Results 91 to 100 of about 5,241 (204)

THE SURGICAL APPROACHES TO NASOPHARYNGEAL ANGIOFIBROMA

, 1994
After a short summary of the aetiopathogenesis, the routes of extension and the diagnostic features of nasopharyngeal angiofibroma, the importance of early diagnosis and careful surgical planning is underlined. In particular the extension and topographic
Francesco De Ponte, Roberto Delfini, CICCONETTI, Andrea, IANNETTI, Giorgio, BELLI, Evaristo   +4 more
core   +1 more source

Juvenile angiofibroma of skull base

, 2016
Nowadays, juvenile angiofibroma of skull base is one of the most complex and understudied problems of clinical and theoretical medicine. Angiofibroma of skull base occupied the leading position among the nasopharynx benign tumors.

core   +1 more source

Endoscopic sinus surgery for juvenile nasopharyngeal angiofibroma.

, 2000
Juvenile nasopharyngeal angiofibroma is a rare tumour of the head and neck with very specific characteristics: adolescent males, choana-nasopharynx, pterygomaxillary fossa widening, specific and intense vascularisation.
ROMBAUX, P, Bachert, C., Jorissen, M., Rombaux, Philippe, Daele, Jean-Michel, Bachert, Claus, DAELE, J, Bachert, ClausUGent8010012126589792689744360000-0003-4742-1665F5605D80-F0ED-11E1-A9DE-61C894A0A6B4, JORISSEN, M, ELOY, P, Eloy, Philippe   +10 more
core  

Nasopharyngeal Angiofibroma [PDF]

Ear, Nose & Throat Journal, 2008
Ryan, Kau, Mala, Tanna, Sasmita, Misra, Alejandro Luina, Contreras   +3 more
openaire   +2 more sources

Nasomaxillary Swing - A Novel Approach for Bilateral Angiofibroma

, 2009
Juvenile nasopharyngeal angiofibroma (JNA) is a high-risk tumor of adolescent males. Choice of the approach should be based on the stage and site of the lesion. For complete removal of tumor, surgical exposure must be adequate.
Alok Thakar, Gaurav Gupta, Mohnish Grover   +2 more
core   +1 more source

Tuberous sclerosis mimicking optic neuritis due to raised intracranial pressure: A diagnostic masquerade

Indian Journal of Ophthalmology. Case Reports
Tuberous sclerosis complex (TSC) is a rare phakomatosis with multisystem involvement. We report a 12-year-old girl with progressive bilateral vision loss, papilledema, and facial angiofibromas, initially suggestive of atypical optic neuritis.
Dhwanee Agarwal, Sukriti Gupta, Shreya Chandra, Harinder S Sethi   +3 more
doaj   +1 more source

Juvenile angiofibroma

, 2005
Juvenile angiofibroma is a rare, benign, rich vascular tumor, and approximately one new case is diagnosed in Denmark each year. It sits in the foramen sphenopalatinum and occurs in boys from 14 to 25 years of age.
Jakobsen, John, Nepper-Rasmussen, Jørgen, Thuesen, Anne Daugaard; id_orcid   +2 more
core   +1 more source

Spontaneous Involution of Nasopharyngeal Angiofibroma

, 2008
There are several studies addressing regression of residual nasopharyngeal angiofibroma after surgery, but spontaneous regression of this tumor has been reported in only 2 cases.
Onerci, Metin, Ugurel, Sahin, Tosun, Fuat, Durmaz, Abdullah   +3 more
core   +1 more source

Coblation-assisted endonasal endoscopic resection of juvenile nasopharyngeal angiofibroma

, 2011
Objective:Juvenile nasopharyngeal angiofibroma may be successfully resected using endoscopic techniques. However, the use of coblation technology for such resection has not been described.
J Li, L Ye, X Zhou, J Jin
core   +1 more source

Power Doppler findings in nasopharingeal angiofibroma

, 1998
Juvenile nasopharingeal angiofibroma (JNA) is a rare, histologically benign but clinically malign hypervascular tumor localized in the nasopharynx which occurs exclusively in adolescent boys. There is no definite attitude towards etiology of angiofibroma.
Sakarya, ME, Poyraz, N, Bozkurt, M, Arslan, H   +3 more
core   +1 more source