, pigmentations, and pachydermatoceles of the skin depending on the disorder of the neural crest derivative. We report on a 25-year-old patient suffering from neurofibromatosis localized in the cranio-orbital region, whose main problem was a pulsating right exophthalmos caused by herniation of the frontotemporal lobe through a defect of the greater wing of the sphenoid. The lesion was approached through a combined route (i.e., transfrontally and transfacially [upper eyelid incision]). Surgical strategy and associated problems are discussed.

Entities:  

Mesh:

Year:  1998        PMID: 9693563     DOI: 10.1097/00001665-199805000-00020

Source DB:  PubMed          Journal:  J Craniofac Surg        ISSN: 1049-2275            Impact factor:   1.046


  3 in total

1.  Transcranial surgery through pterional approach for removal of cranio-orbital tumors by an interdisciplinary team of nurosurgeons and ophthalmologists.

Authors:  Yan Liu; Jiang-Rong Ma; Xue-Liang Xu
Journal:  Int J Ophthalmol       Date:  2012-04-18       Impact factor: 1.779

2.  Neuroimaging findings of extensive sphenoethmoidal dysplasia in NF1.

Authors:  Allison Tam; Joseph M Sliepka; Sunil Bellur; Collin Douglas Bray; Christie M Lincoln; Sandesh C S Nagamani
Journal:  Clin Imaging       Date:  2018-05-16       Impact factor: 1.605

3.  Partial thickness autologus calvarial bone orbitocranioplasty for a sphenorbital encephalocele presenting as pulsatile exophthalmos.

Authors:  Adarsh Trivedi; Amrish Kumar Garg; Subodh Hiran
Journal:  Asian J Neurosurg       Date:  2015 Apr-Jun
  3 in total

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